ORGANIC LIGHT-EMITTING MATERIALS CONTAINING CYANO-SUBSTITUTED LIGAND

Abstract

An organic light-emitting material containing cyano-substituted ligand is disclosed. The organic light-emitting material is a metal complex containing a cyano-substituted ligand, which can be used as a light-emitting material in a light-emitting layer of an organic electroluminescent device. These new complexes can provide better device performance, e.g., narrower full width at half maximum, lower voltage values, and higher quantum efficiency, and the like. An electroluminescent device and a compound formulation containing the metal complex, and a compound capable of being used to prepare the metal complex are also disclosed.

Description

This application is a continuation application of U.S. application Ser. No. 16/750,282 titled “ORGANIC LIGHT-EMITTING MATERIALS CONTAINING A CYANO-SUBSTITUTED LIGAND” filed on Jan. 23, 2020, which claims priority to Chinese Patent Application No. 201910077079.0 filed on Feb. 1, 2019, and the entirety of each of which is incorporated herein by reference.

TECHNICAL FIELD

The present disclosure relates to a compound for using in an organic electronic device, such as an organic light-emitting device. In particular, it relates to a metal complex containing a cyano-substituted ligand, and an electroluminescent device and a compound formulation containing the metal complex.

BACKGROUND

Organic electronic devices include, but are not limited to, the following types: organic light-emitting diodes (OLEDs), organic field-effect transistors (O-FETs), organic light-emitting transistors (OLETs), organic photovoltaic devices (OPVs), dye-sensitized solar cells (DSSCs), organic optical detectors, organic photoreceptors, organic field-quench devices (OFQDs), light-emitting electrochemical cells (LECs), organic laser diodes and organic plasmon emitting devices.

In 1987, Tang and Van Slyke of Eastman Kodak reported a bilayer organic electroluminescent device, which comprises an arylamine hole transporting layer and a tris-8-hydroxyquinolato-aluminum layer as the electron and emitting layer (Applied Physics Letters, 1987, 51 (12): 913-915). Once a bias is applied to the device, green light was emitted from the device. The present disclosure laid the foundation for the development of modem organic light-emitting diodes (OLEDs). State-of-the-art OLEDs may comprise multiple layers such as charge injection and transporting layers, charge and exciton blocking layers, and one or multiple emissive layers between the cathode and anode. Since OLED is a self-emitting solid state device, it offers tremendous potential for display and lighting applications. In addition, the inherent properties of organic materials, such as their flexibility, may make them well suited for particular applications such as fabrication on flexible substrates.

OLED can be categorized as three different types according to its emitting mechanism. The OLED invented by Tang and van Slyke is a fluorescent OLED. It only utilizes singlet emission. The triplets generated in the device are wasted through nonradiative decay channels. Therefore, the internal quantum efficiency (IQE) of a fluorescent OLED is only 25%. This limitation hindered the commercialization of OLED. In 1997, Forrest and Thompson reported phosphorescent OLED, which uses triplet emission from heave metal containing complexes as the emitter. As a result, both singlet and triplets can be harvested, achieving 100% IQE. The discovery and development of phosphorescent OLED contributed directly to the commercialization of active-matrix OLED (AMOLED) due to its high efficiency. Recently, Adachi achieved high efficiency through thermally activated delayed fluorescence (TADF) of organic compounds. These emitters have small singlet-triplet gap that makes the transition from triplet back to singlet possible. In the TADF device, the triplet excitons can go through reverse intersystem crossing to generate singlet excitons, resulting in high IQE.

OLEDs can also be classified as small molecule and polymer OLEDs according to the forms of the materials used. Small molecule refers to any organic or organometallic material that is not a polymer. The molecular weight of a small molecule can be large as long as it has well defined structure. Dendrimers with well-defined structures are considered as small molecules.

Polymer OLEDs include conjugated polymers and non-conjugated polymers with pendant emitting groups. Small molecule OLED can become a polymer OLED if post polymerization occurred during the fabrication process.

There are various methods for OLED fabrication. Small molecule OLEDs are generally fabricated by vacuum thermal evaporation. Polymer OLEDs are fabricated by solution process such as spin-coating, inkjet printing, and slit printing. If the material can be dissolved or dispersed in a solvent, the small molecule OLED can also be produced by solution process.

The emitting color of an OLED can be achieved by emitter structural design. An OLED may comprise one emitting layer or a plurality of emitting layers to achieve desired spectrum. In the case of green, yellow, and red OLEDs, phosphorescent emitters have successfully reached commercialization. Blue phosphorescent device still suffers from non-saturated blue color, short device lifetime, and high operating voltage. Commercial full-color OLED displays normally adopt a hybrid strategy, using fluorescent blue and phosphorescent yellow, or red and green. At present, efficiency roll-off of phosphorescent OLEDs at high brightness remains a problem. In addition, it is desirable to have more saturated emitting color, higher efficiency, and longer device lifetime.

Cyano substitution is not often introduced into phosphorescent metal complexes, such as iridium complexes. US20140252333A1 discloses a series of iridium complexes substituted with cyano-phenyl, and as a result, the effect brought by the cyano group is not clearly indicated. In addition, since the cyano group is a very electron-withdrawing substituent, it is also used to blue-shift the emission spectrum of phosphorescent metal complexes, such as disclosed in US20040121184A1.

SUMMARY

The present disclosure aims to provide a series of technical solutions to solve at least part of the above problems.

One object of the present disclosure is to provide a metal complex comprising a ligand La represented by Formula 1:

• • wherein, Cy is a substituted or unsubstituted aryl or heteroaryl group having 5 to 24 ring atoms;
  • wherein, Cy is connected to a metal through a metal-carbon bond or a metal-nitrogen bond;
  • wherein, X₁ to X₄ are each independently selected from C, CR_x1 or N, and at least one of X₁ to X₄ is C and connected to Cy; when more than one of X₁ to X₄ is CR_x1, the R_x1 may be the same or different;
  • wherein, X₅ to X₈ are each independently selected from CR_x2 or N; when more than one of X₅ to X₈ is CR_x2, the R_x2 may be the same or different;
  • wherein, X is selected from the group consisting of O, S, Se, NR_x3, CR_x4R_x5 and SiR_x6R_x7;
  • wherein, R_x1, R_x2, R_x3, R_x4, R_x5, R_x6 and R_x7 are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted arylalkyl group having 7-30 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted aryloxy group having 6-30 carbon atoms, a substituted or unsubstituted alkenyl group having 2-20 carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a substituted or unsubstituted arylsilyl group having 6-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof,
  • wherein, at least one of R_x1 and R_x2 is a cyano group;
  • any two adjacent substituents can optionally be joined to form a ring;
  • X₁, X₂, X₃ or X₄ is connected to the metal through a metal-carbon bond or a metal-nitrogen bond.

A second object of the present disclosure is to provide an electroluminescent device, which includes an anode, a cathode, and an organic layer disposed between the anode and the cathode, wherein the organic layer comprises the metal complex according to the first object of the present disclosure.

A third object of the present disclosure is to provide a compound formulation, which comprises the metal complex according to the first object of the present disclosure.

A fourth object of the present disclosure is to provide a compound that can be used for preparing the metal complex according to the first object of the present disclosure.

The novel metal complex having a cyano-substituted ligand disclosed by the present disclosure can be used as a light-emitting material in an electroluminescent device. When used in electroluminescent devices, these novel compounds can provide better device performance, e.g., narrower full width at half maximum, lower voltage values, and higher quantum efficiency, and the like.

The present invention discloses a series of novel cyano-substituted metal complexes which unexpectedly show many characteristics, such as high efficiency, low voltage, and no obvious blue-shifted or red-shifted luminescence. The most unexpected is that they have a very narrow peak width of emitted light. These advantages will greatly help to improve the level and color saturation of green light devices.

DESCRIPTION OF DRAWINGS

FIG. 1 is a schematic diagram of an organic light-emitting device that may contain a metal complex and a compound formulation disclosed herein.

FIG. 2 is a schematic diagram of another organic light-emitting device that may contain a metal complex and a compound formulation disclosed herein.

FIG. 3 is a diagram showing a ligand L_a represented by Formula 1 as disclosed herein.

DETAILED DESCRIPTION

OLEDs can be fabricated on various types of substrates such as glass, plastic, and metal foil. FIG. 1 schematically shows the organic light emitting device 100 without limitation. The figures are not necessarily drawn to scale. Some of the layers in the figures can also be omitted as needed. Device 100 may include a substrate 101, an anode 110, a hole injection layer 120, a hole transport layer 130, an electron blocking layer 140, an emissive layer 150, a hole blocking layer 160, an electron transport layer 170, an electron injection layer 180 and a cathode 190. Device 100 may be fabricated by depositing the layers described in order. The properties and functions of these various layers, as well as example materials, are described in more detail in U.S. Pat. No. 7,279,704 at cols. 6-10, the contents of which are incorporated by reference herein in its entirety.

More examples for each of these layers are available. For example, a flexible and transparent substrate-anode combination is disclosed in U.S. Pat. No. 5,844,363, which is incorporated by reference herein in its entirety. An example of a p-doped hole transport layer is m-MTDATA doped with F₄-TCNQ at a molar ratio of 50:1, as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference herein in its entirety. Examples of host materials are disclosed in U.S. Pat. No. 6,303,238 to Thompson et al., which is incorporated by reference herein in its entirety. An example of an n-doped electron transport layer is BPhen doped with Li at a molar ratio of 1:1, as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference herein in its entirety. U.S. Pat. Nos. 5,703,436 and 5,707,745, which are incorporated by reference herein in their entireties, disclose examples of cathodes including composite cathodes having a thin layer of metal such as Mg:Ag with an overlying transparent, electrically-conductive, sputter-deposited ITO layer. The theory and use of blocking layers is described in more detail in U.S. Pat. No. 6,097,147 and U.S. Patent Application Publication No. 2003/0230980, which are incorporated by reference herein in their entireties. Examples of injection layers are provided in U.S. Patent Application Publication No. 2004/0174116, which is incorporated by reference herein in its entirety. A description of protective layers may be found in U.S. Patent Application Publication No. 2004/0174116, which is incorporated by reference herein in its entirety.

The layered structure described above is provided by way of non-limiting example. Functional OLEDs may be achieved by combining the various layers described in different ways, or layers may be omitted entirely. It may also include other layers not specifically described. Within each layer, a single material or a mixture of multiple materials can be used to achieve optimum performance. Any functional layer may include several sublayers. For example, the emissive layer may have two layers of different emitting materials to achieve desired emission spectrum.

In one embodiment, an OLED may be described as having an “organic layer” disposed between a cathode and an anode. This organic layer may comprise a single layer or multiple layers.

An OLED can be encapsulated by a barrier layer. FIG. 2 schematically shows the organic light emitting device 200 without limitation. FIG. 2 differs from FIG. 1 in that the organic light emitting device include a barrier layer 102, which is above the cathode 190, to protect it from harmful species from the environment such as moisture and oxygen. Any material that can provide the barrier function can be used as the barrier layer such as glass and organic-inorganic hybrid layers. The barrier layer should be placed directly or indirectly outside of the OLED device. Multilayer thin film encapsulation was described in U.S. Pat. No. 7,968,146, which is herein incorporated by reference in its entirety.

Devices fabricated in accordance with embodiments of the present disclosure can be incorporated into a wide variety of consumer products that have one or more of the electronic component modules (or units) incorporated therein. Some examples of such consumer products include flat panel displays, monitors, medical monitors, televisions, billboards, lights for interior or exterior illumination and/or signaling, heads-up displays, fully or partially transparent displays, flexible displays, smart phones, tablets, phablets, wearable devices, smart watches, laptop computers, digital cameras, camcorders, viewfinders, micro-displays, 3-D displays, vehicles displays, and vehicle tail lights.

The materials and structures described herein may be used in other organic electronic devices listed above.

As used herein, “top” means furthest away from the substrate, while “bottom” means closest to the substrate. Where a first layer is described as “disposed over” a second layer, the first layer is disposed further away from substrate. There may be other layers between the first and second layer, unless it is specified that the first layer is “in contact with” the second layer. For example, a cathode may be described as “disposed over” an anode, even though there are various organic layers in between.

As used herein, “solution processible” means capable of being dissolved, dispersed, or transported in and/or deposited from a liquid medium, either in solution or suspension form.

