Organic molecules for OLEDs and other optoelectronic devices

1. A composition comprising:

an organic emitter molecule for emission of light, comprising a ΔE(S 1 −T 1 ) value between a lowest excited singlet state (S 1 ) and a triplet state (T 1 ) below the lowest excited singlet state of less than 3000 cm −1 ; and

an optically inert atom or a molecule;

wherein the optically inert atom or molecule interacts with the organic emitter molecule to reduce an intersystem crossing time constant of the organic emitter molecule to less than 300 ms,

wherein the organic emitter molecule is a molecule of formula V:

wherein

at least one of D1 to D8 is hydrogen or represents a donor group, each independently selected from the group consisting of: —O(—), —NH-alkyl group, —N-(alkyl group) 2 , —NH 2 , —OH, —O-alkyl group, —NH(CO)alkyl group, —O(CO), -alkyl group, -aryl group, -heterocyclic groups —(CH)═C-(alkyl group) 2 , -phenoxazinyl, -phenothiazinyl, -carbazolyl, -dihydrophenazinyl, —N(R′)(R″) wherein R′ and R″ are H, alkyl, aryl, halogenated alkyl, halogenated aryl), wherein all aryl and heterocyclic groups can be substituted with alkyl and/or aryl groups, and all alkyl groups can also be substituted with F, Cl, Br and/or I;

wherein adjacent Di, Dj, and Dk from D1 to D8 optionally are conjugated aromatic or heteroaromatic rings, which may have a donor function, wherein i, j and k are each an integer from 1 to 8 and different from each other;

at least one of A1 to A8 is hydrogen or represents an acceptor group, each independently selected the group consisting of -halogen, —(CO)H, —(CO)-alkyl group, —(CO)O-alkyl group, —(CO)OH, —(CO)Cl, —CF 3 , —BF 2 , —CN, —S(O) 2 OH, —S(O) 2 O-alkyl, —NH 3 + , —N(alkyl group) 3 + , —NO 2 , halogenated alkyl, and —B(R′)(R″) wherein R′ and R″ are H, alkyl, aryl, halogenated alkyl, halogenated aryl;

wherein adjacent Ai, Aj, and Ak from A1 to A8 optionally are conjugated aromatic or heteroaromatic rings, which may have an acceptor function, wherein i, j and k are each an integer from 1 to 8 and different from each other;

at least one donor group and at least one acceptor group are present;

wherein the optically inert atom or molecule is selected from the group consisting of krypton, xenon, bromine-comprising substances, iodine-comprising substances, metal atoms, metal nanoparticles, metal ions, gadolinium-complexes and lead complexes, and

further wherein the organic emitter molecule is embedded into a matrix or cross-linked with a matrix and wherein the matrix comprises at least one covalently bonded additive selected from a bromine atom or an iodine atom.

2. The composition according to claim 1 , wherein the optically inert atom or molecule comprises a spin-orbit coupling constant of greater than 1000 cm −1 .

3. The composition according to claim 1 , wherein the ratio between the organic emitter molecule and the optically inert atom or molecule in the composition is in the range of 1:0.1 to 1:10.

4. The composition according to claim 1 , wherein the organic emitter molecule has at a temperature T=300 K, an emission decay time of less than 500 ms and an emission quantum yield of at least 30%.

5. The composition according to claim 1 , wherein the matrix comprises at least one deuterium atom.

6. The composition according to claim 1 , wherein the matrix is a polymer matrix or a polymer cross-linked matrix, and the matrix is covalently linked with the organic emitter molecule.

7. The composition of claim 1 , wherein the matrix comprises one of glucose, trehalose or a combination thereof.

8. The composition of claim 1 , wherein the composition is used in an emitter layer of an optoelectronic device.