Polymeric, phosphorescent, organically semi-conductive emitter materials based on perarylated boranes, method for their production and use thereof

1. A phosphorescent copolyaryl borane of type K,

wherein:

x, y and z are molar parts and add up to 1 and the molar parts y and z each are >0,

hydrogen atoms are bonded at the ends,

M, HT and TE each represent a type of arylene component,

M is a matrix structure comprising an arylene structure, the arylene structure being any bivalently linking single- or multi-nucleic aromatic and/or heteroaromatic structure,

HT is a substituted 2-amino-thiophene or 2-amino-thiazole structure with hole-transport capability,

TE is a bivalent, phosphorescent organo-metallic complex of the following structure:

wherein Me denotes a metal of group 8, 9 or 10, Ar 5 is an arylene ligand that can form a complex with the metal Me and simultaneously is capable of polymeric linking,

TE does not have the ligand (L-X) if the metal Me is platinum, and for all other Me L-X is a complex-forming ligand, and

Ar is a carbocyclic or heterocyclic aryl moiety of which 0, 1 or more of the hydrogen atoms are each substituted by branched or linear aryl moieties or alkoxy moieties (C 1 to C 10 ), phenyl moieties or diphenyl or naphthylphenyl-amino groups.

2. The phosphorescent copolyaryl borane of claim 1 , wherein z has a value of between 0.01 and 0.1.

3. The phosphorescent copolyaryl borane of claim 1 , wherein the arylene structure M is a 2,7-fluorenylene structure that is unsubstituted, or is substituted in the 9-position with a linear or branched alkyl moiety (C 1 to C 10 ).

4. The phosphorescent copolyaryl borane of claim 1 , wherein the arylene structure M is a radical formed from one of the following groups a1 to x

the solubility of which in organic solvents is modifiable by arranging one or more of the linear or branched alkyl substituents or alkoxy substituents R, and also by the alkyl-substituted arylene substituent R 1 , or by the 2,7-disubstituted 9,9-dialkylfluorenylene structures that are substituted with branched or linear C 5 to C 10 alkyl groups.

5. The phosphorescent copolyaryl borane of claim 4 wherein, the substituted 2-amino-thiophene or 2-amino-thiazole structure HT with hole transport capacity is a structure selected from the group of structures HT(a) to HT(c), wherein

HT(a) is a substituted (2,2′-diamino-5,5′bisthienyl)-4,4′-ylene structure,

HT(b) is a substituted bis-N,N′-(thien-2-yl)- and/or bis-N,N′-(1,3-thiazol-2-yl) diaminoarylene structure, and

HT(c) is a substituted (2,2′-diamino)-bis-(4,4′thienyl)-arylene-5,5′-ylene structure, respectively in accordance with the formulas below,

and the substituents R 2 , R 3 and R 4 denote aryl groups Ar that in turn are unsubstituted or substituted by any additional arrangement of one or several linear or branched alkyl substituents or alkoxy substituents R, and the denotations of the substituents R n are identical for the same index n, and those of substituent R 1 are identical to the group for arylene structure M;

and for HT(b) X equals N or C-R

6. The phosphorescent copolyaryl borane of claim 1 wherein the carbocyclic or heterocyclic aryl moiety Ar is a group selected from the group consisting of: mesityl-, phenyl-, biphenylyl-, 1-naphthyl, 2-naphthyl-, 2-diphenyl-, 2-naphthylphenylamino-3,4-diphenyl-thien-5-yl-, 2-diphenyl-, and 2-naphthylphenylamino-3,4-diphenyl-1,3-thiazol-5-yl.

7. The phosphorescent copolyaryl borane of claim 1 wherein the bivalent phosphorescent organo-metallic complex TE has iridium as its central atom Me.

8. The phosphorescent copolyaryl borane of claim 1 wherein the bivalent phosphorescent organo-metallic complex TE is a radical selected from the group consisting of TE(a) to TE(g),

and ligand L-X is a ligand selected from the group consisting of complex-forming arylene ligands, 1,3-diketonate ligands, bis-thiazolylmethane or bis-thiazolylamine ligands, picolinate ligands, N-alkylsalicyclaldimino ligands and 8-hydroxyquinolate ligands.

9. The phosphorescent copolyaryl borane of claim 8 , wherein the ligand L-X is a ligand selected from the group consisting of a1, a2, a3, a4, a5, a6, a7, b1, b2, c1, c2, c3, c4, d, e and f

10. An organic light emitting diode, comprising copolyaryl borane of type K of claim 1 , wherein the copolyaryl borane is in a triplet-emitting and/or electron-transporting layer of the diode.

11. The phosphorescent copolyaryl borane of claim 1 , wherein Me is iridium, ruthenium, osmium or platinum.

12. A method for producing a phosphorescent copolyaryl borane of type K

wherein x, y and z are molar parts and add up to 1 and the molar parts y and z each are >0,

hydrogen atoms are bonded at the ends,

M, HT and TE each represent a type of arylene component,

M is a matrix structure comprising an arylene structure, the arylene structure being any bivalently linking single- or multi-nucleic aromatic and/or heteroaromatic structure,

HT is a substituted 2-amino-thiophene or 2-amino-thiazole structure with hole-transport capability,

TE is a bivalent, phosphorescent organo-metallic complex of the following structure:

wherein Me denotes a metal of group 8, 9 or 10, Ar 5 is an arylene ligand that can form a complex with the metal Me and simultaneously is capable of polymeric linking,

TE does not have the ligand (L-X) if the metal Me is platinum, and for all other Me L-X is a complex-forming ligand, and

Ar is a carbocyclic or heterocyclic aryl moiety of which 0, 1 or more of the hydrogen atoms are each substituted by branched or linear aryl moieties or alkoxy moieties (C 1 to C 10 ), phenyl moieties or diphenyl or naphthylphenyl-amino groups

in accordance with the general synthesis scheme:

wherein the starting point is the bromo-substituted arylene component M, the hole transport component HT and the bromo-substituted phosphorescent organo-metallic complex TE, the method comprising:

reversing the polarity of the component M, the component HT and the complex TE, either by way of a Grignard reaction or by lithiation to produce a magnesium halide compound or a lithiated compound;

after the reversing, substituting the magnesium or lithium of the magnesium halide compound or the lithiated compound with boron using a boron trihalide to form products H; and

in the products H of the substituting, substituting the halogens X on the boron with organic moieties Ar via a Grignard reagent or via a corresponding lithiated reagent.

13. A mixture of at least two different phosphorescing polyaryl boranes of type K, wherein in each individual component polymer two of the aspect ratio variables x, y or z have the value zero, wherein K has the following structure:

wherein:

hydrogen atoms are bonded at the ends,

M, HT and TE each represent a type of arylene component,

M is a matrix structure comprising an arylene structure, the arylene structure being any bivalently linking single- or multi-nucleic aromatic and/or heteroaromatic structure,

HT is a substituted 2-amino-thiophene or 2-amino-thiazole structure with hole-transport capability,

TE is a bivalent, phosphorescent organo-metallic complex of the following structure:

wherein Me denotes a metal of group 8, 9 or 10, Ar 5 is an arylene ligand that can form a complex with the metal Me and simultaneously is capable of polymeric linking,

TE does not have the ligand (L-X) if the metal Me is platinum, and for all other Me L-X is a complex-forming ligand, and

Ar is a carbocyclic or heterocyclic aryl moiety of which 0, 1 or more of the hydrogen atoms are each substituted by branched or linear aryl moieties or alkoxy moieties (C1 to C10), phenyl moieties or diphenyl or naphthylphenyl-amino groups

wherein the mixture is one of:

a homopolymer containing M and a homopolymer containing HT;

a homopolymer containg HT and a homopolymer containing TE;

a homopolymer containing M and a homopolymer containing TE; or

a homopolymer containing M, a homopolymer containing HT and a homopolymer containing TE.