A ligand may be referred to as “photoactive” when it is believed that the ligand directly contributes to the photoactive properties of an emissive material. A ligand may be referred to as “ancillary” when it is believed that the ligand does not contribute to the photoactive properties of an emissive material, although an ancillary ligand may alter the properties of a photoactive ligand.

It is believed that the internal quantum efficiency (IQE) of fluorescent OLEDs can exceed the 25% spin statistics limit through delayed fluorescence. As used herein, there are two types of delayed fluorescence, i.e. P-type delayed fluorescence and E-type delayed fluorescence. P-type delayed fluorescence is generated from triplet-triplet annihilation (TTA).

On the other hand, E-type delayed fluorescence does not rely on the collision of two triplets, but rather on the transition between the triplet states and the singlet excited states. Compounds that are capable of generating E-type delayed fluorescence are required to have very small singlet-triplet gaps to convert between energy states. Thermal energy can activate the transition from the triplet state back to the singlet state. This type of delayed fluorescence is also known as thermally activated delayed fluorescence (TADF). A distinctive feature of TADF is that the delayed component increases as temperature rises. If the reverse intersystem crossing rate is fast enough to minimize the non-radiative decay from the triplet state, the fraction of back populated singlet excited states can potentially reach 75%. The total singlet fraction can be 100%, far exceeding 25% of the spin statistics limit for electrically generated excitons.

E-type delayed fluorescence characteristics can be found in an exciplex system or in a single compound. Without being bound by theory, it is believed that E-type delayed fluorescence requires the luminescent material to have a small singlet-triplet energy gap (ΔE_S-T). Organic, non-metal containing, donor-acceptor luminescent materials may be able to achieve this. The emission in these materials is often characterized as a donor-acceptor charge-transfer (CT) type emission. The spatial separation of the HOMO and LUMO in these donor-acceptor type compounds often results in small ΔE_S-T. These states may involve CT states. Often, donor-acceptor luminescent materials are constructed by connecting an electron donor moiety such as amino- or carbazole-derivatives and an electron acceptor moiety such as N-containing six-membered aromatic rings.

Definition of Terms of Substituents

Halogen or halide—as used herein includes fluorine, chlorine, bromine, and iodine.

Alkyl—contemplates both straight and branched chain alkyl groups. Examples of the alkyl group include methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, s-butyl group, isobutyl group, t-butyl group, n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group, n-nonyl group, n-decyl group, n-undecyl group, n-dodecyl group, n-tridecyl group, n-tetradecyl group, n-pentadecyl group, n-hexadecyl group, n-heptadecyl group, n-octadecyl group, neopentyl group, 1-methylpentyl group, 2-methylpentyl group, 1-pentylhexyl group, 1-butylpentyl group, 1-heptyloctyl group, and 3-methylpentyl group. Additionally, the alkyl group may be optionally substituted. The carbons in the alkyl chain can be replaced by other hetero atoms. Of the above, preferred are methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, s-butyl group, isobutyl group, t-butyl group, n-pentyl group, and neopentyl group.

Cycloalkyl—as used herein contemplates cyclic alkyl groups. Preferred cycloalkyl groups are those containing 4 to 10 ring carbon atoms and includes cyclobutyl, cyclopentyl, cyclohexyl, 4-methylcyclohexyl, 4,4-dimethylcylcohexyl, 1-adamantyl, 2-adamantyl, 1-norbornyl, 2-norbornyl and the like. Additionally, the cycloalkyl group may be optionally substituted. The carbons in the ring can be replaced by other hetero atoms.

Alkenyl—as used herein contemplates both straight and branched chain alkene groups.

Preferred alkenyl groups are those containing 2 to 15 carbon atoms. Examples of the alkenyl group include vinyl group, allyl group, 1-butenyl group, 2-butenyl group, 3-butenyl group, 1,3-butandienyl group, 1-methylvinyl group, styryl group, 2,2-diphenylvinyl group, 1,2-diphenylvinyl group, 1-methylallyl group, 1,1-dimethylallyl group, 2-methylallyl group, 1-phenylallyl group, 2-phenylallyl group, 3-phenylallyl group, 3,3-diphenylallyl group, 1,2-dimethylallyl group, 1-phenyll-butenyl group, and 3-phenyl-1-butenyl group. Additionally, the alkenyl group may be optionally substituted.

Alkynyl—as used herein contemplates both straight and branched chain alkyne groups. Preferred alkynyl groups are those containing 2 to 15 carbon atoms. Additionally, the alkynyl group may be optionally substituted.

Aryl or aromatic group—as used herein includes noncondensed and condensed systems. Preferred aryl groups are those containing six to sixty carbon atoms, preferably six to twenty carbon atoms, more preferably six to twelve carbon atoms. Examples of the aryl group include phenyl, biphenyl, terphenyl, triphenylene, tetraphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene, preferably phenyl, biphenyl, terphenyl, triphenylene, fluorene, and naphthalene. Additionally, the aryl group may be optionally substituted. Examples of the non-condensed aryl group include phenyl group, biphenyl-2-yl group, biphenyl-3-yl group, biphenyl-4-yl group, p-terphenyl-4-yl group, p-terphenyl-3-yl group, p-terphenyl-2-yl group, m-terphenyl-4-yl group, m-terphenyl-3-yl group, m-terphenyl-2-yl group, o-tolyl group, m-tolyl group, p-tolyl group, p-t-butylphenyl group, p-(2-phenylpropyl)phenyl group, 4′-methylbiphenylyl group, 4″-t-butyl p-terphenyl-4-yl group, o-cumenyl group, m-cumenyl group, p-cumenyl group, 2,3-xylyl group, 3,4-xylyl group, 2,5-xylyl group, mesityl group, and m-quarterphenyl group.

Heterocyclic group or heterocycle—as used herein includes aromatic and non-aromatic cyclic groups. Hetero-aromatic also means heteroaryl. Preferred non-aromatic heterocyclic groups are those containing 3 to 7 ring atoms which include at least one hetero atom such as nitrogen, oxygen, and sulfur. The heterocyclic group can also be an aromatic heterocyclic group having at least one heteroatom selected from nitrogen atom, oxygen atom, sulfur atom, and selenium atom.

Heteroaryl—as used herein includes noncondensed and condensed hetero-aromatic groups that may include from one to five heteroatoms. Preferred heteroaryl groups are those containing three to thirty carbon atoms, preferably three to twenty carbon atoms, more preferably three to twelve carbon atoms. Suitable heteroaryl groups include dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine, preferably dibenzothiophene, dibenzofuran, dibenzoselenophene, carbazole, indolocarbazole, imidazole, pyridine, triazine, benzimidazole, 1,2-azaborine, 1,3-azaborine, 1,4-azaborine, borazine, and aza-analogs thereof. Additionally, the heteroaryl group may be optionally substituted.

Alkoxy—it is represented by —O-Alkyl. Examples and preferred examples thereof are the same as those described above. Examples of the alkoxy group having 1 to 20 carbon atoms, preferably 1 to 6 carbon atoms include methoxy group, ethoxy group, propoxy group, butoxy group, pentyloxy group, and hexyloxy group. The alkoxy group having 3 or more carbon atoms may be linear, cyclic or branched.

Aryloxy—it is represented by —O-Aryl or —O-heteroaryl. Examples and preferred examples thereof are the same as those described above. Examples of the aryloxy group having 6 to 40 carbon atoms include phenoxy group and biphenyloxy group.

Arylalkyl—as used herein contemplates an alkyl group that has an aryl substituent. Additionally, the arylalkyl group may be optionally substituted. Examples of the arylalkyl group include benzyl group, 1-phenylethyl group, 2-phenylethyl group, 1-phenylisopropyl group, 2-phenylisopropyl group, phenyl-t-butyl group, alpha.-naphthylmethyl group, 1-alpha.-naphthylethyl group, 2-alpha-naphthylethyl group, 1-alpha-naphthylisopropyl group, 2-alpha-naphthylisopropyl group, beta-naphthylmethyl group, 1-beta-naphthylethyl group, 2-beta-naphthylethyl group, 1-beta-naphthylisopropyl group, 2-beta-naphthylisopropyl group, p-methylbenzyl group, m-methylbenzyl group, o-methylbenzyl group, p-chlorobenzyl group, m-chlorobenzyl group, o-chlorobenzyl group, p-bromobenzyl group, m-bromobenzyl group, o-bromobenzyl group, p-iodobenzyl group, m-iodobenzyl group, o-iodobenzyl group, p-hydroxybenzyl group, m-hydroxybenzyl group, o-hydroxybenzyl group, p-aminobenzyl group, m-aminobenzyl group, o-aminobenzyl group, p-nitrobenzyl group, m-nitrobenzyl group, o-nitrobenzyl group, p-cyanobenzyl group, m-cyanobenzyl group, o-cyanobenzyl group, 1-hydroxy-2-phenylisopropyl group, and 1-chloro-2-phenylisopropyl group. Of the above, preferred are benzyl group, p-cyanobenzyl group, m-cyanobenzyl group, o-cyanobenzyl group, 1-phenylethyl group, 2-phenylethyl group, 1-phenylisopropyl group, and 2-phenylisopropyl group.

The term “aza” in azadibenzofuran, aza-dibenzothiophene, etc. means that one or more of the C—H groups in the respective aromatic fragment are replaced by a nitrogen atom. For example, azatriphenylene encompasses dibenzo[f,h]quinoxaline, dibenzo[f,h]quinoline and other analogues with two or more nitrogens in the ring system. One of ordinary skill in the art can readily envision other nitrogen analogs of the aza-derivatives described above, and all such analogs are intended to be encompassed by the terms as set forth herein.

The alkyl, cycloalkyl, alkenyl, alkynyl, arylalkyl, heterocyclic group, aryl, and heteroaryl may be unsubstituted or may be substituted with one or more substituents selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, arylalkyl, alkoxy, aryloxy, amino, cyclic amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, an acyl group, a carbonyl group, a carboxylic acid group, an ether group, an ester group, a nitrile group, an isonitrile group, a thioalkyl group, a sulfinyl group, a sulfonyl group, a phosphino group, and combinations thereof.

It is to be understood that when a molecular fragment is described as being a substituent or otherwise attached to another moiety, its name may be written as if it were a fragment (e.g. phenyl, phenylene, naphthyl, dibenzofuryl) or as if it were the whole molecule (e.g. benzene, naphthalene, dibenzofuran). As used herein, these different ways of designating a substituent or attached fragment are considered to be equivalent.

In the compounds mentioned in this disclosure, the hydrogen atoms can be partially or fully replaced by deuterium. Other atoms such as carbon and nitrogen, can also be replaced by their other stable isotopes. The replacement by other stable isotopes in the compounds may be preferred due to its enhancements of device efficiency and stability.

In the compounds mentioned in this disclosure, multiple substitutions refer to a range that includes a double substitution, up to the maximum available substitutions. When a substitution in the compounds mentioned in this disclosure represents multiple substitutions (including di, tri, tetra substitutions etc.), that means the substituent may exist at a plurality of available substitution positions on its linking structure, the substituents present at a plurality of available substitution positions may be the same structure or different structures.

In the compounds mentioned in this disclosure, the expression that adjacent substituents can be optionally joined to form a ring is intended to be taken to mean that two radicals are linked to each other by a chemical bond. This is illustrated by the following scheme:

Furthermore, the expression that adjacent substituents can be optionally joined to form a ring is also intended to be taken to mean that in the case where one of the two radicals represents hydrogen, the second radical is bonded at a position to which the hydrogen atom was bonded, with formation of a ring. This is illustrated by the following scheme:

According to an embodiment of the present disclosure, a metal complex having a L_a ligand is disclosed, wherein L_a comprises a structure represented by Formula 1:

• • wherein, Cy is a substituted or unsubstituted aryl or heteroaryl group having 5 to 24 ring atoms;
  • wherein, Cy is bonded to a metal through a metal-carbon bond or a metal-nitrogen bond;
  • wherein, X₁ to X₄ are each independently selected from C, CR_x1 or N, and at least one of X₁ to X₄ is C and connected to Cy; when more than one of X₁ to X₄ is CR_x1, the R_x1 may be the same or different;
  • wherein, X₅ to X₈ are each independently selected from CR_x2 or N; when more than one of X₅ to X₈ is CR_x2, the R_x2 may be the same or different;
  • X is selected from the group consisting of O, S, Se, NR_x3, CR_x4R_x5 and SiR_x6R_x7; wherein, R_x1, R_x2, R_x3, R_x4, R_x5, R_x6 and R_x7 are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted arylalkyl group having 7-30 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted aryloxy group having 6-30 carbon atoms, a substituted or unsubstituted alkenyl group having 2-20 carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a substituted or unsubstituted arylsilyl group having 6-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof,
  • wherein, at least one of R_x1 and R_x2 is a cyano group;
  • any two adjacent substituents can optionally be joined to form a ring;
  • X₁, X₂, X₃ or X₄ is connected to the metal through a metal-carbon bond or a metal-nitrogen bond.

