IP Library Granted Patent US 6,921,591
Granted Patent B2
US 6,921,591 · App. 10/686,663 · Granted Jul 26, 2005

Luminescent device material, luminescent device using the same, and amine compound

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Quick Facts
Patent No.
US 6,921,591
App. No.
10/686,663
Granted
Jul 26, 2005
Kind
B2
Abstract

An organic luminescent device material, comprising an amine compound represented by the following formula (I): wherein R 1 , R 2 and R 3 , which are the same or different, each represents an unsubstituted or substituted aryl group, an unsubstituted or substituted heterocyclic group or an unsubstituted or substituted aliphatic hydrocarbon group, provided that at least two among R 1 , R 2 and R 3 are each an unsubstituted or substituted aryl or heterocyclic group; or any two among R 1 , R 2 and R 3 combine with each other to complete a ring; provided that at least one among R 1 , R 2 and R 3 has a moiety represented by the following formula (II), wherein R 4 , R 5 and R 6 each represents a hydrogen atom or a substituent group, Z 1 represents atoms forming a 5, 6 or 7-membered ring, and m represents 0, 1 or 2.

Claims (20)

1. A luminescent device comprising at least one organic layer between electrodes, said at least one organic layer comprising at least one compound represented by formula (XIII):

wherein Ar 41 represents an arylene group or a divalent heterocyclic group; R 42 represents an aryl group, a heterocyclic group or an aliphatic hydrocarbon group; R 44 , R 45 and R 46 each represent a hydrogen atom or a substitutent group; Z 4 represents atoms forming a 5, 6 or 7-membered ring; m represents 0, 1 or 2; p represents 2 or 3, and two or three combinations made with Ar 41 , R 42 , R 44 , R 45 , R 46 , Z 4 and m are the same or different.

2. The luminescent device of claim 1 , wherein the compound of formula (XIII) is a compound represented by the following formula (XV):

wherein R 62 represents an aryl group, a heterocyclic group or an aliphatic hydrocarbon group; R 64 , R 65 and R 66 each represent a hydrogen atom or a substituent group; R 67 represents a substituent group; q represents an integer of 0 to 4, and when q is 2, 3 or 4 the R 67 groups are the same or different; Z 6 represents atoms forming a 5, 6 or 7-membered ring; m represents 0, 1 or 2; p represents 2 or 3, and two or three combinations made with R 62 , R 64 , R 65 , R 66 , R 67 , Z 6 , m and q are the same as or different from one another.

3. A luminescent device comprising at least one organic layer between electrodes, said at least one organic layer comprising at least one compound represented by formula (XVII):

wherein R 84 represents a hydrogen atom or a substituent group; R 87 and R 88 each represent a substituent group; q represents an integer of 0 to 4, and when q is 2, 3 or 4 the R 87 groups are the same or different; r represents an integer of 0 to 5, and when r is 2, 3, 4 or 5 the R 88 groups are the same or different; Z 8 represents atoms forming a 5, 6 or 7-membered ring; X 8 represents an oxygen atom, a sulfur atom, N—R A1 or CR A2 R A3 ; R A1 , R A2 and R A3 each represent a hydrogen atom or a substituent group; t represents an integer of at least 2, and one combination made with R 84 , R 87 , R 88 , Z 8 , X 8 , q and r is the same as or different from another combination made therewith; and L represents a t-valent linkage group.

4. The luminescent device of claim 3 , wherein Z 8 represents 1,3-indanedione nucleus, a pyrazolone nucleus, an isooxazolinone nucleus, an oxaolinone nucleus, a furanone nucleus, an oxyindole nucleus, a 1-indanone nucleus, an imidazolidone nucleus, a benzothiophene-3-one nucleus, an oxobenzothiophene-3-one nucleus, a dioxobenzothiophene-3-one nucleus, a coumaranone nucleus, a 2-thio-2,4-thiazolidinedione nucleus, a 2-thio-2,4-oxazolidinedione nucleus, a 2-thio-2,5-thiazolidinedione nucleus or a 2,4-thiazolidinedione nucleus.

5. The luminescent device of claim 4 , wherein Z 8 represents 1,3-indanedione nucleus, a dioxobenzothiophene-3-one nucleus, a coumaranone nucleus, a 2-thio-2,4-thiazolidinedione nucleus, a 2-thio-2,4-oxazolidinedione nucleus, a 2-thio-2,5-thiazolidinedione nucleus or a 2,4-thiazolidinedione nucleus.

6. The luminescent device of claim 5 , wherein L represents phenylene, biphenylene or triphenylene.

7. The luminescent device of claim 5 , wherein t represents 2 or 3.

8. The luminescent device of claim 3 , wherein L represents phenylene, biphenylene or triphenylene.

9. The luminescent device of claim 3 , wherein t represents 2 or 3.

10. A styrylamine compound comprising a structure represented by formula (XVIII):

wherein R 94 represents a hydrogen atom or a substituent group; R 97 and R 98 each represent a substituent group; q represents an integer of 0 to 4, and when q is 2, 3 or 4 the R 97 groups are the same or different; r represents an integer of 0 to 5, and when r is 2, 3, 4 or 5 the R 98 groups are the same or different; Z 9 represents atoms forming a 5, 6 or 7-membered ring; X 9 represents an oxygen atom, a sulfur atom, N—R A1 or CR A2 R A3 ; R A1 , R A2 and R A3 each represent a hydrogen atom or a substituent group; t represents an integer of at least 2, and one combination made with R 94 , R 97 , R 98 , Z 9 , X 9 , q and r is the same as or different from another combination made therewith; and L represents a t-valent linkage group.

11. The styrylamine compound of claim 10 , wherein Z 9 represents 1,3-indanedione nucleus, a pyrazolone nucleus, an isooxazolinone nucleus, an oxazolinone nucleus, a furanone nucleus, an oxyindole nucleus, a 1-indanone nucleus, an imidazolidone nucleus, a benzothiophene-3-one nucleus, an oxobenzothiophene-3-one nucleus, a dioxobenzothiophene-3-one nucleus, a coumaranone nucleus, a 2-thio-2,4-thiazolidinedione nucleus, a 2-thio-2,4-oxazolidinedione nucleus, a 2-thio-2,5-thiazolidinedione nucleus or a 2,4-thiazolidinedione nucleus.

12. The styrylamine compound of claim 11 , wherein Z 9 represents 1,3-indanedione nucleus, a dioxobenzotbiophene-3-one nucleus, a coumaranone nucleus, a 2-thio-2,4-thiazolidinedione nucleus, a 2-thio-2,4-oxazolidinedione nucleus, a 2-thio-2,5-thiazolidinedione nucleus or a 2,4-thiazolidinedione nucleus.

13. The styrylamine compound of claim 12 , wherein L represents phenylene, biphenylene or triphenylene.

14. The styrylamine compound of claim 12 , wherein t represents 2 or 3.

15. The styrylamine compound of claim 10 , wherein L represents phenylene, biphenylene or triphenylene.

16. The styrylamine compound of claim 10 , wherein t represents 2 or 3.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 1, 2012
From: FUJIFILM CORPORATION
To: UDC IRELAND LIMITED
Reel/Frame 028889/0636 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 15, 2007
From: FUJIFILM HOLDINGS CORPORATION (FORMERLY FUJI PHOTO FILM CO., LTD.)
To: FUJIFILM CORPORATION
Reel/Frame 018904/0001 →