Abstract: The invention relates to an organic molecule, in particular for the application in optoelectronic devices. According to the invention, the organic molecule has a structure represented by Formula I: wherein p and q are each an integer selected from 0 and 1, wherein p+q=1; r is at each occurrence an integer selected from 0, 1, 2, or 3; s is at each occurrence an integer selected from 0, 1, 2, 3, or 4; and Z is at each occurrence independently selected from the group consisting of a direct bond, CR3R4, C?CR3R4, C?O, C?NR3, NR3, O, SiR3R4, S, S(O), and S(O)2.

Abstract: An organic molecule for the application in optoelectronic devices is disclosed. The organic molecule has a first chemical moiety with a structure of Formula I: and independently at least one second chemical moiety with a structure of Formula II: wherein: X is independently N or CR1; Q is a C1-C40-alkyl; RT is independently selected from the group consisting of: Q, the binding site to a second chemical moiety, and C6-C60-aryl and C3-C57-heteroaryl, each of which is optionally substituted with one or more substituents selected from R1 and W; W represents the binding site to a second chemical moiety; # represents the binding site of the second chemical moiety to the first chemical moiety; and Z is at each occurrence independently from each other selected from the group consisting of a direct bond, CR3R4, C?CR3R4, C?O, C?NR3, NR3, O, SiR3R4, S, S(O), and S(O)2.

Abstract: The invention relates to an organic molecule for the use in optoelectronic devices. According to the invention, the organic molecule has a structure of Formula I: wherein: X is O or S; Z is independently selected from the group consisting of a direct bond, CR3R4, C?CR3R4, C?O, C?NR3, NR3, O, SiR3R4, S, S(O), and S(O)2; and Ra, R3, and R4 are independently selected from the group consisting of: hydrogen, deuterium, N(R5)2, OR5, Si(R5)3, B(OR5)2, B(R5)2, OSO2R5, CF3, CN, F, Br, I, C1-C40-alkyl, C1-C40-alkoxy, C1-C40-thioalkoxy, C2-C40-alkenyl, C2-C40-alkynyl, C6-C60-aryl, and C2-C57-heteroaryl.

Abstract: An organic molecule, for use in optoelectronic devices, has a structure represented by Formula I: with (L)n-RT, wherein L represents a substituted or unsubstituted aromatic ring; n is an integer, wherein n?1; RT represents the binding site between (L)n and the structure of Formula I at RC RC is selected from the group consisting of hydrogen, deuterium, N(Ra)2, ORa, Si(Ra)3, B(ORa)2, B(Ra)2, OSO2Ra, CF3, CN, F, Cl, Br, I, (L)n-RT, C1-C6-alkyl, and C6-C12-aryl, which is optionally substituted with one or more C1-C6-alkyl substituents; wherein at least one RC is (L)n-RT; at least one Rb is selected from the group consisting of C1-C6-alkyl and C6-C12-aryl; Ra1 is selected from the group consisting of: methyl, ipropyl, cyclo-hexyl, tbutyl, and phenyl; and Rd and Re are independently selected from the group consisting of: hydrogen, deuterium, N(Ra)2, ORa, Si(Ra)3, B(ORa)2, B(Ra)2, OSO2Ra, CF3, CN, F, Cl, Br, and I.

Abstract: The invention relates to an organic molecule, in particular for the application in optoelectronic devices. According to the invention, the organic molecule includes or consists of a structure represented by Formula I: wherein: p and q are each an integer selected from 0 and 1, wherein p+q=1; r is at each occurrence an integer selected from 0, 1, 2, or 3; s is at each occurrence an integer selected from 0, 1, 2, 3, or 4; and Z is at each occurrence independently selected from the group consisting of a direct bond, CR3R4, C?CR3R4, C?O, C?NR3, NR3, O, SiR3R4, S, S(O), and S(O)2.

Abstract: An open tri-dentate ligand L of Formula I is provided, wherein A1 is a N-heterocyclic group, which is optionally substituted by one or more substituents R1; A2 is a N-heterocyclic group, which is optionally substituted by one or more substituents R2; A3 is a N-heterocyclic group, which is optionally substituted by one or more substituents R3; A1, A2, and A3 are coordinated via the nitrogen atom of A1, A2, and A3 indicated by the dashed line

Abstract: The invention relates to an organic molecule, including or consisting of Formula A: wherein MTADF represents a thermally activated delayed fluorescence (TADF) moiety, L represents a direct bond or a divalent bridging unit that links MTADF and MBN and that is linked to MTADF and to MBN via a single bond each; and MBN represents an emitter moiety including a direct BN-bond. Furthermore, the present invention relates to the use of such organic molecule as a luminescent emitter in an optoelectronic device.