According to an embodiment of the present disclosure, Cy is any structure selected from the group consisting of:

• • wherein
  • R may represent mono-substitution, up to the maximum available multi-substitution, or no substitution; when more than one R exists in any of the above structures, the R may be the same or different;
  • wherein, R is independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted arylalkyl group having 7-30 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted aryloxy group having 6-30 carbon atoms, a substituted or unsubstituted alkenyl group having 2-20 carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a substituted or unsubstituted arylsilyl group having 6-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;
  • any two adjacent substituents can optionally be joined to form a ring;
  • wherein, “#” represents a position at which the metal is connected, and “*” represents a position at which X₁, X₂, X₃ or X₄ is connected.

According to an embodiment of the present disclosure, the metal complex has a general formula of M(L_a)_m(L_b)_n(L_c)_q, wherein L_a is a first ligand coordinated to the metal M, and L_b and L_c are a second ligand and a third ligand coordinated to the metal M, respectively, wherein L_b and L_c may be the same or different; L_a, L_b and L_c can optionally be linked to form a multidentate ligand;

• • wherein, m is 1, 2 or 3, n is 0, 1 or 2, q is 0, 1 or 2, and m+n+q is equal to the oxidation state of M;
  • wherein, the metal M is selected from the group consisting of Cu, Ag, Au, Ru, Rh, Pd, Os, Ir, and Pt; preferably, wherein, the metal M is selected from Pt, Os or Ir;
  • wherein, L_a is independently selected from the group consisting of:

• • wherein, in the structure of L_a,
  • X is selected from the group consisting of O, S, Se, NR_x3, CR_x4R_x5 and SiR_x6R_x7;
  • R₁, R₂, R₃ and R₄ may represent mono-, di-, tri- or tetra-substitution, or no substitution; R₁, R₂, R₃, R₄, R_x3, R_x4, R_x5, R_x6 and R_x7 are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted arylalkyl group having 7-30 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted aryloxy group having 6-30 carbon atoms, a substituted or unsubstituted alkenyl group having 2-20 carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a substituted or unsubstituted arylsilyl group having 6-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof,
  • wherein, at least one of R₃ and R₄ is a cyano group;
  • any two adjacent substituents can optionally be joined to form a ring;
  • wherein, L_b and L_c are independently selected from the group consisting of:

• • wherein
  • R_a, R_b, and R_c may represent mono-, di-, tri- or tetra-substitution, or no substitution;
  • X_b is selected from the group consisting of: O, S, Se, NR_N1, and CR_C1R_C2;
  • R_a, R_b, R_c, R_N1, R_C1 and R_C2 are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted arylalkyl group having 7-30 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted aryloxy group having 6-30 carbon atoms, a substituted or unsubstituted alkenyl group having 2-20 carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a substituted or unsubstituted arylsilyl group having 6-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;
  • any two adjacent substituents can optionally be joined to form a ring.

According to an embodiment of the present disclosure, in the structural formula of the ligand L_a, X is selected from O, S or Se.

According to an embodiment of the present disclosure, the metal complex has any one of the structures according to Formula 2 to Formula 10:

• • wherein
  • m is 1, 2 or 3;
  • X is selected from 0, S or Se;
  • R₁, R₃, and R₄ may represent mono-, di-, tri- or tetra-substitution, or no substitution;
  • R_a, R_b, and R_c may represent mono-, di-, tri- or tetra-substitution, or no substitution;
  • R₁, R₃, R₄, R_a, R_b and R_c are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted arylalkyl group having 7-30 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted aryloxy group having 6-30 carbon atoms, a substituted or unsubstituted alkenyl group having 2-20 carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a substituted or unsubstituted arylsilyl group having 6-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;
  • wherein, at least one of R₃ and R₄ is a cyano group;
  • any two adjacent substituents can optionally be joined to form a ring.

According to an embodiment of the present disclosure, the metal complex has the structure of Formula 2-a:

• • wherein,
  • m is 1, 2 or 3;
  • X is selected from 0, S or Se;
  • R₃ and R₄ may represent mono-, di-, tri- or tetra-substitution, or no substitution;
  • R_a, R_b, and R_c may represent mono-, di-, tri- or tetra-substitution, or no substitution;
  • wherein, R₁₁, R₁₂, R₁₃, R₁₄, R₃, R₄, R_a, and R_b are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted arylalkyl group having 7-30 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted aryloxy group having 6-30 carbon atoms, a substituted or unsubstituted alkenyl group having 2-20 carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a substituted or unsubstituted arylsilyl group having 6-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof,
  • wherein, at least one of R₃ and R₄ is a cyano group;
  • any two adjacent substituents can optionally be joined to form a ring.

According to an embodiment of the present disclosure, when at least one of R₁₁ and R₁₄ in Formula 2-a is not hydrogen, R₁₂ and R₁₃ are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted arylalkyl group having 7-30 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted aryloxy group having 6-30 carbon atoms, a substituted or unsubstituted alkenyl group having 2-20 carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a substituted or unsubstituted arylsilyl group having 6-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.

According to an embodiment of the present disclosure, when R₁ and R₁₄ in Formula 2-a are both hydrogen, R₁₂ and R₁₃ are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, and the total number of carbon atoms in R₁₂ and R₁₃ is less than or equal to 1.

According to an embodiment of the present disclosure, at least one of X₅ to X₈ in the Formula 1 is CR_x2, and the R_x2 is a cyano group.

According to an embodiment of the present disclosure, X₅ to X₈ in the Formula 1 are each independently selected from CR_x2, and at least one of the R_x2 is a cyano group.

According to an embodiment of the present disclosure, R₄ may represent mono-, di-, tri- or tetra-substitution; when more than one R₄ exists, the R₄ may be the same or different; R₄ is selected from the group consisting of deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a cyano group, and combinations thereof; and at least one R₄ is a cyano group.

According to an embodiment of the present disclosure, the ligand L_a is selected from the group consisting of L_a1 to L_a575. The specific structures of L_a1 to L_a575 are described in claim 8.

According to an embodiment of the present disclosure, the ligand L_a is selected from the group consisting of L_a1 to L_a957. The specific structures of L_a1 to L_a957 are described in claim 8.

According to an embodiment of the present disclosure, the hydrogen in L_a can be partially or fully deuterated.

According to an embodiment of the present disclosure, the hydrogen on the aryl group in L_a can be partially or fully deuterated.

According to an embodiment of the present disclosure, the hydrogen on the alkyl group in L_a can be partially or fully deuterated.

According to an embodiment of the present disclosure, the hydrogen in L_a can be partially or fully deuterated, and the ligand L_a is selected from the group consisting of L_a958 to L_a1019, wherein the specific structures of L_a958 to L_a1019 are described in claim 14.

According to an embodiment of the present disclosure, the metal complex has the Formula IrL_a(L_b)₂ or Ir(L_a)₂L_b, wherein L_a is one or two selected from L_a1 to L_a575, and L_b is one or two selected from the group consisting of L_b1-L_b41, wherein the specific structures of L_b1-L_b41 are described in claim 17.

According to an embodiment of the present disclosure, the metal complex has the Formula IrL_a(L_b)₂ or Ir(L_a)₂L_b, wherein L_a is one or two selected from L_a1 to L_a1019, and L_b is one or two selected from the group consisting of:

According to an embodiment of the present disclosure, the metal complex has the Formula Ir(L_a)₂L_c or IrL_a(L_c)₂, wherein L_a is one or two selected from L_a1 to L_a1019, and L_c is one or two selected from the group consisting of L_c1 to L_c360, wherein the specific structures of L_c1 to L_c360 are described in claim 18.

According to an embodiment of the present disclosure, the metal complex has a structure represented by any one selected from Metal complex 1 to Metal complex 316:

Wherein Metal complex 1 to Metal complex 226 have the structure of IrL_a(L_b)₂, wherein the two L_b are the same, wherein L_a and L_b correspond to the structures as shown in the following table, respectively:

Metal			Metal
complex	La	Lb	complex	La	Lb
1	La1	Lb1	2	La2	Lb1
3	La3	Lb1	4	La4	Lb1
5	La121	Lb1	6	La122	Lb1
7	La123	Lb1	8	La137	Lb1
9	La138	Lb1	10	La139	Lb1
11	La153	Lb1	12	La154	Lb1
13	La155	Lb1	14	La169	Lb1
15	La170	Lb1	16	La171	Lb1
17	La221	Lb1	18	La222	Lb1
19	La293	Lb1	20	La294	Lb1
21	La295	Lb1	22	La297	Lb1
23	La298	Lb1	24	La299	Lb1
25	La313	Lb1	26	La314	Lb1
27	La415	Lb1	28	La416	Lb1
29	La467	Lb1	30	La468	Lb1
31	La487	Lb1	32	La488	Lb1
33	La507	Lb1	34	La508	Lb1
35	La516	Lb1	36	La517	Lb1
37	La527	Lb1	38	La528	Lb1
39	La547	Lb1	40	La548	Lb1
41	La576	Lb1	42	La577	Lb1
43	La592	Lb1	44	La593	Lb1
45	La640	Lb1	46	La652	Lb1
47	La692	Lb1	48	La693	Lb1
49	La704	Lb1	50	La842	Lb1
51	La854	Lb	52	La896	Lb1
53	La962	Lb	54	La966	Lb1
55	La970	Lb	56	La973	Lb1
57	La974	Lb1	58	La975	Lb1
59	La976	Lb1	60	La978	Lb1
61	La985	Lb1	62	La987	Lb1
63	La988	Lb	64	La999	Lb1
65	La1003	Lb1	66	La1010	Lb1
67	Lal	Lb3	68	La2	Lb3
69	La3	Lb3	70	La4	Lb3
71	La121	Lb3	72	La122	Lb3
73	La123	Lb3	74	La137	Lb3
75	La138	Lb3	76	La139	Lb3
77	La293	Lb3	78	La294	Lb3
79	La297	Lb3	80	La298	Lb3
81	La576	Lb3	82	La577	Lb3
83	La592	Lb3	84	La593	Lb3
85	La640	Lb3	86	La652	Lb3
87	La692	Lb3	88	La693	Lb3
89	La704	Lb3	90	La842	Lb3
91	La854	Lb3	92	La896	Lb3
93	La962	Lb3	94	La966	Lb3
95	La970	Lb3	96	La973	Lb3
97	La974	Lb3	98	La975	Lb3
99	La976	Lb3	100	La978	Lb3
101	La985	Lb3	102	La987	Lb3
103	La988	Lb3	104	La999	Lb3
105	La1003	Lb3	106	La1010	Lb3
107	Lal	Lb4	108	La2	Lb4
109	La3	Lb4	110	La4	Lb4
111	La121	Lb4	112	La122	Lb4
113	La123	Lb4	114	La137	Lb4
115	La138	Lb4	116	La139	Lb4
117	La293	Lb4	118	La294	Lb4
119	La297	Lb4	120	La298	Lb4
121	La576	Lb4	122	La577	Lb4
123	La592	Lb4	124	La593	Lb4
125	La640	Lb4	126	La652	Lb4
127	La692	Lb4	128	La693	Lb4
129	La704	Lb4	130	La842	Lb4
131	La854	Lb4	132	La896	Lb4
133	La962	Lb4	134	La966	Lb4
135	La970	Lb4	136	La973	Lb4
137	La974	Lb4	138	La975	Lb4
139	La976	Lb4	140	La978	Lb4
141	La985	Lb4	142	La987	Lb4
143	La988	Lb4	144	La999	Lb4
145	La1003	Lb4	146	La1010	Lb4
147	La1	Lb8	148	La2	Lb8
149	La3	Lb8	150	La4	Lb8
151	La121	Lb8	152	La122	Lb8
153	La123	Lb8	154	La137	Lb8
155	La138	Lb8	156	La139	Lb8
157	La293	Lb8	158	La294	Lb8
159	La297	Lb8	160	La298	Lb8
161	La576	Lb8	162	La577	Lb8
163	La592	Lb8	16	La593	Lb8
165	La640	Lb8	166	La652	Lb8
167	La692	Lb8	168	La693	Lb8
169	La704	Lb8	170	La842	Lb8
171	La854	Lb8	172	La896	Lb8
173	La962	Lb8	174	La966	Lb8
175	La970	Lb8	176	La973	Lb8
177	La974	Lb8	178	La975	Lb8
179	La976	Lb8	180	La978	Lb8
181	La985	Lb8	182	La987	Lb8
183	La988	Lb8	184	La999	Lb8
185	La1003	Lb8	186	La1010	Lb8
187	La1	Lb30	188	La2	Lb30
189	La3	Lb30	190	La4	Lb30
191	La121	Lb30	192	La122	Lb30
193	La123	Lb30	194	La137	Lb30
195	La138	Lb30	196	La139	Lb30
197	La293	Lb30	198	La294	Lb30
199	La297	Lb30	200	La298	Lb30
201	La576	Lb30	202	La577	Lb30
203	La592	Lb30	204	La593	Lb30
205	La640	Lb30	206	La652	Lb30
207	La692	Lb30	208	La693	Lb30
209	La704	Lb30	210	La842	Lb30
211	La854	Lb30	212	La896	Lb30
213	La962	Lb30	214	La966	Lb30
215	La970	Lb30	216	La973	Lb30
217	La974	Lb30	218	La975	Lb30
219	La976	Lb30	220	La978	Lb30
221	La985	Lb30	222	La987	Lb30
223	La988	Lb30	224	La999	Lb30
225	La1003	Lb30	226	La1010	Lb30

