Aminostyryl compound, method of preparing the same, and organic light emitting device using the aminostyryl compound

1. An aminostyryl compound represented by Formula 1:

where Ar 1 and Ar 2 are each independently a substituted or unsubstituted C 6 -C 30 aryl group, or a substituted or unsubstituted C 2 -C 30 heteroaryl group;

R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 are each independently hydrogen, a substituted or unsubstituted C 1 -C 20 alkyl group, or a substituted or unsubstituted C 1 -C 20 alkoxy group;

n is 1, 2 or 3; and

L is selected from the group consisting of a C 1 -C 10 alkylphenyl group, a C 1 -C 10 alkoxyphenyl group, a halophenyl group, a cyanophenyl group, a dicyanophenyl group, a trifluoromethoxyphenyl group, o-, m-, or p-tolyl group, o-, m- or p-cumenyl group, a mesityl group, a phenoxyphenyl group, a (α,α-dimethylbenzen)phenyl group, a (N,N′-dimethyl)aminophenyl group, a (N,N-diphenyl)aminophenyl group, a (C 1 -C 10 alkylcyclohexyl)phenyl group, a (anthracenyl)phenyl group, a C 1 -C 10 alkylbiphenyl group, a C 1 -C 10 alkoxybiphenyl group, a pentalenyl group, an indenyl group, a C 1 -C 10 alkylnaphtyl group, a C 1 -C 10 alkoxynaphtyl group, a halonaphtyl group, a cyanonaphtyl group, a biphenylenyl group, a C 1 -C 10 alkyl biphenylenyl group, a C 1 -C 10 alkoxy biphenylenyl group, an azulenyl group, a heptalenyl group, an acenaphtylenyl group, a phenalenyl group, an anthraquinolyl group, a methylanthryl group, a phenanthrenyl group, a triphenylenyl group, a chrysenyl group, an ethyl-chrysenyl group, a picenyl group, a perylenyl group, a chloroperylenyl group, a pentaphenyl group, a pentacenyl group, a tetraphenylenyl group, a hexaphenyl group, a hexacenyl group, a rubicenyl group, a coronenyl group, a trinaphthylenyl group, a heptaphenyl group, a heptacenyl group, a pyranthrenyl group, an ovalenyl group, a C 1-10 alkyl carbazolyl group, an indolyl group, a purinyl group, a benzimidazolyl group, a benzothiophenyl group, a parathiazinyl group, a pyrroyl group, a pyrazolyl group, an imidazolyl group, an imidazolinyl group, an oxazolyl group, a thiozolyl group, a triazolyl group, a tetrazolyl group, an oxadiazolyl group, a pyridazinyl group, a pyrimidinyl group, a pyrazinyl group, a thianthrenyl group, a cyclopentyl group, a cyclohexyl group, a C 1 -C 10 alkylcyclohexyl group, a C 1 -C 10 alkoxycyclohexyl group, an oxyranyl group, a pyrrolidinyl group, a pyrazolidinyl group, an imidazolidinyl group, a piperidinyl group, a piperazinyl group, and a morpholinyl group.

2. The aminostyryl compound of claim 1 , wherein substituents of the substituted C 6 -C 30 aryl group, the substituted C 2 -C 30 heteroaryl group, the substituted C 1 -C 20 alkyl group, the substituted C 1 -C 20 alkoxy group, comprise at least one selected from the group consisting of —F, —Cl, —Br, —CN, —NO 2 , —OH, a C 1 -C 20 alkyl group that is unsubstituted or substituted with —F, —Cl, —Br, —CN, —NO 2 or —OH, a C 1 -C 20 alkoxy group that is unsubstituted or substituted with —F, —Cl, —Br, —CN, —NO 2 or —OH, a C 6 -C 30 aryl group that is unsubstituted or substituted with —F, —Cl, —Br, —CN, —NO 2 or —OH, a C 2 -C 30 heteroaryl group that is unsubstituted or substituted with —F, —Cl, —Br, —CN, —NO 2 or —OH, a C 5 -C 20 cycloalkyl group that is unsubstituted or substituted with —F, —Cl, —Br, —CN, —NO 2 or —OH, and a C 5 -C 30 heterocycloalkyl group that is unsubstituted or substituted with —F, —Br, —CN, —NO 2 or —OH.

3. The aminostyryl compound of claim 1 , wherein Ar 1 and Ar 2 are each independently selected from the group consisting of a phenyl group, a C 1 -C 10 alkylphenyl group, a C 1 -C 10 alkoxyphenyl group, a halophenyl group, a cyanophenyl group, a dicyanophenyl group, a trifluoromethoxyphenyl group, o-, m-, or p-tolyl group, o-, m- or p-cumenyl group, a mesityl group, a phenoxyphenyl group, a (α,α-dimethylbenzen)phenyl group, a (N,N′-dimethyl)aminophenyl group, a (N,N-diphenyl)aminophenyl group, a (C 1 -C 10 alkylcyclohexyl)phenyl group, a (anthracenyl)phenyl group, a biphenyl group, a C 1 -C 10 alkylbiphenyl group, a C 1 -C 10 alkoxybiphenyl group, a pentalenyl group, an indenyl group, a naphtyl group, a C 1 -C 10 alkylnaphtyl group, a C 1 -C 10 alkoxynaphtyl group, a halonaphtyl group, a cyanonaphtyl group, a biphenylenyl group, a C 1 -C 10 alkyl biphenylenyl group, a C 1 -C 10 alkoxy biphenylenyl group, an anthracenyl group, an azulenyl group, a heptalenyl group, an acenaphtylenyl group, a phenalenyl group, a fluorenyl group, an anthraquinolyl group, a methylanthryl group, a phenanthrenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, an ethyl-chrysenyl group, a picenyl group, a perylenyl group, a chloroperylenyl group, a pentaphenyl group, a pentacenyl group, a tetraphenylenyl group, a hexaphenyl group, a hexacenyl group, a rubicenyl group, a coronenyl group, a trinaphthylenyl group, a heptaphenyl group, a heptacenyl group, a pyranthrenyl group, an ovalenyl group, a carbazolyl group, a C 1-10 alkyl carbazolyl group, a thiophenyl group, an indolyl group, a purinyl group, a benzimidazolyl group, a quinolinyl group, a benzothiophenyl group, a parathiazinyl group, a pyrroyl group, a pyrazolyl group, an imidazolyl group, an imidazolinyl group, an oxazolyl group, a thiozolyl group, a triazolyl group, a tetrazolyl group, an oxadiazolyl group, a pyridinyl group, a pyridazinyl group, a pyrimidinyl group, a pyrazinyl group, and a thianthrenyl group.

4. The aminostyryl compound of claim 1 , wherein n is one of 1 or 2.

5. The aminostyryl compound of claim 1 , represented by one of the following formulas:

6. An organic light emitting device comprising at least an organic layer interposed between a first electrode and a second electrode, said at least an organic layer formed of the aminostyryl compound of claim 1 .

7. A method of preparing a compound represented by Formula 1 of claim 1 , the method comprising:

reacting a compound represented by Formula 1a with a compound represented by Formula 1b to produce a compound represented by Formula 1c; and

reacting the compound represented by Formula 1c with compounds represented by Formula 1d to produce the compound represented by Formula 1:

where Ar 1 and Ar 2 are each independently a substituted or unsubstituted C 6 -C 30 aryl group, or a substituted or unsubstituted C 2 -C 30 heteroaryl group;

R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 are each independently hydrogen, a substituted or unsubstituted C 1 -C 20 alkyl group, or a substituted or unsubstituted C 1 -C 20 alkoxy group;

n is 1, 2 or 3;

L is a substituted or unsubstituted C 6 -C 30 aryl group, a substituted or unsubstituted C 2 -C 30 heteroaryl group, a substituted or unsubstituted C 5 -C 20 cycloalkyl group, or a substituted or unsubstituted C 5 -C 30 heterocycloalkyl group;

Ha is halogen; and

Q is a B-containing group.

8. The method of claim 7 , wherein Q is one of

9. The method of claim 7 , wherein the aminostyryl compound is represented by one of the following formula:

10. A compound prepared by the method of claim 7 .

11. An organic light emitting device, comprising:

a first electrode;

a second electrode; and

at least an organic layer interposed between the first electrode and the second electrode, said at least an organic layer comprising an organic layer formed of an aminostyryl compound represented by Formula 1:

where Ar 1 and Ar 2 are each independently a substituted or unsubstituted C 6 -C 30 aryl group, or a substituted or unsubstituted C 2 -C 30 heteroaryl group;

R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 are each independently hydrogen, a substituted or unsubstituted C 1 -C 20 alkyl group, or a substituted or unsubstituted C 1 -C 20 alkoxy group;

n is 1, 2 or 3; and

L selected from the group consisting of a C 1 -C 10 alkylphenyl group, a C 1 -C 10 alkoxyphenyl group, a halophenyl group, a cyanophenyl group, a dicyanophenyl group, a trifluoromethoxyphenyl group, o-, m-, or p-tolyl group, o-, m- or p-cumenyl group, a mesityl group, a phenoxyphenyl group, a (α,α-dimethylbenzen)phenyl group, a (N,N′-dimethyl)aminophenyl group, a (N,N-diphenyl)aminophenyl group, a (C 1 -C 10 alkylcyclohexyl)phenyl group, a (anthracenyl)phenyl group, a C 1 -C 10 alkylbiphenyl group, a C 1 -C 10 alkoxybiphenyl group, a pentalenyl group, an indenyl group, a C 1 -C 10 alkylnaphtyl group, a C 1 -C 10 alkoxynaphtyl group, a halonaphtyl group, a cyanonaphtyl group, a biphenylenyl group, a C 1 -C 10 alkyl biphenylenyl group, a C 1 -C 10 alkoxy biphenylenyl group, an azulenyl group, a heptalenyl group, an acenaphtylenyl group, a phenalenyl group, an anthraquinolyl group, a methylanthryl group, a phenanthrenyl group, a triphenylenyl group, a chrysenyl group, an ethyl-chrysenyl group, a picenyl group, a perylenyl group, a chloroperylenyl group, a pentaphenyl group, a pentacenyl group, a tetraphenylenyl group, a hexaphenyl group, a hexacenyl group, a rubicenyl group, a coronenyl group, a trinaphthylenyl group, a heptaphenyl group, a heptacenyl group, a pyranthrenyl group, an ovalenyl group, a C 1-10 alkyl carbazolyl group, an indolyl group, a purinyl group, a benzimidazolyl group, a benzothiophenyl group, a parathiazinyl group, a pyrroyl group, a pyrazolyl group, an imidazolyl group, an imidazolinyl group, an oxazolyl group, a thiozolyl group, a triazolyl group, a tetrazolyl group, an oxadiazolyl group, a pyridazinyl group, a pyrimidinyl group, a pyrazinyl group, a thianthrenyl group, a cyclopentyl group, a cyclohexyl group, a C 1 -C 10 alkylcyclohexyl group, a C 1 -C 10 alkoxycyclohexyl group, an oxyranyl group, a pyrrolidinyl group, a pyrazolidinyl group, an imidazolidinyl group, a piperidinyl group, a piperazinyl group, and a morpholinyl group.

12. The organic light emitting device of claim 11 , wherein the organic layer formed of the aminostyryl compound is an emissive layer.

13. The organic light emitting device of claim 11 , wherein the organic layer formed of the aminostyryl compound is a hole transport layer.

14. The organic light emitting device of claim 11 , wherein said at least one organic layer comprises at least one layer selected from the group consisting of a hole injection layer, a hole transport layer, an electron blocking layer, a hole blocking layer, an electron transport layer, and an electron injection layer.

15. The organic light emitting device of claim 11 , wherein said at least one organic layer comprises a hole injection layer formed on the first electrode, an emissive layer formed on the hole injection layer, an electron transport layer formed on the emissive layer, an electron injection layer formed on the electron transport layer.

16. The organic light emitting device of claim 15 , wherein said at least one organic layer further comprises a hole transport layer between the hole injection layer and the emissive layer.

17. The organic light emitting device of claim 16 , wherein said at least one organic layer further comprises a hole blocking layer between the emissive layer and the electron transport layer.

18. The organic light emitting device of claim 12 , wherein the emissive layer comprises at least one dopant selected from the group consisting of a red phosphorescent dopant, a green phosphorescent dopant, a blue phosphorescent dopant, a white phosphorescent dopant, a red fluorescent dopant, a green fluorescent dopant, a blue fluorescent dopant, and a white fluorescent dopant.

19. The organic light emitting device of claim 11 , wherein the aminostyryl compound is represented by one of the following formulas: