Anthracene-containing binaphthol chromophores for light-emitting diode (LED) fabrication

被引:45
作者
Benmansour, H [1 ]
Shioya, T
Sato, Y
Bazan, GC
机构
[1] Univ Calif Santa Barbara, Dept Chem, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Dept Mat, Inst Polymers & Organ Solids, Mitsubishi Chem Ctr Adv Mat, Santa Barbara, CA 93106 USA
[3] Mitsubishi Chem Corp, MCC, Grp Sci & Technol Res Ctr, Aoba Ku, Yokohama, Kanagawa 2278502, Japan
关键词
D O I
10.1002/adfm.200304456
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Non-crystalline anthracene-containing binaphthol chromophores were synthesized, characterized, and used in the fabrication of organic light-emitting diodes (OLEDs). Specifically, the target molecules were 2,2'-dihexyloxy-1,1'-binaphthol-6,6'-bisanthracene (BA1) and 2,2'-dimethoxyy-1,1'-binaphthol-6,6'-bisanthracene (BA2). Molecules BA1 and BA2 provide amorphous solids, as determined by their glass-transition temperature (T-g) measured by differential scanning calorimetry (DSC). Efficient multilayer OLEDs containing BA1 and BA2 were fabricated by evaporation techniques. Differences in the electroluminescence frequencies of these devices suggests that the degree of alkoxide substitution controls the mobility within the binaphthol material, and therefore the recombination region in the device. Compound BA2 can also be used to dope CBP ((4,4'-bis(carbazol-9-)biphenyl)) in the fabrication of highly efficient OLEDs.
引用
收藏
页码:883 / 886
页数:4
相关论文
共 56 条
[31]   A NEW CATALYTIC-SYSTEM FOR AEROBIC OXIDATIVE COUPLING OF 2-NAPHTHOL DERIVATIVES BY THE USE OF CUCL-AMINE COMPLEX - A PRACTICAL SYNTHESIS OF BINAPHTHOL DERIVATIVES [J].
NOJI, M ;
NAKAJIMA, M ;
KOGA, K .
TETRAHEDRON LETTERS, 1994, 35 (43) :7983-7984
[32]  
Okumoto K, 2003, CHEM MATER, V15, P699, DOI [10.1021/cm020849+, 10.1021/cm020849]
[33]  
Ostrowski JC, 2001, CHEM-EUR J, V7, P4500, DOI 10.1002/1521-3765(20011015)7:20<4500::AID-CHEM4500>3.0.CO
[34]  
2-V
[35]   Chiral studies in amorphous solids: The effect of the polymeric glassy state on the racemization kinetics of bridged paddled binaphthyls [J].
Park, JW ;
Ediger, MD ;
Green, MM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (01) :49-56
[36]   1,1′-binaphthyl dimers, oligomers, and polymers: Molecular recognition, asymmetric catalysis, and new materials [J].
Pu, L .
CHEMICAL REVIEWS, 1998, 98 (07) :2405-2494
[37]  
Robinson MR, 2000, ADV MATER, V12, P1701, DOI 10.1002/1521-4095(200011)12:22<1701::AID-ADMA1701>3.0.CO
[38]  
2-U
[39]   Photophysics of phenylenevinylene polymers [J].
Rothberg, LJ ;
Yan, M ;
Papadimitrakopoulos, F ;
Galvin, ME ;
Kwock, EW ;
Miller, TM .
SYNTHETIC METALS, 1996, 80 (01) :41-58
[40]   Low molecular organic glasses for blue electroluminescence [J].
Salbeck, J ;
Yu, N ;
Bauer, J ;
Weissortel, F ;
Bestgen, H .
SYNTHETIC METALS, 1997, 91 (1-3) :209-215