Wherein Metal complex 227 to Metal complex 274 have the structure of Ir(L_a)₂L_c, wherein the two L_a are the same, wherein L_a and L_c correspond to the structures as shown in the following table, respectively:

Metal			Metal
complex	La	Lc	complex	La	Lc
227	La323	Lc1	228	La324	Lc1
229	La328	Lc1	230	La329	Lc1
231	La333	Lc1	232	La334	Lc1
233	La338	Lc1	234	La339	Lc1
235	La343	Lc1	236	La344	Lc1
237	La348	Lc1	238	La349	Lc1
239	La353	Lc1	240	La354	Lc1
241	La358	Lc1	242	La359	Lc1
243	La363	Lc1	244	La364	Lc1
245	La368	Lc1	246	La369	Lc1
247	La373	Lc1	248	La374	Lc1
249	La388	Lc1	250	La389	Lc1
251	La323	L31	252	La324	L31
253	La328	L31	254	La329	L31
255	La333	L31	256	La334	L31
257	La338	L31	258	La339	L31
259	La343	L31	260	La344	L31
261	La348	L31	262	La349	L31
263	La353	L31	264	La354	L31
265	La358	L31	266	La359	L31
267	La363	L31	268	La364	L31
269	La368	L31	270	La369	L31
271	La373	L31	272	La374	L31
273	La388	L31	274	La389	L31

Wherein Metal complex 275 to Metal complex 316 have the structure of Ir(L_a)₃, wherein the three L_a are the same, wherein L_a corresponds to the structures as shown in the following table:

Metal
complex La
275     La1
276     La2
277     La3
278     La121
279     La122
280     La137
281     La138
282     La293
283     La297
284     La298
285     La487
286     La488
287     La507
288     La508
289     La547
290     La548
291     La576
292     La577
293     La640
294     La641
295     La652
296     La653
297     La692
298     La693
299     La704
300     La842
301     La854
302     La896
303     La962
304     La966
305     La970
306     La973
307     La974
308     La975
309     La976
310     La978
311     La985
312     La987
313     La988
314     La999
315     La1003
316     La1010

According to an embodiment of the present disclosure, a compound selected from the group consisting of Compound 1 to Compound 136 is also disclosed. Wherein, the specific structures of Compound 1 to Compound 136 are described in claim 14.

According to an embodiment of the present disclosure, an electroluminescent device is also disclosed, which includes:

• • an anode,
  • a cathode, and
  • an organic layer disposed between the anode and the cathode, wherein the organic layer comprises a metal complex comprising the ligand L_a represented by Formula 1:

• • wherein, Cy is a substituted or unsubstituted aryl or heteroaryl group having 5 to 24 ring atoms;
  • the Cy is bonded to a metal through a metal-carbon bond or a metal-nitrogen bond;
  • X₁ to X₄ are each independently selected from C, CR_x1 or N, and at least one of X₁ to X₄ is C which is connected to the Cy; when more than one of X₁ to X₄ is CR_x1, the R_x1 may be the same or different;
  • X₅ to X₈ are each independently selected from CR_x2 or N; when more than one of X₅ to X₈ is CR_x2, the R_x2 may be the same or different;
  • X is selected from the group consisting of O, S, Se, NR_x3, CR_x4R_x5 and SiR_x6R_x7;
  • R_x1, R_x2, R_x3, R_x4, R_x5, R_x6 and R_x7 are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted arylalkyl group having 7-30 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted aryloxy group having 6-30 carbon atoms, a substituted or unsubstituted alkenyl group having 2-20 carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a substituted or unsubstituted arylsilyl group having 6-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof,
  • wherein, at least one of R_x1 and R_x2 is a cyano group;
  • any two adjacent substituents can optionally be joined to form a ring;
  • X₁, X₂, X₃ or X₄ are connected to the metal through a metal-carbon bond or a metal-nitrogen bond.

According to an embodiment of the present disclosure, in the electroluminescent device, the organic layer is a light-emitting layer, and the metal complex is a light-emitting material.

According to an embodiment of the present disclosure, in the electroluminescent device, the organic layer further includes a host material.

According to an embodiment of the present disclosure, in the electroluminescent device, the organic layer further includes at least two host materials.

According to an embodiment of the present disclosure, the host material comprises at least one chemical group selected from the group consisting of benzene, biphenyl, pyridine, pyrimidine, triazine, carbazole, azacarbazole, indolocarbazole, dibenzothiophene, azadibenzothiophen, dibenzofuran, azadibenzofuran, dibenzoselenophene, azadibenzoselenophene, triphenylene, azatriphenylene, fluorene, silicon-fluorene, naphthalene, quinoline, isoquinoline, quinazoline, quinoxaline, phenanthrene, azaphenanthrene, and combinations thereof.

According to an embodiment of the present disclosure, the electroluminescent device is incorporated into a device selected from the group consisting of a consumption product, an electronic component module, an organic light-emitting device and a lighting panel.

According to another embodiment of the present disclosure, a compound formulation is also disclosed, which comprises a metal complex. The specific structure of the metal complex is shown in any one of the foregoing embodiments.

Combination with Other Materials

The materials described in the present disclosure for a particular layer in an organic light emitting device can be used in combination with various other materials present in the device. The combinations of these materials are described in more detail in U.S. Pat. App. No. 20160359122 at paragraphs 0132-0161, which is incorporated by reference herein in its entirety. The materials described or referred to the disclosure are non-limiting examples of materials that may be useful in combination with the compounds disclosed herein, and one of skill in the art can readily consult the literature to identify other materials that may be useful in combination.

The materials described herein as useful for a particular layer in an organic light emitting device may be used in combination with a variety of other materials present in the device. For example, dopants disclosed herein may be used in combination with a wide variety of hosts, transport layers, blocking layers, injection layers, electrodes and other layers that may be present. The combination of these materials is described in detail in paragraphs 0080-0101 of U.S. Pat. App. No. 20150349273, which is incorporated by reference herein in its entirety. The materials described or referred to the disclosure are non-limiting examples of materials that may be useful in combination with the compounds disclosed herein, and one of skill in the art can readily consult the literature to identify other materials that may be useful in combination.

In the embodiments of material synthesis, all reactions were performed under nitrogen protection unless otherwise stated. All reaction solvents were anhydrous and used as received from commercial sources. Synthetic products were structurally confirmed and tested for properties using one or more conventional equipment in the art (including, but not limited to, nuclear magnetic resonance instrument produced by BRUKER, liquid chromatograph produced by SHIMADZU, liquid chromatograph-mass spectrometry produced by SHIMADZU, gas chromatograph-mass spectrometry produced by SHIMADZU, differential Scanning calorimeters produced by SHIMADZU, fluorescence spectrophotometer produced by SHANGHAI LENGGUANG TECH., electrochemical workstation produced by WUHAN CORRTEST, and sublimation apparatus produced by ANHUI BEQ, etc.) by methods well known to the persons skilled in the art. In the embodiments of the device, the characteristics of the device were also tested using conventional equipment in the art (including, but not limited to, evaporator produced by ANGSTROM ENGINEERING, optical testing system produced by SUZHOU FATAR, life testing system produced by SUZHOU FATAR, and ellipsometer produced by BEIJING ELLITOP, etc.) by methods well known to the persons skilled in the art. As the persons skilled in the art are aware of the above-mentioned equipment use, test methods and other related contents, the inherent data of the sample can be obtained with certainty and without influence, so the above related contents are not further described in this patent.

Synthesis Examples of the Materials:

The method for preparing the compound of the present disclosure is not limited, and the following compounds are exemplified as typical but non-limiting examples. The synthetic route and preparation method of which are as follows:

Synthesis Example 1: Synthesis of Compound IrL_a1(L_b1)₂ (Metal Complex 1)

Step 1:

To a dried 1000 mL round bottom flask, 3-chloro-2-methoxyphenylboronic acid (20.00 g, 107.29 mmol), 2-fluoro-3-bromobenzonitrile (20.43 g, 102.20 mmol), tetrakis(triphenylphosphine)palladium (Pd(PPh₃)₄) (4.39 g, 3.74 mmol), potassium carbonate (32.48 g, 235.40 mmol), 1,4-dioxane (500 mL) and water (100 mL) were sequentially added. The reaction system was then replaced with N₂ three times and protected by N₂, then it was heated in a heating mantle and stirred under reflux for 12 h. After the reaction was cooled, it was extracted with ethyl acetate, washed with saturated brine three times, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The crude product was purified by column chromatography, eluting with 5% (v/v) ethyl acetate (EA)/petroleum ether (PE), to give 22 g of white product intermediate 1 (74.8% yield).

Step 2:

In a dried 500 mL three-necked flask, intermediate 1 (22.00 g, 84.30 mmol) and dichloromethane (350 mL) were added. The reaction system was then replaced with N₂ three times and protected by N₂, and then stirred in an ice bath at 0° C. for 5 minutes. Boron tribromide was added dropwise thereto. After the completion of the addition, the reaction was warmed up to room temperature and stirred for 12 h. After the reaction was completed, the reaction was quenched with ice-water in an ice bath and neutralized with a saturated aqueous solution of sodium bicarbonate. A large amount of white solid product was precipitated, which was directly filtered, washed with water three times, and dried under reduced pressure to obtain 19.7 g of white solid product intermediate 2 (94.4% yield).

Step 3:

In a dried 500 mL round-bottomed flask, intermediate 2 (19.7 g, 79.6 mmol), potassium carbonate (32.9 g, 238.8 mmol) and DMF (300 mL) were added successively, and then the reaction was heated in a heating mantle at 100° C. and stirred for 12 h. After the reaction was completed, it was cooled and filtered through celite. The organic phase was washed with saturated brine, extracted twice with ethyl acetate, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The crude product was purified by column chromatography, eluting with a 20% (v/v) dichloromethane/petroleum ether solution to give 11 g of intermediate 3 as a white solid (60.7% yield).

Step 4:

In a dried 500 mL round bottom flask, intermediate 3 (9.60 g, 42.19 mmol), bis(pinacolato)diboron (13.93 g, 54.86 mmol), X-Phos (0.99 g, 2.10 mmol), palladium acetate (0.47 g, 2.10 mmol), potassium acetate (10.30 g, 105.00 mmol) and dioxane (200 mL) were added successively. The reaction system was then replaced with N₂ three times and protected by N₂, heated at 100° C. and stirred overnight. After the reaction was completed, it was filtered through celite and anhydrous magnesium sulfate, and washed twice with ethyl acetate. The organic phase was collected and concentrated under reduced pressure to obtain a crude product, which was directly used in the next step.

