Organometallic complex, method of preparing the same and organic light emitting device comprising the same
View Patent ↗An organometallic complex for an organic light emitting device represented by formula 1, a method of preparing the same and an organic light emitting device including the same: where R 1 through R 16 are a hydrogen atom, a cyano group, a hydroxyl group, a nitro group, a halogen atom, a C 1 -C 20 alkyl group, a C 1 -C 20 alkoxy group, a C 6 -C 20 aryl group, a C 7 -C 20 arylalkyl group, a C 2 -C 20 alkylalkoxy group, a C 7 -C 20 arylalkoxy group, a C 6 -C 20 arylamino group, a C 1 -C 20 alkylamino group, a C 6 -C 20 heteroarylamino group, and a C 2 -C 20 hetero-ring group; and M is a bivalent metal such as Be, Mg, Zn, Ca, Cr, Fe, Co, Ni and Cu. The compound represented by Formula 1 can be effectively used in an electron transport layer or an electron injection layer. An organic light emitting device including the compound represented by Formula 1 can thus have long lifetime.
1. An organometallic complex represented by Formula 1:
where R 1 through R 16 are each independently selected from the group consisting of a hydrogen atom, a cyano group, a hydroxyl group, a nitro group, a halogen atom, a substituted or unsubstituted C 1 -C 20 alkyl group, a substituted or unsubstituted C 1 -C 20 alkoxy group, a substituted or unsubstituted C 6 -C 20 aryl group, a substituted or unsubstituted C 7 -C 20 arylalkyl group, a substituted or unsubstituted C 2 -C 20 alkylalkoxy group, a substituted or unsubstituted C 7 -C 20 arylalkoxy group, a substituted or unsubstituted C 6 -C 20 arylamino group, a substituted or unsubstituted C 1 -C 20 alkylamino group, a substituted or unsubstituted C 6 -C 20 heteroarylamino group, and a substituted or unsubstituted C 2 -C 20 hetero-ring group; and
M is a bivalent metal selected from the group consisting of Be, Mg, Zn, Ca, Cr, Fe, Co, Ni and Cu.
2. The organometallic complex of claim 1 , represented by one selected from the group consisting of Formulae 2 through 7:
where M is a bivalent metal selected from the group consisting of Be, Mg, Zn, Ca, Cr, Fe, Co, Ni and Cu; and
R 17 and R 18 are each independently selected from the group consisting of a hydrogen atom, a cyano group, a hydroxyl group, a nitro group, a halogen atom, a substituted or unsubstituted C 1 -C 20 alkyl group, a substituted or unsubstituted C 1 -C 20 alkoxy group, a substituted or unsubstituted C 6 -C 20 aryl group, a substituted or unsubstituted C 7 -C 20 arylalkyl group, a substituted or unsubstituted C 2 -C 20 alkylalkoxy group, a substituted or unsubstituted C 7 -C 20 arylalkoxy group, a substituted or unsubstituted C 6 -C 20 arylamino group, a substituted or unsubstituted C 1 -C 20 alkylamino group, a substituted or unsubstituted C 6 -C 20 heteroarylamino group, and a substituted or unsubstituted C 2 -C 20 hetero-ring group.
3. The organometallic complex of claim 1 , represented by Formula 8:
4. The organometallic complex of claim 1 , represented by Formula 9:
5. The organometallic complex of claim 1 , represented by Formula 10:
6. An organic light emitting device comprising at least one organic layer comprised of the organometallic complex of claim 1 .
7. A method of preparing an organometallic complex represented by Formula 1, the method comprising:
reacting benzoquinolinol derivatives (A) and (A′) and a bivalent metal complex (B):
where R 1 through R 16 are each independently selected from the group consisting of a hydrogen atom, a cyano group, a hydroxyl group, a nitro group, a halogen atom, a substituted or unsubstituted C 1 -C 20 alkyl group, a substituted or unsubstituted C 1 -C 20 alkoxy group, a substituted or unsubstituted C 6 -C 20 aryl group, a substituted or unsubstituted C 7 -C 20 arylalkyl group, a substituted or unsubstituted C 2 -C 20 alkylalkoxy group, a substituted or unsubstituted C 7 -C 20 arylalkoxy group, a substituted or unsubstituted C 6 -C 20 arylamino group, a substituted or unsubstituted C 1 -C 20 alkylamino group, a substituted or unsubstituted C 6 -C 20 heteroarylamino group, and a substituted or unsubstituted C 2 -C 20 hetero-ring group;
M is a bivalent metal selected from the group consisting of Be, Mg, Zn, Ca, Cr, Fe, Co, Ni and Cu, and
L is a monovalent anion ligand.
