Organic electronic devices comprising a layer comprising at least one metal organic compound and at least one metal oxide

1. An organic electronic device including a first electrode, a second electrode, and a first organic layer interposed between the first electrode and the second electrode, wherein the first organic layer comprises at least one metal organic compound and at least one metal oxide, wherein the at least one metal oxide comprises ReO 3 wherein the metal organic compound is a metal carbene complex of formula (I)

wherein the symbols have the following meanings:

M 1 is a metal atom selected from the group consisting of Rh, Ir, Pd, Pt, Ru, and Os, in any oxidation state possible for the respective metal atom;

carbene is a carbene ligand which may be uncharged or monoanionic and

monodentate, bidentate or tridentate, with the carbene ligand also being able to be a biscarbene or triscarbene ligand;

L is a monoanionic or dianionic ligand, which may be monodentate or bidentate;

K is an uncharged monodentate or bidentate ligand selected from the group consisting of phosphines; phosphonates and derivatives thereof, arsenates and derivatives thereof;

phosphites; CO; pyridines; nitriles and conjugated dienes which form a π complex with M 1 ;

n is the number of carbene ligands, where n is at least 1 and when n>1 the carbene ligands in the complex of the formula I can be identical or different;

m is the number of ligands L, where m can be 0 or ≧1 and when m>1 the ligands L can be identical or different;

o is the number of ligands K, where o can be 0 or ≧1 and when o>1 the ligands K can be identical or different;

where the sum n+m+o is dependent on the oxidation state and coordination number of the metal atom and on the denticity of the ligands carbene, L and K and also on the charge on the ligands, carbene and L, with the proviso that n is at least 1.

2. An organic electronic device according to claim 1 , wherein the metal oxide is employed in the first organic layer in an amount of from 0.1 to <10% by weight, based on the total weight of the first organic layer.

3. An organic electronic device according to claim 1 , wherein the metal carbene complex has the following formula

4. An organic electronic device according to claim 1 , wherein the first organic layer comprising at least one metal organic compound and at least one metal oxide is a hole transport layer or a hole injection layer.

5. An organic electronic device according to claim 1 additionally comprising a second organic layer comprising at least one compound of formula (II)

wherein

R 1 and R 2 are independently of each other F, C 1 -C 8 alkyl, or C 6 -C 14 aryl, which may optionally be substituted by one, or more C 1 -C 8 alkyl groups, or

two substituents R 1 and/or R 2 combine to form a fused benzene ring group, which may optionally be substituted by one, or more C 1 -C 8 alkyl groups,

a and b are independently of each other 0, or an integer 1 to 3,

M is an alkali metal atom, or an earth alkaline metal atom,

n is 1, if M is an alkali metal atom, n is 2, if M is an earth alkaline metal atom.

6. An organic electronic device according to claim 5 , wherein the second organic layer additionally comprises at least one compound of formula (III), (IVa) and/or (IVb)

wherein

R 81 , R 82 , R 83 , R 84 , R 81 ′, R 82 ′, R 83 ′, and R 84 ′ are independently of each other H, C 1 -C 18 alkyl, C 1 -C 18 alkyl which is substituted by E and/or interrupted by D, C 6 -C 24 aryl, C 6 -C 24 aryl which is substituted by G, C 2 -C 20 heteroaryl, or C 2 -C 20 heteroaryl which is substituted by G,

Q is an arylene or heteroarylene group, each of which may optionally be substituted by G;

D is —CO—; —COO—; —S—; —SO—; —SO 2 —; —O—; —NR 25 —; —SiR 30 R 31 —; —POR 32 —; —CR 23 ═CR 24 —; or —C≡C—; and

E is —OR 29 ; —SR 29 ; —NR 25 R 26 ; —COR 28 ; —COOR 27 ; —CONR 25 R 26 ; —CN; or F; G is E, C 1 -C 18 alkyl, C 1 -C 18 alkyl which is interrupted by D, C 1 -C 18 perfluoroalkyl, C 1 -C 18 alkoxy, or C 1 -C 18 alkoxy which is substituted by E and/or interrupted by D, wherein

R 23 and R 24 are independently of each other H, C 6 -C 18 aryl; C 6 -C 18 aryl which is substituted by C 1 -C 18 alkyl, or C 1 -C 18 alkoxy; C 1 -C 18 alkyl; or C 1 -C 18 alkyl which is interrupted by —O—;

R 25 and R 26 are independently of each other C 6 -C 18 aryl; C 6 -C 18 aryl which is substituted by C 1 -C 18 alkyl, or C 1 -C 18 alkoxy; C 1 -C 18 alkyl; or C 1 -C 18 alkyl which is interrupted by —O—; or

R 25 and R 26 together form a five or six membered ring, R 27 and R 28 are independently of each other C 6 -C 18 aryl; C 6 -C 18 aryl which is substituted by C 1 -C 18 alkyl, or C 1 -C 18 alkoxy; C 1 -C 18 alkyl; or C 1 -C 18 alkyl which is interrupted by —O—,

R 29 is C 6 -C 18 aryl; C 6 -C 18 aryl, which is substituted by C 1 -C 18 alkyl, or C 1 -C 18 alkoxy; C 1 -C 18 alkyl; or C 1 -C 18 alkyl which is interrupted by —O—,

R 30 and R 31 are independently of each other C 1 -C 18 alkyl, C 6 -C 18 aryl, or C 6 -C 18 aryl, which is substituted by C 1 -C 18 alkyl,

R 32 is C 1 -C 18 alkyl, C 6 -C 18 aryl, or C 6 -C 18 aryl, which is substituted by C 1 -C 18 alkyl;

wherein

R 89 is phenanthryl, pyrenyl, triphenylenyl, 1,10-phenanthrolinyl, triazinyl, dibenzothiophenyl, or pyrimidinyl, each of which may optionally be substituted by one, or more C 1 -C 18 alkyl, C 6 -C 14 aryl, or C 2 -C 20 heteroaryl groups,

R 90 is phenanthryl, pyrenyl, triphenylenyl, 1,10-phenanthrolinyl, triazinyl, dibenzothiophenyl, or pyrimidinyl, each of which may optionally be substituted by one, or more C 1 -C 18 alkyl, C 6 -C 14 aryl, or C 2 -C 20 heteroaryl groups,

R 91 is phenanthryl, pyrenyl, triphenylenyl, 1,10-phenanthrolinyl, triazinyl, dibenzothiophenyl, pyrimidinyl, or dibenzofuranyl, each of which may optionally be substituted by one, or more C 1 -C 18 alkyl, C 6 -C 14 aryl, or C 2 -C 20 heteroaryl groups,

R 92 is H, phenanthryl, pyrenyl, triphenylenyl, 1,10-phenanthrolinyl, triazinyl, dibenzothiophenyl, or pyrimidinyl, each of which may optionally be substituted by one, or more C 1 -C 18 alkyl, C 6 -C 14 aryl, or C 2 -C 20 heteroaryl groups,

A is a single bond, arylene, or heteroarylene group, each of which may optionally be substituted by one, or more C 1 -C 18 alkyl groups; or —SiR 87 R 88 —, wherein R 87 and R 88 are independently of each other C 1 -C 18 alkyl, or C 6 -C 14 aryl groups, which may optionally be substituted by one, or more C 1 -C 18 alkyl groups.

7. An organic electronic device according to claim 1 , wherein the organic electronic device is selected from the group consisting of an organic solar cell, a switching element and an organic light-emitting diode.

8. An organic electronic device according to claim 7 , wherein the organic electronic device is an OLED additionally comprising a light emitting layer comprising at least one phosphorescent light emitting material.

9. An organic electronic device according to claim 8 , wherein the light emitting layer additionally comprises at least one compound of formula (X) as host material

in which

T is NR 57 , S, O or PR 57 ;

R 57 is aryl, heteroaryl, alkyl, cycloalkyl or heterocycloalkyl;

Q′ is —NR 58 R 59 , —SiR 70 R 71 R 72 , —P(O)R 60 R 61 , —PR 62 R 63 , —S(O) 2 R 64 , —S(O)R 65 , —SR 66 or —OR 67 ;

R 55 , R 56 are each independently alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, SiR 70 R 71 R 72 , a Q′ group or a group with donor or acceptor action;

a″ is 0, 1, 2, 3 or 4;

b′ is 0, 1, 2 or 3;

R 58 , R 59 form, together with the nitrogen atom, a cyclic radical which has 3 to ring atoms and may be unsubstituted or substituted by one or more substituents selected from alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl and a group with donor or acceptor action, and/or may be fused to one or more further cyclic radicals having 3 to 10 ring atoms, where the fused radicals may be unsubstituted or substituted by one or more substituents selected from alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl and a group with donor or acceptor action;

R 70 , R 71 , R 72 , R 60 , R 61 , R 62 , R 63 , R 64 , R 65 , R 66 , R 67

are each independently aryl, heteroaryl, alkyl, cycloalkyl or heterocycloalkyl,

or

two units of the general formula (X) are bridged to one another via a linear or branched, saturated or unsaturated bridge optionally interrupted by at least one heteroatom, via a bond or via O.

10. An organic electronic device according to claim 8 , wherein the light emitting layer additionally comprises at least one compound of formula (V) as host material

wherein

X is NR, S, O or PR;

R is aryl, heteroaryl, alkyl, cycloalkyl, or heterocycloalkyl;

A is —NR 6 R 7 , —P(O)R 8 R 9 , —PR 10 R 11 , —S(O) 2 R 12 , —S(O)R 13 , —SR 14 , or —OR 15 ;

R 1 , R 2 and R 3 are independently of each other aryl, heteroaryl, alkyl, cycloalkyl, or heterocycloalkyl, wherein at least on of the groups R 1 , R 2 , or R 3 is aryl, or heteroaryl;

R 4 and R 5 are independently of each other alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, a group A, or a group having donor, or acceptor characteristics;

n and m are independently of each other 0, 1, 2, or 3;

R 6 , R 7 form together with the nitrogen atom a cyclic residue having 3 to 10 ring atoms, which can be unsubstituted, or which can be substituted with one, or more substituents selected from alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl and a group having donor, or acceptor characteristics; and/or which can be annulated with one, or more further cyclic residues having 3 to 10 ring atoms, wherein the annulated residues can be unsubstituted, or can be substituted with one, or more substituents selected from alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl and a group having donor, or acceptor characteristics; and

R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 and R 15 are independently of each other aryl, heteroaryl, alkyl, cycloalkyl, or heterocycloalkyl.

11. An apparatus comprising the organic electronic device according to claim 1 .

12. A hole transport layer or a hole injection layer comprising at least one metal organic compound and at least one metal oxide, wherein the at least one metal oxide comprises ReO 3 wherein the metal organic compound is a metal carbene complex of formula (I)

wherein the symbols have the following meanings:

M 1 is a metal atom selected from the group consisting of Rh, Ir, Pd, Pt, Ru, and Os, in any oxidation state possible for the respective metal atom;

carbene is a carbene ligand which may be uncharged or monoanionic and

monodentate, bidentate or tridentate, with the carbene ligand also being able to be a biscarbene or triscarbene ligand;

L is a monoanionic or dianionic ligand, which may be monodentate or bidentate;

K is an uncharged monodentate or bidentate ligand selected from the group consisting of phosphines; phosphonates and derivatives thereof, arsenates and derivatives thereof;

phosphites; CO; pyridines; nitriles and conjugated dienes which form a π complex with M 1 ;

n is the number of carbene ligands, where n is at least 1 and when n>1 the carbene ligands in the complex of the formula I can be identical or different;

m is the number of ligands L, where m can be 0 or ≧1 and when m>1 the ligands L can be identical or different;

o is the number of ligands K, where o can be 0 or ≧1 and when o>1 the ligands K can be identical or different;

where the sum n+m+o is dependent on the oxidation state and coordination number of the metal atom and on the denticity of the ligands carbene, L and K and also on the charge on the ligands, carbene and L, with the proviso that n is at least 1.

13. An organic electronic device including a first electrode, a second electrode, and a first organic layer interposed between the first electrode and the second electrode, wherein the first organic layer comprises at least one metal organic compound and ReO 3 wherein the metal organic compound is a metal carbene complex of formula (I)

wherein the symbols have the following meanings:

M 1 is a metal atom selected from the group consisting of Rh, Ir, Pd, Pt, Ru, and Os, in any oxidation state possible for the respective metal atom;

carbene is a carbene ligand which may be uncharged or monoanionic and

monodentate, bidentate or tridentate, with the carbene ligand also being able to be a biscarbene or triscarbene ligand;

L is a monoanionic or dianionic ligand, which may be monodentate or bidentate;

K is an uncharged monodentate or bidentate ligand selected from the group consisting of phosphines; phosphonates and derivatives thereof, arsenates and derivatives thereof;

phosphites; CO; pyridines; nitriles and conjugated dienes which form a π complex with M 1 ;

n is the number of carbene ligands, where n is at least 1 and when n>1 the carbene ligands in the complex of the formula I can be identical or different;

m is the number of ligands L, where m can be 0 or ≧1 and when m>1 the ligands L can be identical or different;

o is the number of ligands K, where o can be 0 or ≧1 and when o>1 the ligands K can be identical or different;

where the sum n+m+o is dependent on the oxidation state and coordination number of the metal atom and on the denticity of the ligands carbene, L and K and also on the charge on the ligands, carbene and L, with the proviso that n is at least 1.