Step 5:

In a dried 500 mL round bottom flask, intermediate 4 (crude product), 2-bromopyridine (6.23 g, 39.45 mmol), Pd(PPh₃)₄(2.07 g, 1.79 mmol), sodium carbonate (9.49 g, 89.50 mmol), dioxane (250 mL) and water (50 mL) were added successively. The reaction system was then replaced with N₂ three times and protected by N₂, heated at 100° C. and reacted for 12 h. After the reaction was completed, it was extracted with ethyl acetate, washed with saturated brine three times, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The crude product was purified by column chromatography by eluting with a gradient of PE:EA=10: 1 to 5:1 (v/v) to obtain 11.4 g of intermediate 5 as a white solid (98% yield). Intermediate 5 is Compound 1 corresponding to ligand L_a, and the structure of the product was confirmed by NMR and GCMS.

Step 6:

In a dried 500 mL round bottom flask, intermediate 5 (3.52 g, 12.96 mmol), iridium complex (4.50 g, 6.31 mmol), and ethanol (250 mL) were added successively. The reaction system was then replaced with N₂ three times and protected by N₂, and then heated to reflux for 24 h.

After the reaction was cooled, it was filtered through celite. The mixture was washed twice with methanol and n-hexane. The yellow solid above the celite was dissolved in dichloromethane. The organic phase was collected, concentrated under reduced pressure, and purified by column chromatography to obtain the compound IrL_a1(L_b1)₂ (Metal complex 1) as a yellow solid (1.5 g, 28.7% yield). The product was identified as the target product with a molecular weight of 770.

Synthesis Example 2: Synthesis of Compound IrL_a4(L_b1)₂ (Metal Complex 4)

Step 1:

In a dried 500 mL round bottom flask, 6-chloro-dibenzofuran-1-nitrile (4.6 g, 20.2 mmol), bis(pinacolato)diboron (5.9 g, 23.2 mmol), palladium acetate (0.14 g, 0.6 mmol), potassium acetate (2.97 g, 30.3 mmol), X-Phos (0.58 g, 1.21 mmol) and 1,4-dioxane (90 mL) were added successively. The reaction system was then replaced with N₂ three times and protected by N₂, heated to reflux and stirred overnight. After the reaction was completed, it was filtered through celite and anhydrous magnesium sulfate, and washed twice with ethyl acetate. The organic phase was collected and concentrated under reduced pressure to obtain intermediate 6, which was directly used in the next step.

Step 2:

In a dried 500 mL round bottom flask, intermediate 6 (6.4 g, 20.2 mmol), 2-bromopyridine (3.2 g, 20.2 mmol), Pd(PPh₃)₄(1.4 g, 1.2 mmol), potassium carbonate (4.2 g, 30.3 mmol), 1,4-dioxane (90 mL) and water (30 mL) were added successively. The reaction system was then replaced with N₂ three times and protected by N₂, heated at 100° C. and reacted for 12 h. After the reaction was completed, it was extracted with ethyl acetate, washed with saturated brine three times, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The crude product was purified by column chromatography by eluting with a gradient of PE:EA=20: 1 to 10:1 (v/v) to obtain 4 g of intermediate 7 as a white solid (74% yield). Intermediate 7 is compound 4 corresponding to ligand L_a, and the structure of the product was confirmed by NMR and GCMS.

Step 3:

In a dried 500 mL round bottom flask, intermediate 7 (2.9 g, 11.0 mmol), iridium complex (4.0 g, 5.5 mmol), and ethanol (250 mL) were added successively. The reaction system was then replaced with N₂ three times and protected by N₂, and then heated to reflux for 24 h.

After the reaction was cooled, it was filtered through celite. The mixture was washed twice with methanol and n-hexane. The yellow solid above the celite was dissolved in dichloromethane. The organic phase was collected, concentrated under reduced pressure, and purified by column chromatography to obtain the compound IrL_a4(L_b1)₂ (Metal complex 4) as a yellow solid (1.5 g, 36% yield). The product structure was identified as the target product with a molecular weight of 770.

Synthesis Example 3: Synthesis of Compound IrL_a2(L_b1)₂ (Metal Complex 2)

Step 1:

To a dried 1000 mL round bottom flask, 3-chloro-2-methoxyphenylboronic acid (12.00 g, 64.37 mmol), 2-fluoro-3-bromobenzonitrile (12.26 g, 61.31 mmol), tetrakis(triphenylphosphine)palladium (Pd(PPh₃)₄) (3.25 g, 3.05 mmol), potassium carbonate (18.61 g, 134.80 mmol), 1,4-dioxane (500 mL) and water (100 mL) were added successively. The reaction system was then replaced with N₂ three times and protected by N₂, then it was heated in a heating mantle and stirred under reflux for 12 h. After the reaction was cooled, it was extracted with ethyl acetate, washed with saturated brine three times, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The crude product was purified by column chromatography, eluting with 5% (v/v) ethyl acetate (EA)/petroleum ether (PE), to give 13.2 g of intermediate 8 as a white product (82.5% yield).

Step 2:

In a dried 500 mL three-necked flask, intermediate 8 (13.20 g, 50.50 mmol), and 350 mL of dichloromethane were added successively. The reaction system was then replaced with N₂ three times and protected by N₂, and stirred in an ice bath at 0° C. for 5 minutes. Boron tribromide (19.0 g, 75.74 mmol) was added dropwise slowly. After the completion of the addition, the reaction was warmed up to room temperature and stirred for 12 h. After the reaction was completed, the reaction was quenched with ice-water in an ice bath and neutralized with a saturated aqueous solution of sodium bicarbonate. A large amount of white solid product was precipitated, which was directly filtered, washed with water three times, and dried under reduced pressure to obtain 11.75 g of intermediate 9 as a white solid (94% yield).

Step 3:

In a dried 500 mL round-bottomed flask, intermediate 9 (11.75 g, 47.47 mmol), potassium carbonate (19.6 g, 142.4 mmol), and DMF (300 mL) were added successively. The mixture was then heated in a heating mantle at 100° C. and stirred for 12 h. After the reaction was completed, it was cooled and filtered through celite. The organic phase was washed with saturated brine, extracted twice with ethyl acetate, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The crude product was purified by column chromatography, eluting with a 20% (v/v) dichloromethane (DCM/petroleum ether(PE)) to give 7.09 g of intermediate 10 as a white solid (65.7% yield).

Step 4:

In a dried 500 mL round bottom flask, intermediate 10 (4.10 g, 18.02 mmol), bis(pinacolato)diboron (5.95 g, 23.42 mmol), X-Phos (0.43 g, 0.90 mmol), palladium acetate (0.20 g, 0.90 mmol), potassium acetate (4.46 g, 45.00 mmol) and dioxane (100 mL) were added successively. The reaction system was then replaced with N₂ three times and protected by N₂, heated at 100° C. and stirred overnight. After the reaction was completed, it was filtered through celite and anhydrous magnesium sulfate, and washed twice with ethyl acetate. The organic phase was collected and concentrated under reduced pressure to obtain crude product intermediate 11, which was directly used in the next step.

Step 5:

In a dried 500 mL round bottom flask, intermediate 11 (crude product), 2-bromopyridine (2.66 g, 16.85 mmol), Pd(PPh₃)₄(0.88 g, 0.76 mmol), sodium carbonate (4.05 g, 38.25 mmol), dioxane (150 mL) and water (30 mL) were added successively. The reaction system was then replaced with N₂ three times and protected by N₂, heated at 100° C. and reacted for 12 h. After the reaction was completed, it was extracted with ethyl acetate, washed with saturated brine three times, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The crude product was purified by column chromatography by eluting with a gradient of PE:EA=10: 1 to 5:1 (v/v) to obtain 4.1 g of intermediate 12 as a white solid (90% yield). Intermediate 12 is compound 2 corresponding to ligand L_a, and the structure of the product was confirmed by NMR and GCMS.

Step 6:

In a dried 500 mL round bottom flask, intermediate 12 (3.52 g, 12.96 mmol), iridium complex (4.50 g, 6.31 mmol), and ethanol (250 mL) were added successively. The reaction system was then replaced with N₂ three times and protected by N₂, and then the reaction was heated to reflux for 24 h. After the reaction was cooled, it was filtered through celite. The mixture was washed twice with methanol and n-hexane. The yellow solid above the celite was dissolved in dichloromethane. The organic phase was collected, concentrated under reduced pressure, and purified by column chromatography to obtain the IrL_a2(L_b1)₂ (Metal complex 2) as a yellow solid (1.3 g, 24.5% yield). The product structure was identified as the target product with a molecular weight of 770.

Synthesis Example 4: Synthesis of Compound IrL_a3(L_b1)₂ (Metal Complex 3)

Step 1:

In a dried 500 mL round bottom flask, 6-chloro-dibenzofuran-2-nitrile (5 g, 22.0 mmol), bis(pinacolato)diboron (6.4 g, 25.3 mmol), X-Phos (0.6 g, 1.3 mmol), palladium acetate (0.15 g, 0.6 mmol), potassium acetate (3.2 g, 32.6 mmol) and dioxane (90 mL) were added successively. The reaction system was then replaced with N₂ three times and heated to reflux and stirred overnight under N₂ protection. After the reaction was completed, it was filtered through celite and anhydrous magnesium sulfate, and washed twice with ethyl acetate. The organic phase was collected and concentrated under reduced pressure to obtain intermediate 13, which was directly used in the next step.

Step 2:

In a dried 500 mL round bottom flask, intermediate 13 (crude product), 2-bromopyridine (3.5 g, 22.2 mmol), Pd(dppf)Cl₂ (0.48 g, 0.66 mmol), potassium carbonate (3.5 g, 25.3 mmol), dioxane (90 mL) and water (30 mL) were added successively. Under N₂ protection, the reaction was heated to reflux and reacted for 12 h. After the reaction was completed, it was extracted with ethyl acetate, washed with saturated brine three times, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The crude product was purified by column chromatography to obtain 3.9 g of intermediate 14 as a white solid (65.6% yield), and the structure of the product was confirmed by NMR and GCMS.

Step 3:

In a dried 250 mL round bottom flask, intermediate 14 (3.5 g, 12.9 mmol), iridium complex (4.6 g, 6.3 mmol), 2-ethoxyethanol (50 mL) and DMF (50 mL) were added successively. Under N₂ protection, the mixture was heated to 85° C. and reacted for 96 h. After the reaction was cooled, it was filtered through celite. The mixture was washed twice with methanol and n-hexane. The yellow solid above the celite was dissolved in dichloromethane. The organic phase was collected, concentrated under reduced pressure, and purified by column chromatography to obtain the compound IrL_a3(L_b1)₂ (Metal complex 3) as a yellow solid (2.1 g, 43.3% yield). The product was identified as the target product with a molecular weight of 770.

Synthesis Example 5: Synthesis of Compound IrL_a1(L_b3)₂ (Metal Complex 67)

Step 1:

In a dried 500 mL round bottom flask, intermediate 5 (2.4 g, 8.9 mmol), iridium complex (3.3 g, 4.4 mmol), and ethanol (250 mL) were added successively. The reaction system was then replaced with N₂ three times and protected by N₂, and then the reaction was heated to reflux for 24 h. After the reaction was cooled, it was filtered through celite. The mixture was washed twice with methanol and n-hexane. The yellow solid above the celite was dissolved in dichloromethane. The organic phase was collected, concentrated under reduced pressure, and purified by column chromatography to obtain the compound IrL_a1(L_b3)₂ (Metal complex 67) as a yellow solid (2.2 g, 63.7% yield). The product was identified as the target product with a molecular weight of 798.

Synthesis Example 6: Synthesis of Compound IrL_a1(L_b4)₂ (Metal Complex 107)

Step 1:

In a dried 500 mL round bottom flask, intermediate 5 (2.2 g, 8.1 mmol), iridium complex (4.0 g, 5.4 mmol), and ethanol (120 mL) were added successively. The reaction system was then replaced with N₂ three times and protected by N₂, and then the reaction was heated to reflux for 24 h. After the reaction was cooled, it was filtered through celite. The mixture was washed twice with methanol and n-hexane. The yellow solid above the celite was dissolved in dichloromethane.

The organic phase was collected, concentrated under reduced pressure, and purified by column chromatography to obtain the compound IrL_a1(L_b4)₂ (Metal complex 107) as a yellow solid (0.8 g, 18.6% yield). The product was identified as the target product with a molecular weight of 798.

Synthesis Example 7: Synthesis of Compound IrL_a1(L_b8)₂ (Metal Complex 147)

Step 1:

In a dried 500 mL round bottom flask, intermediate 5 (2.4 g, 8.9 mmol), iridium complex (3.3 g, 4.4 mmol), and ethanol (250 mL) were added successively. The reaction system was then replaced with N₂ three times and protected by N₂, and then the reaction was heated to reflux for 24 h. After the reaction was cooled, it was filtered through celite. The mixture was washed twice with methanol and n-hexane. The yellow solid above the celite was dissolved in dichloromethane. The organic phase was collected, concentrated under reduced pressure, and purified by column chromatography to obtain the compound IrL_a1(L_b8)₂ (Metal complex 147) as a yellow solid (1.0 g, 27.5% yield). The product was identified as the target product with a molecular weight of 826.

Synthesis Example 8: Synthesis of Compound IrL_a221(L_b1)₂ (Metal Complex 17)

Step 1:

In a dried 500 mL round bottom flask, intermediate 4 (7.0 g, 22.0 mmol), 4-methyl-2-bromopyridine (4.2 g, 24.4 mmol), Pd(dppf)Cl₂ (0.67 g, 0.9 mmol), potassium carbonate (6.4 g, 46.3 mmol), dioxane (90 mL) and water (30 mL) were added successively. Under N₂ protection, the reaction was heated to reflux and reacted for 12 h. After the reaction was completed, it was extracted with ethyl acetate, washed with saturated brine three times, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The crude product was purified by column chromatography to obtain 3 g of intermediate 15 as a white solid (48.0% yield), and the structure of the product was confirmed by NMR and LCMS.

Step 2:

In a dried 250 mL round bottom flask, intermediate 15 (3 g, 10.5 mmol), iridium complex (3.5 g, 5 mmol), and ethanol (100 mL) were added successively. Under N₂ protection, the mixture was heated to reflux and reacted for 36 h. After the reaction was cooled, it was filtered through celite. The mixture was washed twice with methanol and n-hexane. The yellow solid above the celite was dissolved in dichloromethane. The organic phase was collected, concentrated under reduced pressure, and purified by column chromatography to obtain the compound IrL_a221(L_b1)₂ (Metal complex 17) as a yellow solid (1.4 g, 33.6% yield). The product was identified as the target product with a molecular weight of 784.

Synthesis Example 9: Synthesis of Compound IrL_a962(L_b1)₂ (Metal Complex 53)

Step 1:

In a dried 250 mL round bottom flask, intermediate 16 (2.6 g, 9 mmol), iridium complex (3.6 g, 5 mmol), 2-ethoxyethanol (50 mL) and DMF (50 mL) were added successively. Under N₂ protection, the mixture was heated to 85° C. and reacted for 96 h. After the reaction was cooled, it was filtered through celite. The mixture was washed twice with methanol and n-hexane. The yellow solid above the celite was dissolved in dichloromethane. The organic phase was collected, concentrated under reduced pressure, and purified by column chromatography to obtain the compound IrL_a962(L_b1)₂ (Metal complex 53) as a yellow solid (1.3 g, 33.3% yield). The product was identified as the target product with a molecular weight of 787.

Synthesis Example 10: Synthesis of Compound IrL_a962(L_b3)₂ (Metal Complex 93)

Step 1:

In a dried 250 mL round bottom flask, intermediate 16 (2.8 g, 9.7 mmol), iridium complex (4.0 g, 5.4 mmol), 2-ethoxyethanol (50 mL) and DMF (50 mL) were added successively. Under N₂ protection, the mixture was heated to 85° C. and reacted for 96 h. After the reaction was cooled, it was filtered through celite. The mixture was washed twice with methanol and n-hexane. The yellow solid above the celite was dissolved in dichloromethane. The organic phase was collected, concentrated under reduced pressure, and purified by column chromatography to obtain the compound IrL_a962(L_b3)₂ (Metal complex 93) as a yellow solid (0.85 g, 19.3% yield). The product was identified as the target product with a molecular weight of 815.

Synthesis Example 11: Synthesis of Compound IrL_a293(L_b1)₂ (Metal Complex 19)

Step 1:

In a dried 250 mL round bottom flask, intermediate 17 (2.6 g, 7.5 mmol), iridium complex (2.2 g, 6.0 mmol), and ethanol (150 mL) were added successively. Under N₂ protection, the mixture was heated to reflux and reacted for 24 h. After the reaction was cooled, it was filtered through celite. The mixture was washed twice with methanol and n-hexane. The yellow solid above the celite was dissolved in dichloromethane. The organic phase was collected, concentrated under reduced pressure, and purified by column chromatography to obtain the compound IrL_a293(L_b1)₂ (Metal complex 19) as a yellow solid (0.6 g, 12% yield). The product was identified as the target product with a molecular weight of 846.

Synthesis Example 12: Synthesis of Compound IrL_a293(L_b3)₂ (Metal Complex 77)

Step 1:

In a dried 250 mL round bottom flask, intermediate 17 (2.6 g, 7.5 mmol), iridium complex (2.2 g, 6.0 mmol), and ethanol (150 mL) were added successively. Under N₂ protection, the mixture was heated to reflux and reacted for 24 h. After the reaction was cooled, it was filtered through celite. The mixture was washed twice with methanol and n-hexane. The yellow solid above the celite was dissolved in dichloromethane. The organic phase was collected, concentrated under reduced pressure, and purified by column chromatography to obtain the compound IrL_a293(L_b3)₂ (Metal complex 77) as a yellow solid (0.6 g, 12% yield). The product was identified as the target product with a molecular weight of 874.

Synthesis Example 13: Synthesis of Compound IrL_a987(L_b3)₂ (Metal Complex 102)

Step 1:

In a dried 250 mL round bottom flask, intermediate 18 (3.0 g, 8.5 mmol), iridium complex (4.2 g, 5.7 mmol), 2-ethoxyethanol (100 mL) and DMF (100 mL) were added successively. Under N₂ protection, the mixture was heated to 85° C. and reacted for 96 h. After the reaction was cooled, it was filtered through celite. The mixture was washed twice with methanol and n-hexane. The yellow solid above the celite was dissolved in dichloromethane. The organic phase was collected, concentrated under reduced pressure, and purified by column chromatography to obtain the compound IrL_a987(L_b3)₂ (Metal complex 102) as a yellow solid (0.9 g, 18.0% yield). The product was identified as the target product with a molecular weight of 879.

Those skilled in the art should know that the above preparation method is only an exemplary example, and those skilled in the art can obtain other compound structures of the present disclosure by improving it.

DEVICE EXAMPLE

Example 1

Firstly, a glass substrate with a 120 nm-thick indium tin oxide (ITO) anode was cleaned, and then treated with oxygen plasma and UV ozone. After processing, the substrate was oven-dried in a glovebox to remove moisture. The substrate was then mounted on a substrate holder and loaded into a vacuum chamber. The organic layers specified below were deposited by thermal vacuum evaporation sequentially on the ITO anode at a rate of 0.2-2 angstroms per second under a vacuum degree of about 10⁻⁸ Torr. Compound H1 (100 Å) was used as a hole injection layer (HIL). Compound HT (350 Å) was used as a hole transporting layer (HTL). Compound H1 (50 Å) was used as an electron blocking layer (EBL). Then, the compound IrL_a1(L_b1)₂ (Metal complex 1) of the present disclosure was doped in the host compounds H1 and H2 and used as a light-emitting layer (EML, 8:46:46, 400 Å). Compound H2 (100 Å) was used as a hole blocking layer (HBL). On the HBL, a mixture of Compound ET and 8-hydroxyquinolinolato-lithium (Liq) was deposited as an electron transporting layer (ETL, 40:60, 350 Å). Finally, 10 Å of Liq was deposited as an electron injection layer, and 1200 Å of Al was deposited as a cathode. The device was then transferred back to the glovebox and encapsulated with a glass lid and a moisture getter to complete the device.

Example 2

The implementation of Example 2 was the same as that of Example 1, except that the compound IrL_a2(L_b1)₂ (Metal complex 2) of the present disclosure was used in the light-emitting layer instead of the compound IrL_a1(L_b1)₂ (Metal complex 1) of the present disclosure in the Example 1.

Example 3

The implementation of Example 3 was the same as that of Example 1, except that the compound IrL_a1(L_b3)₂ (Metal complex 67) of the present disclosure was used in the light-emitting layer instead of the compound IrL_a1(L_b1)₂ (Metal complex 1) of the present disclosure in the Example 1, respectively.

Example 4

The implementation of Example 4 was the same as that of Example 1, except that the compound IrL_a1(L_b4)₂ (Metal complex 107) of the present disclosure was used in the light-emitting layer instead of the compound IrL_a1(L_b1)₂ (Metal complex 1) of the present disclosure in the Example 1, respectively.

Example 5

The implementation of Example 5 was the same as that of Example 1, except that the compound IrL_a1(L_b8)₂ (Metal complex 147) of the present disclosure was used in the light-emitting layer instead of the compound IrL_a1(L_b1)₂ (Metal complex 1) of the present disclosure in the Example 1, respectively.

Example 6

The implementation of Example 6 was the same as that of Example 1, except that the compound IrL_a962(L_b1)₂ (Metal complex 53) of the present disclosure was used in the light-emitting layer instead of the compound IrL_a1(L_b1)₂ (Metal complex 1) of the present disclosure in the Example 1, respectively.

Example 7

The implementation of Example 7 was the same as that of Example 1, except that the compound IrL_a962(L_b3)₂ (Metal complex 93) of the present disclosure was used in the light-emitting layer instead of the compound IrL_a1(L_b1)₂ (Metal complex 1) of the present disclosure in the Example 1, respectively.

Example 8

The implementation of Example 8 was the same as that of Example 1, except that the compound IrL_a293(L_b3)₂ (Metal complex 77) of the present disclosure was used in the light-emitting layer instead of the compound IrL_a1(L_b1)₂ (Metal complex 1) of the present disclosure in the Example 1, respectively.

Example 9

The implementation of Example 9 was the same as that of Example 1, except that the compound IrL_a987(L_b3)₂ (Metal complex 102) of the present disclosure was used in the light-emitting layer instead of the compound IrL_a1(L_b1)₂ (Metal complex 1) of the present disclosure in the Example 1, respectively.

Comparative Example 1

The implementation of Comparative Example 1 was the same as that of Example 1, except that the comparative compound 1 was used in the light-emitting layer instead of the compound IrL_a1(L_b1)₂ (Metal complex 1) of the present disclosure in the Example 1.

For a layer with more than one materials being used, it was obtained by doping different compounds at the recorded weight ratios.

Part detailed device layer structures and thicknesses are shown in Table 1.