8. The method of claim 7 , wherein the compound (A) is prepared by reacting a naphthalene derivative (C) and a glycerol derivative (D) in the presence of an acid as shown below:
where R 1 through R 8 are each independently selected from the group consisting of a hydrogen atom, a cyano group, a hydroxyl group, a nitro group, a halogen atom, a substituted or unsubstituted C 1 -C 20 alkyl group, a substituted or unsubstituted C 1 -C 20 alkoxy group, a substituted or unsubstituted C 6 -C 20 aryl group, a substituted or unsubstituted C 7 -C 20 arylalkyl group, a substituted or unsubstituted C 2 -C 20 alkylalkoxy group, a substituted or unsubstituted C 7 -C 20 arylalkoxy group, a substituted or unsubstituted C 6 -C 20 arylamino group, a substituted or unsubstituted C 1 -C 20 alkylamino group, a substituted or unsubstituted C 6 -C 20 heteroarylamino group, and a substituted or unsubstituted C 2 -C 20 hetero-ring group.
9. The method of claim 7 , wherein the compound (A′) is prepared by reacting a naphthalene derivative (C′) and a glycerol derivative (D′) in the presence of an acid as shown below:
where R 9 through R 16 are each independently selected from the group consisting of a hydrogen atom, a cyano group, a hydroxyl group, a nitro group, a halogen atom, a substituted or unsubstituted C 1 -C 20 alkyl group, a substituted or unsubstituted C 1 -C 20 alkoxy group, a substituted or unsubstituted C 6 -C 20 aryl group, a substituted or unsubstituted C 7 -C 20 arylalkyl group, a substituted or unsubstituted C 2 -C 20 alkylalkoxy group, a substituted or unsubstituted C 7 -C 20 arylalkoxy group, a substituted or unsubstituted C 6 -C 20 arylamino group, a substituted or unsubstituted C 1 -C 20 alkylamino group, a substituted or unsubstituted C 6 -C 20 heteroarylamino group, and a substituted or unsubstituted C 2 -C 20 hetero-ring group.
10. The method of claim 7 , wherein L of the bivalent metal complex (B) is R′COO − where R′ is a C 1 -C 5 alkyl group.
11. The method of claim 7 , wherein the reaction is performed in a C 1 -C 20 alcohol solvent.
12. An organometallic complex prepared from the method of claim 7 .
13. An organic light emitting device, comprising:
a first electrode;
a second electrode; and
at least one organic layer between the first electrode and the second electrode, the at least one organic layer comprising an organic layer comprised of an organometallic complex represented by Formula 1:
where R 1 through R 16 are each independently selected from the group consisting of a hydrogen atom, a cyano group, a hydroxyl group, a nitro group, a halogen atom, a substituted or unsubstituted C 1 -C 20 alkyl group, a substituted or unsubstituted C 1 -C 20 alkoxy group, a substituted or unsubstituted C 6 -C 20 aryl group, a substituted or unsubstituted C 7 -C 20 arylalkyl group, a substituted or unsubstituted C 2 -C 20 alkylalkoxy group, a substituted or unsubstituted C 7 -C 20 arylalkoxy group, a substituted or unsubstituted C 6 -C 20 arylamino group, a substituted or unsubstituted C 1 -C 20 alkylamino group, a substituted or unsubstituted C 6 -C 20 heteroarylamino group, and a substituted or unsubstituted C 2 -C 20 hetero-ring group; and
M is a bivalent metal selected from the group consisting of Be, Mg, Zn, Ca, Cr, Fe, Co, Ni and Cu.
14. The organic light emitting device of claim 13 , wherein the organic layer comprised of the organometallic complex is an electron transport layer or an electron injection layer.
15. The organic light emitting device of claim 13 , wherein the organic layer comprised of the organometallic complex is an emitting layer.
16. The organic light emitting device of claim 13 , 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 emitting layer, a hole blocking layer, an electron transport layer and an electron injection layer.
17. The organic light emitting device of claim 16 , wherein said at least one organic layer comprises a hole injection layer, a hole transport layer, an emitting layer, optionally a hole blocking layer, an electron transport layer and an electron injection layer which are sequentially formed on the first electrode.
18. The organic light emitting device of claim 13 , wherein the organometallic complex is represented by one selected from the group consisting of Formulae 2 through 7:
where M is a bivalent metal selected from the group consisting of Be, Mg, Zn, Ca, Cr, Fe, Co, Ni and Cu; and
R 17 and R 18 are each independently selected from the group consisting of a hydrogen atom, a cyano group, a hydroxyl group, a nitro group, a halogen atom, a substituted or unsubstituted C 1 -C 20 alkyl group, a substituted or unsubstituted C 1 -C 20 alkoxy group, a substituted or unsubstituted C 6 -C 20 aryl group, a substituted or unsubstituted C 7 -C 20 arylalkyl group, a substituted or unsubstituted C 2 -C 20 alkylalkoxy group, a substituted or unsubstituted C 7 -C 20 arylalkoxy group, a substituted or unsubstituted C 6 -C 20 arylamino group, a substituted or unsubstituted C 1 -C 20 alkylamino group, a substituted or unsubstituted C 6 -C 20 heteroarylamino group, and a substituted or unsubstituted C 2 -C 20 hetero-ring group.
19. The organic light emitting device of claim 13 , wherein the organometallic complex is represented by one selected from the group consisting of Formulae 8 through 10: