Abstract: Provided is an organic electroluminescence device including a first electrode, a hole transport region disposed on the first electrode, an emission layer disposed on the hole transport region, an electron transport region disposed on the emission layer, and a second electrode disposed on the electron transport region. The emission layer includes a polycyclic compound represented by Formula 1, and thus the organic electroluminescence device exhibits high luminous efficiency.

Abstract: An organic electroluminescence device of one or more embodiments includes a first electrode, a hole transport region disposed on the first electrode, an emission layer disposed on the hole transport region, an electron transport region disposed on the emission layer and a second electrode disposed on the electron transport region, wherein the first electrode and the second electrode each independently includes at least one selected among Ag, Mg, Cu, Al, Pt, Pd, Au, Ni, Nd, Ir, Cr, Li, Ca, LiF/Ca, LiF/Al, Mo, Ti, In, Sn, Zn, compounds thereof, mixtures thereof, and oxides thereof, and the emission layer includes a polycyclic compound represented by Formula 1, thereby showing long life and high efficiency:

Abstract: An organic electroluminescence device of an embodiment includes a first electrode, a hole transport region disposed on the first electrode, an emission layer disposed on the hole transport region, an electron transport region disposed on the emission layer, and a second electrode disposed on the electron transport region, wherein the emission layer includes a polycyclic compound represented by Formula 1, thereby exhibiting high emission efficiency.

Abstract: An organic electroluminescence device of one or more embodiments includes a first electrode, a hole transport region disposed on the first electrode, an emission layer disposed on the hole transport region, an electron transport region disposed on the emission layer and a second electrode disposed on the electron transport region, wherein the emission layer includes a polycyclic compound represented by Formula 1, thereby showing high emission efficiency: wherein Y is O or S.

Abstract: An organic electroluminescence device includes a first electrode and a second electrode facing each other, and a plurality of organic layers disposed between the first electrode and the second electrode, wherein at least one of the plurality of organic layers includes a fused polycyclic compound represented by Formula 1, and the device exhibits improved luminous efficiency.

Abstract: An organic electroluminescence device includes a first electrode, a second electrode, and an emission layer disposed between the first electrode and the second electrode, wherein the emission layer includes a polycyclic compound having a fused ring system and represented by Formula 1 to achieve high efficiency and improved efficiency drop characteristics in an emission wavelength range:

Abstract: A novel compound which absorbs long-wavelength active energy rays and generates with high-efficiency radicals and strong bases, and which has excellent reaction efficiency in a base generating chain reaction; a photopolymerization initiator which contains said compound; and a photosensitive resin composition which contains said photopolymerization initiator are provided, where the novel compound is represented by formula (1), where, in formula (1), R1, R2, R3, R5 and R6 independently represent a hydroxyl group, an alkoxy group, or an organic group other than those substituents, the R4's independently represent an organic group including a thioether bond, ‘A’ represents a substituent represented by formula (1-1) or (1-2), where, in formula (1-1), R7 and R8 independently represent a hydrogen atom, an alkyl group or a heterocyclic group, and where, in formula (1-2), R9 and R10 independently represent an amino group or a substituted amino group.

Abstract: An organic electroluminescence device having high light emission efficiency is provided, which includes a first electrode, a second electrode facing the first electrode, and an emission layer disposed between the first electrode and the second electrode.

Abstract: An organic electroluminescence device exhibiting high light emission efficiency is provided, which includes a first electrode, a hole transport region disposed on the first electrode, an emission layer disposed on the hole transport region, an electron transport region disposed on the emission layer, and a second electrode disposed on the electron transport region.

Abstract: An organic electroluminescence device of an embodiment includes a first electrode, a second electrode, and a plurality of functional layers disposed between the first electrode and the second electrode, wherein at least one functional layer of the plurality of functional layers includes a polycyclic compound represented by Formula 1, thereby showing excellent light emitting efficiency in a short wavelength region:

Abstract: An organic electroluminescence device (OLED) of an embodiment includes a first electrode, a second electrode, and an emission layer disposed between the first electrode and the second electrode The emission layer may include a condensed polycyclic compound represented by Formula 1, which is connected to two or three substituents represented by Formula 2, and the OLED may exhibit excellent luminous efficiency:

Abstract: An organic electroluminescence device of an embodiment of the present disclosure includes a first electrode, a hole transport region disposed on the first electrode, an emission layer disposed on the hole transport region, an electron transport region disposed on the emission layer, and a second electrode disposed on the electron transport region.

Abstract: An organic electroluminescence device of an embodiment of the present disclosure includes a first electrode, a hole transport region on the first electrode, an emission layer on the hole transport region, an electron transport region on the emission layer, and a second electrode on the electron transport region, wherein the emission layer may include a polycyclic compound represented by Formula 1, thereby exhibiting high luminous efficiency: wherein at least one selected from R1 to R3 is represented by Formula 2:

Abstract: An organic electroluminescence device includes a first electrode, a hole transport region disposed on the first electrode, an emission layer disposed on the hole transport region, an electron transport region disposed on the emission layer, an electron transport region provided on the emission layer, and a second electrode disposed on the electron transport region, wherein the emission layer includes a polycyclic compound represented by Formula 1 to obtain high luminous efficiency:

Abstract: An organic electroluminescence device including a first electrode, a second electrode, and an emission layer between the first electrode and the second electrode, wherein the emission layer includes a compound represented by Formula 1 to achieve high efficiency and an improved efficiency drop in a deep blue emission wavelength region:

Abstract: An organic electroluminescence device of an embodiment includes a first electrode, a second electrode, and an emission layer between the first electrode and the second electrode, wherein the emission layer includes a polycyclic compound represented by Formula 1 below, and shows high emission efficiency:

Abstract: This compound, which absorbs long-wavelength active energy rays and generates with high-efficiency radicals and strong bases, and which has excellent reaction efficiency in a base generating chain reaction, is represented by formula (1), where, in formula (1), R1, R2, R3, R5 and R6 independently represent a hydroxy group, an alkoxy group, or an organic group other than those substituents, the R4's independently represent an organic group including a thioether bond, and ‘A’ represents a substituent represented by formula (1-1) or (1-2), where, in formula (1-1), R7 and R8 independently represent a hydrogen atom, an alkyl group or a heterocyclic group, and where, in formula (1-2), R9 and R10 independently represent an amino group or a substituted amino group. A photopolymerization initiator can include said compound; and a photosensitive resin composition can include said photopolymerization initiator.

Abstract: This base proliferating agent is represented by formula (1) or (2), where, in formulae (1) and (2), R1, R2, and R3 independently represent a hydrogen atom or a substituent and n independently represents an integer from 1 to 4. A base-reactive resin composition can include this base proliferating agent and a base-reactive compound.

Abstract: This compound which has excellent solvent solubility and compatibility with a resin, and which can generate bases and radicals with high efficiency by being irradiated with active energy rays, is represented by formula (1), where, in formula (1), R1, R2, R3, R5 and R6 represent a hydroxy group or an alkoxy group; the R4's independently represent an organic group containing a thioether bond; R7 and R9 independently represent a hydrogen atom or an alkyl group with 1 to 4 carbons; R8 represents an alkylene group or an arylene group; and X represents an oxygen atom or a sulfur atom. A photopolymerization initiator can include said novel compound; and a photosensitive resin composition can include said photopolymerization initiator, from which a cured product can be obtained that has high sensitivity and no metal corrosion.

Abstract: A compound represented by (Tr)n-Z is useful as a host material for delayed fluorescent materials. Tr represents a substituted or unsubstituted triphenylenyl group, and plural Tr's existing in the general formula (1) may be the same as or different from each other. Z represents a carbonyl group or a substituted or unsubstituted, n-valent aromatic hydrocarbon group. n represents an integer of 2 to 6, but when Z is a carbonyl group, n is 2.