US2004142206A1PendingUtilityA1
Binaphthol based chromophores for the fabrication of blue organic light emitting diodes
Priority: Jan 17, 2003Filed: Jan 17, 2003Published: Jul 22, 2004
Est. expiryJan 17, 2023(expired)· nominal 20-yr term from priority
C07C 43/202C07D 401/10C07D 241/42C09K 2211/1044C09K 2211/1011C07D 321/10C09K 2211/1033C07D 217/24C07D 235/20C09K 11/06C07D 219/14C07D 209/86C07D 277/66C07D 263/57C07D 209/02C07D 223/26C07D 215/14C09K 2211/1048H05B 33/14C07D 471/04C07D 265/38C09K 2211/1029Y10S428/917C07D 321/12C07D 271/107H10K 85/621H10K 85/623H10K 85/622H10K 85/626H10K 85/654H10K 85/615H10K 85/311H10K 85/324H10K 85/40H10K 85/657H10K 85/6572H10K 2102/103H10K 85/649H10K 50/11
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Claims
Abstract
A blue electroluminescent material based on a binaphtyl compound of the general formula (I). Particular embodiments having the general formula have good solubilities in common organic solvents, resist crystallization and can be sublimed in a device fabrication process. These properties enable the fabrication of organic electroluminescent devices.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A binaphtyl compound of the formula:
wherein each Ar 1 and Ar 2 is independently a substituted or non-substituted aromatic hydrocarbon or a substituted or non-substituted aromatic heterocycle, each X 1 and x 2 is independently a substituted or non-substituted aromatic hydrocarbon, each n 1 and n 2 is independently 0 or 1, and wherein the compound's binaphtyl framework can be independently substituted at any position except those occupied by (X 1 )n 1 Ar 1 and (X 2 )n 2 Ar 2 .
2 . The binaphtyl compound of claim 1 wherein both Ar 1 and Ar 2 are three, four or five-condensed aromatic rings.
3 . The binaphtyl compound of claim 1 wherein both X 1 and X 2 are one, two or three-condensed aromatic rings.
4 . A binaphtyl compound of the formula:
wherein each Ar 1 and Ar 2 is independently a substituted or non-substituted aromatic hydrocarbon or a substituted or non-substituted aromatic heterocycle, each X 1 and X 2 is independently a substituted or non-substituted aromatic hydrocarbon, each n 1 and n 2 is independently 0 or 1, each R 1 and R 2 is independently a hydroxyl group, a substituted or non-substituted alkyl group, or a substituted or non-substituted alkoxy group, wherein R 1 and R 2 can be bound to each other to form a ring structure wherein the ring structure can have substituent groups, and wherein the compound's binaphtyl framework can be independently substituted by a halogen, a hydroxyl group, or a substituted or non-substituted alkyl, alkenyl, alkoxy or alkoxycarbonyl group at any position except those occupied by (X 1 )n 1 Ar 1 , (X 2 )n 2 Ar 2 , R 1 and R 2 .
5 . The binaphtyl compound of claim 4 wherein each R 1 and R 2 is an alkoxy group.
6 . A fluorescent dye of the binaphtyl compound of claim 1 .
7 . An organic light emitting device having an anode and cathode and an emissive layer between the anode and cathode, and including a layer comprising the binaphtyl compound of claim 1 .
8 . An organic light emitting device having an anode and cathode and an emissive layer between the anode and cathode, the emmisive layer comprising the binaphtyl compound of claim 1 .
9 . The device of claim 8 wherein the concentration of the binaphtyl compound is between 0.01 to 20% by weight.
10 . An organic light emitting device comprising an anode and a cathode, and an emissive layer between the anode and cathode, the device including a layer between the emissive layer and the cathode comprising the binaphtyl compound of claim 1 .
11 . An organic light emitting device comprising an anode and a cathode, and an emissive layer between the anode and cathode, the device including a layer between the anode and the emissive layer comprising the binaphtyl compound of claim 1.Join the waitlist — get patent alerts
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