Table 1 The device structure of the device examples

TABLE 1
The device structure of the device examples
Device ID	HIL	HTL	EBL	EML	HBL	ETL
Example 1	Compound	Compound	Compound	Compound	Compound	Compound
	HI	HT	H1	H1:Compound	H2	ET:Liq
	(100 Å)	(350 Å)	(50 Å)	H2:IrLa1(Lb1)2 (Metal	(100 Å)	(40:60)
				Complex 1) (46:46:8)		(350 Å)
				(400 Å)
Example 2	Compound	Compound	Compound	Compound	Compound	Compound
	HI	HT	H1	H1:Compound	H2	ET:Liq
	(100 Å)	(350 Å)	(50 Å)	H2:IrLa2(Lb1)2 (Metal	(100 Å)	(40:60)
				Complex 2) (46:46:8)		(350 Å)
				(400 Å)
Example 3	Compound	Compound	Compound	Compound	Compound	Compound
	HI	HT	H1	H1:Compound	H2	ET:Liq
	(100 Å)	(350 Å)	(50 Å)	H2:IrLa1(Lb3)2 (Metal	(100 Å)	(40:60)
				Complex 67) (46:46:8)		(350 Å)
				(400 Å)
Example 4	Compound	Compound	Compound	Compound	Compound	Compound
	HI	HT	H1	H1:Compound	H2	ET:Liq
	(100 Å)	(350 Å)	(50 Å)	H2:IrLa1(Lb4)2 (Metal	(100 Å)	(40:60)
				Complex 107) (46:46:8)		(350 Å)
				(400 Å)
Example 5	Compound	Compound	Compound	Compound	Compound	Compound
	HI	HT	H1	H1:Compound	H2	ET:Liq
	(100 Å)	(350 Å)	(50 Å)	H2:IrLa1(Lb8)2 (Metal	(100 Å)	(40:60)
				Complex 147) (46:46:8)		(350 Å)
				(400 Å)
Example 6	Compound	Compound	Compound	Compound	Compound	Compound
	HI	HT	H1	H1:Compound	H2	ET:Liq
	(100 Å)	(350 Å)	(50 Å)	H2:IrLa962(Lb1)2 (Metal	(100 Å)	(40:60)
				Complex 53) (46:46:8)		(350 Å)
				(400 Å)
Example 7	Compound	Compound	Compound	Compound	Compound	Compound
	HI	HT	H1	H1:Compound	H2	ET:Liq
	(100 Å)	(350 Å)	(50 Å)	H2:IrLa962(Lb3)2 (Metal	(100 Å)	(40:60)
				Complex 93) (46:46:8)		(350 Å)
				(400 Å)
Example 8	Compound	Compound	Compound	Compound	Compound	Compound
	HI	HT	H1	H1:Compound	H2	ET:Liq
	(100 Å)	(350 Å)	(50 Å)	H2:IrLa293(Lb3)2 (Metal	(100 Å)	(40:60)
				Complex 77) (46:46:8)		(350 Å)
				(400 Å)
Example 9	Compound	Compound	Compound	Compound	Compound	Compound
	HI	HT	H1	H1:Compound	H2	ET:Liq
	(100 Å)	(350 Å)	(50 Å)	H2:IrLa987(Lb3)2 (Metal	(100 Å)	(40:60)
				Complex 102) (46:46:8)		(350 Å)
				(400 Å)
Comparative	Compound	Compound	Compound	Compound	Compound	Compound
Example 1	HI	HT	H1	H1:Compound	H2	ET:Liq
	(100 Å)	(350 Å)	(50 Å)	H2:Comparative	(100 Å)	(40:60)
				compound 1 (46:46:8)		(350 Å)
				(400 Å)

The structures of the materials used in the device are as follows:

The IVL and lifetime characteristics of the device were measured at different current densities and voltages. Table 2 shows the data about the external quantum efficiency (EQE), kmax, full width at half maximum (FWHM), voltage (V), and CIE measured at 1000 nits.

TABLE 2
Device data
Device		λmax	FWHM	Voltage
number	CIE (x, y)	(nm)	(nm)	(V)	EQE (%)
Example 1	0.316, 0.645	523	53.9	2.76	23.62
Example 2	0.325, 0.644	526	42.5	2.76	24.81
Comparative	0.341, 0.630	528	59.3	2.98	22.52
Example 1

Table 3 shows the data about the external quantum efficiency (EQE), kmax, full width at half maximum (FWHM), voltage (V), and CIE of Examples 3 to 9 and Comparative Example 1 measured at 1000 nits. The lifetime (LT97) data of Examples 3 to 9 and Comparative Example 1 were tested at a constant current of 80 mA/cm².

TABLE 3
Device data
Device		λmax	FWHM	Voltage	EQE	LT97
number	CIE (x, y)	(nm)	(nm)	(V)	(%)	(h)
Example 3	0.341, 0.631	527	57.8	2.67	23.65	17.9
Example 4	0.345, 0.628	528	58.5	2.72	23.26	21.9
Example 5	0.339, 0.632	527	57.9	2.83	24.15	20.7
Example 6	0.326, 0.639	525	55.0	2.70	23.52	23.7
Example 7	0.345, 0.628	528	57.3	2.67	23.27	20.7
Example 8	0.346, 0.632	531	37.8	2.64	26.23	15.0
Example 9	0.346, 0.631	531	41.1	2.67	25.93	17.2
Comparative	0.341, 0.630	528	59.3	2.98	22.52	15.0
Example 1

Discussion:

As can be seen from Table 2, the device examples with the compounds of the present disclosure show several advantages over the comparative compound. Compared to Comparative Compound 1, the compounds of the present disclosure unexpectedly showed many characteristics, for example, in Examples 1 and 2, high efficiency of 23.62% and 24.81% EQE were achieved, respectively, and the voltage was more than 0.2 V lower than that of Comparative Compound 1 which contained no cyano substitution, and there was no noticeable blue-shifted or red-shifted light emission. The most unexpected is that they had a very narrow peak width of emitted light. In particular, the full width at half maximum of Example 2 was only 42.5 nm, which was unprecedented in green phosphorescent devices. These advantages will greatly help to improve the level and color saturation of green light devices.

As can be seen from Table 3, the device examples with the compounds of the present disclosure show several advantages over the comparative compound. Compared to Comparative Example 1, Examples 3-7 showed a higher EQE (23.25%-24.15% vs. 22.52%), and the life time was significantly better than Comparative Example 1 (17.9 h-23.7 h vs. 15 h). The life time of Example 6 was nearly 60% higher than that of Comparative Example 1 (23.7 h vs. 15 h), and the voltage was more than 0.2 V-0.3 V lower than that of Comparative Example 1 which contained no cyano substitution.

Compared with Comparative Example 1, Example 8 and Example 9 showed much higher EQE (26.23%, 25.93% vs. 22.52%), and a voltage drop exceeding 0.3 V (2.64 V-2.67 V vs. 2.98 V). The life time of Example 9 was 14.67% higher than that of Comparative Example 1 (17.2 h vs. 15 h). The most unexpected is that they had a very narrow peak width of emitted light. In particular, the full width at half maximum of Example 8 was only 37.8 nm, which was unprecedented in green phosphorescent devices.

Example 8 and Example 9 are comparisons of hydrogen and deuterated compounds at corresponding substitution positions. Example 9 has a longer lifespan than Example 8 and proves the advantages of deuterated compounds in the present disclosure.

It should be understood that the various embodiments described herein are merely examples and are not intended to limit the scope of the present disclosure. Therefore, as will be apparent to those skilled in the art, the claimed disclosure may include variations from the specific and preferred embodiments described herein. Many of the materials and structures described herein may be replaced with other materials and structures without departing from the spirit of the disclosure. It should be understood that various theories as to why the present disclosure works are not intended to be limiting.

Claims

1. A metal complex comprising a ligand La represented by Formula 1:

wherein,

Cy is any structure selected from the group consisting of:

R may represent mono-substitution, up to the maximum available multi-substitution, or no substitution; when more than one R exists in any structure, the R may be the same or different;

X1 to X4 are each independently selected from C, CRx1 or N, and at least one of X1 to X4 is C which is connected to the Cy; when more than one of X1 to X4 is CRx1, the Rx1 may be the same or different;

X5 to X8 are each independently selected from CRx2 or N; when more than one of X5 to X8 is CRx2, the Rx2 may be the same or different;

X is selected from the group consisting of O, S, Se, NRx3, CRx4Rx5 and SiRx6Rx7;

R, Rx1, Rx2, Rx3, Rx4, Rx5, Rx6 and Rx7 are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted arylalkyl group having 7-30 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted aryloxy group having 6-30 carbon atoms, a substituted or unsubstituted alkenyl group having 2-20 carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a substituted or unsubstituted arylsilyl group having 6-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof,

wherein, at least one of Rx1 and Rx2 is present and is a cyano group;

wherein, “#” represents a position at which the metal is connected, and “*” represents a position at which X1, X2, X3 or X4 is connected;

any two adjacent substituents can optionally be joined to form a ring;

X1, X2, X3 or X4 is connected to the metal through a metal-carbon bond or a metal-nitrogen bond.

2. The metal complex according to claim 1, wherein the Cy is

R may represent mono-substitution, up to the maximum available multi-substitution, or no substitution; when more than one R exists in any structure, the R may be the same or different;

R is each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted arylalkyl group having 7-30 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted aryloxy group having 6-30 carbon atoms, a substituted or unsubstituted alkenyl group having 2-20 carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a substituted or unsubstituted arylsilyl group having 6-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof,

wherein, “#” represents a position at which the metal is connected, and “*” represents a position at which X1, X2, X3 or X4 is connected;

any two adjacent substituents can optionally be joined to form a ring.

3. The metal complex according to claim 1, wherein the metal complex has a general formula of M(La)m(Lb)n(Lc)q, wherein La is a first ligand coordinated to the metal M, and the Lb and the Lc are a second ligand and a third ligand coordinated to the metal M, respectively, the Lb and the Lc may be the same or different;

the La, Lb and Lc can optionally be linked to form a multidentate ligand;

wherein, m is 1, 2 or 3, n is 0, 1 or 2, q is 0, 1 or 2, and m+n+q is equal to the oxidation state of M;

wherein, the metal M is selected from the group consisting of Cu, Ag, Au, Ru, Rh, Pd, Os, Ir, and Pt;

wherein, La is independently selected from the group consisting of:

wherein,

X is selected from the group consisting of O, S, Se, NRx3, CRx4Rx5 and SiRx6Rx7;

R1, R2, R3 and R4 may represent mono-, di-, tri- or tetra-substitution, or no substitution;

R1, R2, R3, R4, Rx3, Rx4, Rx5, Rx6 and Rx7 are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted arylalkyl group having 7-30 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted aryloxy group having 6-30 carbon atoms, a substituted or unsubstituted alkenyl group having 2-20 carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a substituted or unsubstituted arylsilyl group having 6-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof,

wherein, at least one of R3 and R4 is present and is a cyano group;

any two adjacent substituents can optionally be joined to form a ring;

wherein, the Lb and Lc are each independently selected from the group consisting of:

wherein,

Ra, Rb, and Rc may represent mono-, di-, tri- or tetra-substitution, or no substitution;

Xb is selected from the group consisting of: O, S, Se, NRN1, and CRC1RC2;

Ra, Rb, Rc, RN1, RC1 and RC2 are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted arylalkyl group having 7-30 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted aryloxy group having 6-30 carbon atoms, a substituted or unsubstituted alkenyl group having 2-20 carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a substituted or unsubstituted arylsilyl group having 6-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and

any two adjacent substituents can optionally be joined to form a ring.

4. The metal complex according to claim 3, wherein, the metal M is selected from Pt, Os or Ir.

5. The metal complex according to claim 3, wherein the metal complex has a structure represented by any one of Formulas 2 to 10:

wherein,

m is 1, 2 or 3;

X is selected from O, S or Se;

R1, R3, and R4 may represent mono-, di-, tri- or tetra-substitution, or no substitution;

Ra, Rb, and Rc may represent mono-, di-, tri- or tetra-substitution, or no substitution;

R1, R3, R4, Ra, Rb and Rc are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted arylalkyl group having 7-30 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted aryloxy group having 6-30 carbon atoms, a substituted or unsubstituted alkenyl group having 2-20 carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a substituted or unsubstituted arylsilyl group having 6-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

wherein, at least one of R3 and R4 is present and is a cyano group;

any two adjacent substituents can optionally be joined to form a ring.

6. The metal complex according to claim 5, wherein the metal complex has a structure of Formula 2-a:

wherein,

m is 1, 2 or 3;

X is selected from O, S or Se;

R3, and R4 may represent mono-, di-, tri- or tetra-substitution, or no substitution;

Ra, Rb, and Rc may represent mono-, di-, tri- or tetra-substitution, or no substitution;

wherein, R11, R12, R13, R14, R3, R4, Ra, and Rb are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted arylalkyl group having 7-30 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted aryloxy group having 6-30 carbon atoms, a substituted or unsubstituted alkenyl group having 2-20 carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a substituted or unsubstituted arylsilyl group having 6-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof,

wherein, at least one of R3 and R4 is present and is a cyano group;

any two adjacent substituents can optionally be joined to form a ring.