Abstract: The invention relates to an organic molecule, in particular for the application in optoelectronic devices. According to the invention, the organic molecule has of a structure of Formula I: wherein X1, X2, X3, X4, X5, X6, and X7 is independently selected from the group consisting of N and CRa, wherein Ra is at each occurrence independently selected from the group consisting of: hydrogen, deuterium, N(R5)2, OR5, Si(R5)3, B(OR5)2, B(R5)2, OSO2R5, CF3, CN, F, Br, I, C1-C40-alkyl, C1-C40-alkoxy, C1-C40-thioalkoxy, C2-C40-alkenyl, C2-C40-alkynyl, C6-C60-aryl, and C2-C57-heteroaryl.

Abstract: An organic molecule with a structure of Formula I is provided: Z is independently selected from the group consisting of a direct bond, NRa, O, and S; and Ra and Rb is independently selected from the group consisting of: hydrogen, deuterium, N(R5)2, OR5, Si(R5)3, B(OR5)2, B(R5)2, OSO2R5, CF3, CN, F, Br, I, C1-C40-alkyl, C1-C40-alkoxy, C1-C40-thioalkoxy, C2-C40-alkenyl, C2-C40-alkynyl, C6-C60-aryl, and C2-C57-heteroaryl.

Abstract: The invention relates to an organic molecule, in particular for the application in optoelectronic devices. According to the invention, the organic molecule has a structure of Formula I: wherein Rb is at each occurrence independently selected from the group consisting of Ra and a direct bond, which is formed with another group Rb; Ra is at each occurrence independently selected from the group consisting of: hydrogen, deuterium, N(R5)2, OR5, Si(R5)3, B(OR5)2, B(R5)2, OSO2R5, CF3, CN, F, Cl, Br, I, C1-C40-alkyl, C1-C40-alkoxy, C1-C40-thioalkoxy, C2-C40-alkenyl, C2-C40-alkynyl, C6-C60-aryl, and C2-C57-heteroaryl; and R5 is at each occurrence independently selected from the group consisting of: hydrogen, deuterium, N(R6)2, OR6, Si(R6)3, B(OR6)2, B(R6)2, OSO2R6, CF3, CN, F, Br, I, C1-C40-alkyl, C1-C40-alkoxy, C1-C40-thioalkoxy, C2-C40-alkenyl, C2-C40-alkynyl, C6-C60-aryl, and C2-C57-heteroaryl.

Abstract: The invention relates to an organic molecule, in particular for the application in optoelectronic devices. According to the invention, the organic molecule has a structure represented by Formula IVf wherein X is independently selected from the group consisting of a direct bond, CR3R4, C?CR3R4, C?O, C?NR3, NR3, O, SiR3R4, S, S(O), and S(O)2.

Abstract: An organic molecule for application in optoelectronic devices is disclosed. The organic molecule has a structure of Formula I, wherein R1 and R2 are independently from each other selected from the group consisting of: C1-C40-alkyl, which is optionally substituted with one or more substituents R5, and C6-C60-aryl, which is optionally substituted with one or more substituents R5; and RH is selected from the group consisting of H, D, F, Br, I, and C1-C4-alkyl.

Abstract: The invention relates to an organic molecule, in particular for the application in optoelectronic devices. According to the invention, the organic molecule has a structure of formula I wherein Ra is at each occurrence independently selected from the group consisting of: hydrogen, deuterium, N(R5)2, OR5, Si(R5)3, B(OR5)2, B(R5)2, OSO2R5, CF3, CN, F, Br, I, C1-C40-alkyl, C1-C40-alkoxy, C1-C40-thioalkoxy, C2-C40-alkenyl, C2-C40-alkynyl, C6-C60-aryl, and C2-C57-heteroaryl.

Abstract: An organic molecule and optoelectronic devices including the organic molecule are disclosed. The organic molecule has a structure of Formula I, where n, m, p, and q are integers selected from 0 and 1, wherein n+m=1 and p+q=1; Z is independently selected from the group consisting of a direct bond, CR3R4, C?CR3R4, C?O, C?NR3, NR3, O, SiR3R4, S, S(O) and S(O)2; R1 is independently selected from the group consisting of C1-C6-alkyl and C6-C12-aryl, which is optionally substituted with one or more C1-C6-alkyl substituents; and R2 is independently selected form the group consisting of hydrogen, deuterium, N(R5)2, OR5, Si(R5)3, C1-C40-alkyl, C6-C60-aryl, and C2-C57-heteroaryl.

Abstract: An organic molecule is disclosed, and an optoelectronic device including the organic molecule is disclosed. The organic molecule has a structure of Formula I, where n, m, p, and q are integers selected from 0 and 1, r is at each occurrence an integer selected from 0, 1, 2, 3 or 4; s is at each occurrence an integer selected from 0, 1, 2 or 3; t is an integer selected from 0, 1, 2, 3, or 4; u is an integer selected from 1, 2, 3, 4 or 5; wherein t+u<=5; Z is at each occurrence independently selected from the group consisting of a direct bond, CR3R4, C?CR3R4, C?O, C?NR3, NR3, O, SiR3R4, S, S(O) and S(O)2; and REWG is selected from the group consisting of F, CF3, CN, a substituted or unsubstituted C6-C60-aryl, and a substituted or unsubstituted C2-C57-heteroaryl.

Abstract: An organic molecule is represented by Formula I. In Formula 1, Ra is at each occurrence independently selected from the group consisting of: hydrogen, deuterium, N(R5)2, OR5, Si(R5)3, B(OR5)2, B(R5)2, OSO2R5, CF3, CN, F, Br, I, C1-C40-alkyl, C1-C40-alkoxy, C1-C40-thioalkoxy, C2-C40-alkenyl, C2-C40-alkynyl, C6-C60-aryl, and C2-C57-heteroaryl; and R5 is at each occurrence independently selected from the group consisting of: hydrogen, deuterium, N(R6)2, OR6, Si(R6)3, B(OR6)2, B(R6)2, OSO2R6, CF3, CN, F, Br, I, C1-C40-alkyl, C1-C40-alkoxy, C1-C40-thioalkoxy, C2-C40-alkenyl, C2-C40-alkynyl, C6-C60-aryl, and C2-C57-heteroaryl.

Abstract: An organic molecule for use in optoelectronic devices having a structure of formula I wherein X1 and X2 are at each occurrence independently selected from the group consisting of CR21 and N; X3 and X4 are at each occurrence independently selected from the group consisting of CR22 and N: X5 and X6 are at each occurrence independently selected from the group consisting of CR23 and N; R21, R22, R23 is at each occurrence independently selected from the group consisting of hydrogen, deuterium, C1-C5-alkyl, C2-C8-alkenyl, C2-C8-alkynyl, C6-C18-aryl, and C3-C17-heteroaryl; and at least one variable of X1 and X2 is N, at least one variable of X3 and X4 is N and at least one variable of X5 and X6 is N.

Abstract: The invention relates to an organic molecule, in particular for the application in optoelectronic devices. According to the invention, the organic molecule is represented by the following Formula I wherein: n=0 or 1; and X is selected from the group consisting of a direct bond, CR3R4, C?CR3R4, C?O, C?NR3, NR3, O, SiR3R4, S, S(O) and S(O)2; wherein at least one substituent RV forms a mono- or polycyclic, aliphatic, aromatic, heteroaromatic and/or benzo-fused ring system with one or more substituents R2 and/or RIV, wherein the ring system is selected from the following groups: wherein each dotted line indicates an attachment point.

Abstract: The invention relates to an organic molecule for use in optoelectronic devices. The organic molecule has a structure of Formula I: wherein X and Y are independently selected from the group consisting of a direct bond, N—R3, O, S, Si(R3)2 and C(R3)2; Z is a direct bond; m is 0 or 1; n is 0 or 1; is 0 or 1; R1 is independently selected from the group consisting of: hydrogen, deuterium, N(R3)2, OR3, SR3, Si(R3)3, B(OR3)2, OSO2R3, CF3, CN, halogen, C1-C40-alkyl, C1-C40-alkoxy, C1-C40-thioalkoxy, C2-C40-alkenyl, C2-C40-alkynyl, C6-C60-aryl; and Ra and R2 are independently selected from the group consisting of: hydrogen, deuterium, N(R3)2, OR3, SR3, Si(R3)3, B(OR3)2, OSO2R3, CF3, CN, halogen, C1-C40 alkyl, C1-C40-alkoxy, C1-C40-thioalkoxy, C2-C40-alkenyl, C2-C40-alkynyl, C6-C60-aryl; and C3-C57-heteroaryl.

Abstract: The invention pertains to an organic molecule for use in optoelectronic devices. According to the invention, the organic molecule has: a first chemical moiety with a structure of Formula I: one or two second chemical moieties with a structure of Formula 11: wherein RZ is the binding site of a single bond linking the first chemical moiety to the second moiety; RY is the binding site of a single bond linking the first chemical moiety to the second moiety or Ra; and the dashed lines “” represent the binding sites of the first chemical moiety to the second chemical moiety.