7. The metal complex according to claim 6, when R11 and R14 are both hydrogen, R12 and R13 are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, and the sum of carbon atoms in R12 and R13 is less than or equal to 1;

alternatively, when at least one of R11 and R14 is not hydrogen, R12 and R13 are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted heteroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted arylalkyl group having 7-30 carbon atoms, a substituted or unsubstituted alkoxy group having 1-20 carbon atoms, a substituted or unsubstituted aryloxy group having 6-30 carbon atoms, a substituted or unsubstituted alkenyl group having 2-20 carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a substituted or unsubstituted arylsilyl group having 6-20 carbon atoms, a substituted or unsubstituted amino group having 0-20 carbon atoms, an acyl group, a carbonyl group, a carboxylic acid group, an ester group, a cyano group, an isocyano group, thioalkyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.

8. The metal complex according to claim 6, wherein, R11, R12, R13, R14, Ra, and Rb are each independently selected from the group consisting of hydrogen, deuterium, halogen, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, and combinations thereof;

wherein, R3 and R4 are each independently selected from the group consisting of hydrogen, deuterium, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a cyano group, and combinations thereof,

wherein, at least one of R3 and R4 is present and is a cyano group.

9. The metal complex according to claim 1, wherein at least one of X5 to X8 in Formula 1 is CRx2, and the Rx2 is a cyano group.

10. The metal complex according to claim 1, wherein X5 to X8 are each independently selected from CRx2, and at least one of Rx2 is a cyano group.

11. The metal complex according to claim 1, wherein X7 is selected from CRx2, and the Rx2 is a cyano group; or X8 is selected from CRx2, and the Rx2 is a cyano group.

12. The metal complex according to claim 5, wherein R4 may represent mono-, di-, tri- or tetra-substitution; when more than one R4 exists, the R4 may be the same or different; R4 is selected from the group consisting of deuterium, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a cyano group, and combinations thereof, and at least one R4 is a cyano group.

13. The metal complex according to claim 5, wherein R4 may represent mono-, di-, tri- or tetra-substitution; when more than one R4 exists, the R4 may be the same or different; R4 is selected from the group consisting of deuterium, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, a substituted or unsubstituted aryl group having 6-30 carbon atoms, a substituted or unsubstituted heteroaryl group having 3-30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3-20 carbon atoms, a cyano group, and combinations thereof, and at least one R4 is a cyano group;

wherein R3 may represent mono-, di-substitution, or no substitution; R3 is selected from the group consisting of hydrogen, deuterium, a substituted or unsubstituted alkyl group having 1-20 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3-20 ring carbon atoms, and combinations thereof.

14. The metal complex according to claim 3, wherein the ligand La is selected from the group consisting of:

15. The metal complex according to claim 14, wherein the La can be partially or fully deuterated.

16. The metal complex according to claim 14, wherein the hydrogen on the aryl group in La can be partially or fully deuterated; and/or

wherein the hydrogen on the alkyl group in La can be partially or fully deuterated.

17. The metal complex according to claim 14, wherein the metal complex has the Formula IrLa(Lb)2 or Ir(La)2Lb, wherein La is one or two selected from La1 to La1019, and Lb is one or two selected from the group consisting of:

18. The metal complex according to claim 17, wherein the metal complex has the Formula Ir(La)2Lc or IrLa(Lc)2, wherein La is one or two selected from La1 to La1019, and Lc is one or two selected from the group consisting of:

19. The metal complex according to claim 18, wherein the metal complex has a structure represented by any one selected from the group consisting of Metal complex 1 to Metal complex 316: Metal Metal complex La Lb complex La Lb 1 La1 Lb1 2 La2 Lb1 3 La3 Lb1 4 La4 Lb1 5 La121 Lb1 6 La122 Lb1 7 La123 Lb1 8 La137 Lb1 9 La138 Lb1 10 La139 Lb1 11 La153 Lb1 12 La154 Lb1 13 La155 Lb1 14 La169 Lb1 15 La170 Lb1 16 La171 Lb1 17 La221 Lb1 18 La222 Lb1 19 La293 Lb1 20 La294 Lb1 21 La295 Lb1 22 La297 Lb1 23 La298 Lb1 24 La299 Lb1 25 La313 Lb1 26 La314 Lb1 27 La415 Lb1 28 La416 Lb1 29 La467 Lb1 30 La468 Lb1 31 La487 Lb1 32 La488 Lb1 33 La507 Lb1 34 La508 Lb1 35 La516 Lb1 36 La517 Lb1 37 La527 Lb1 38 La528 Lb1 39 La547 Lb1 40 La548 Lb1 41 La576 Lb1 42 La577 Lb1 43 La592 Lb1 44 La593 Lb1 45 La640 Lb1 46 La652 Lb1 47 La692 Lb1 48 La693 Lb1 49 La704 Lb1 50 La842 Lb1 51 La854 Lb1 52 La896 Lb1 53 La962 Lb1 54 La966 Lb1 55 La970 Lb1 56 La973 Lb1 57 La974 Lb1 58 La975 Lb1 59 La976 Lb1 60 La978 Lb1 61 La985 Lb1 62 La987 Lb1 63 La988 Lb1 64 La999 Lb1 65 La1003 Lb1 66 La1010 Lb1 67 La1 Lb3 68 La2 Lb3 69 La3 Lb3 70 La4 Lb3 71 La121 Lb3 72 La122 Lb3 73 La123 Lb3 74 La137 Lb3 75 La138 Lb3 76 La139 Lb3 77 La293 Lb3 78 La294 Lb3 79 La297 Lb3 80 La298 Lb3 81 La576 Lb3 82 La577 Lb3 83 La592 Lb3 84 La593 Lb3 85 La640 Lb3 86 La652 Lb3 87 La692 Lb3 88 La693 Lb3 89 La704 Lb3 90 La842 Lb3 91 La854 Lb3 92 La896 Lb3 93 La962 Lb3 94 La966 Lb3 95 La970 Lb3 96 La973 Lb3 97 La974 Lb3 98 La975 Lb3 99 La976 Lb3 100 La978 Lb3 101 La985 Lb3 102 La987 Lb3 103 La988 Lb3 104 La999 Lb3 105 La1003 Lb3 106 La1010 Lb3 107 La1 Lb 108 La2 Lb4 109 La3 Lb4 110 La4 Lb4 111 La121 Lb4 112 La122 Lb4 113 La123 Lb4 114 La137 Lb4 115 La138 Lb4 116 La139 Lb4 117 La293 Lb4 118 La294 Lb4 119 La297 Lb4 120 La298 Lb4 121 La576 Lb4 122 La577 Lb4 123 La592 Lb4 124 La593 Lb4 125 La640 Lb4 126 La652 Lb4 127 La692 Lb4 128 La693 Lb4 129 La704 Lb4 130 La842 Lb4 131 La854 Lb4 132 La896 Lb4 133 La962 Lb4 134 La966 Lb4 135 La970 Lb4 136 La973 Lb4 137 La974 Lb4 138 La975 Lb4 139 La976 Lb4 140 La978 Lb4 141 La985 Lb4 142 La987 Lb4 143 La988 Lb4 144 La999 Lb4 145 La1003 Lb4 146 La1010 Lb4 147 La1 Lb8 148 La2 Lb8 149 La3 Lb8 150 La4 Lb8 151 La121 Lb8 152 La122 Lb8 153 La123 Lb8 154 La137 Lb8 155 La138 Lb8 156 La139 Lb8 157 La293 Lb8 158 La294 Lb8 159 La297 Lb8 160 La298 Lb8 161 La576 Lb8 162 La577 Lb8 163 La592 Lb8 164 La593 Lb8 165 La640 Lb8 166 La652 Lbs 167 La692 Lb8 168 La693 Lb8 169 La704 Lb8 170 La842 Lb8 171 La854 Lb8 172 La896 Lb8 173 La962 Lb8 174 La966 Lb8 175 La970 Lb8 176 La973 Lb8 177 La974 Lb8 178 La975 Lb8 179 La976 Lb8 180 La978 Lb8 181 La985 Lb8 182 La987 Lb8 183 La988 Lb8 184 La999 Lb8 185 La1003 Lb8 186 La1010 Lb8 187 La1 Lb30 188 La2 Lb30 189 La3 Lb30 190 La4 Lb30 191 La121 Lb30 192 La122 Lb30 193 La123 Lb30 194 La137 Lb30 195 La138 Lb30 196 La139 Lb30 197 La293 Lb30 198 La294 Lb30 199 La297 Lb30 200 La298 Lb30 201 La576 Lb30 202 La577 Lb30 203 La592 Lb30 204 La593 Lb30 205 La640 Lb30 206 La652 Lb30 207 La692 Lb30 208 La693 Lb30 209 La704 Lb30 210 La842 Lb30 211 La854 Lb30 212 La896 Lb30 213 La962 Lb30 214 La966 Lb30 215 La970 Lb30 216 La973 Lb30 217 La974 Lb30 218 La975 Lb30 219 La976 Lb30 220 La978 Lb30 221 La985 Lb30 222 La987 Lb30 223 La988 Lb30 224 La999 Lb30 225 La1003 Lb30 226 La1010 Lb30 Metal Metal complex La Lc complex La Lc 227 La323 Lc1 228 La324 Lc1 229 La328 Lc1 230 La329 Lc1 231 La333 Lc1 232 La334 Lc1 233 La338 Lc1 234 La339 Lc1 235 La343 Lc1 236 La344 Lc1 237 La348 Lc1 238 La349 Lc1 239 La353 Lc1 240 La354 Lc1 241 La358 Lc1 242 La359 Lc1 243 La363 Lc1 244 La364 Lc1 245 La368 Lc1 246 La369 Lc1 247 La373 Lc1 248 La374 Lc1 249 La388 Lc1 250 La389 Lc1 251 La323 L31 252 La324 L31 253 La328 L31 254 La329 L31 255 La333 L31 256 La334 L31 257 La338 L31 258 La339 L31 259 La343 L31 260 La344 L31 261 La348 L31 262 La349 L31 263 La353 L31 264 La354 L31 265 La358 L31 266 La359 L31 267 La363 L31 268 La364 L31 269 La368 L31 270 La369 L31 271 La373 L31 272 La374 L31 273 La388 L31 274 La389 L31 Metal complex La 275 La1 276 La2 277 La3 278 La121 279 La122 280 La137 281 La138 282 La293 283 La297 284 La298 285 La487 286 La488 287 La507 288 La508 289 La547 290 La548 291 La576 292 La577 293 La640 294 La641 295 La652 296 La653 297 La692 298 La693 299 La704 300 La842 301 La854 302 La896 303 La962 304 La966 305 La970 306 La973 307 La974 308 La975 309 La976 310 La978 311 La985 312 La987 313 La988 314 La999 315 La1003 316 La1010

wherein, Metal complex 1 to Metal complex 226 have the structure of IrLa(Lb)2, wherein two Lb are the same, wherein La and Lb correspond to the structures as shown in the following table, respectively:

wherein, Metal complex 227 to Metal complex 274 have the structure of Ir(La)2Lc, wherein two La are the same, wherein La and Lc correspond to the structures as shown in the following table, respectively:

wherein, Metal complex 275 to Metal complex 316 have the structure of Ir(La)3, wherein three La are the same, wherein La corresponds to the structures as shown in the following table:

20. An electroluminescent device comprising:

an anode,

a cathode, and

an organic layer disposed between the anode and the cathode, wherein the organic layer includes the metal complex according to claim 1.

21. The electroluminescent device according to claim 20, wherein the organic layer is a light emitting layer, and the metal complex is a light emitting material.

22. The electroluminescent device according to claim 21, wherein the organic layer further comprises a host material; or, wherein the organic layer contains at least two host materials.

23. The electroluminescent device according to claim 22, wherein the host material comprises at least one chemical group selected from the group consisting of benzene, biphenyl, pyridine, pyrimidine, triazine, carbazole, azacarbazole, indolocarbazole, dibenzothiophene, azadibenzothiophen, dibenzofuran, azadibenzofuran, dibenzoselenophene, azadibenzoselenophene, triphenylene, azatriphenylene, fluorene, silicon-fluorene, naphthalene, quinoline, isoquinoline, quinazoline, quinoxaline, phenanthrene, azaphenanthrene, and combinations thereof.

24. The electroluminescent device according to claim 20, wherein the electroluminescent device is incorporated into a device selected from the group consisting of a consumption product, an electronic component module, an organic light-emitting device and a lighting panel.

25. A compound formulation comprising the metal complex according to claim 1.