Synthesis of π-conjugated, pyridine ring functionalized bis-terpyridines with efficient green, blue, and purple emission

被引:33
作者
Han, Fu-She [1 ]
Higuchi, Masayoshi [1 ]
Kurth, Dirk G. [1 ,2 ]
机构
[1] Natl Inst Mat Sci, Organ Nanomat Ctr, Funct Modules Grp, Tsukuba, Ibaraki 3050044, Japan
[2] Max Planck Inst Colloids & Interfaces, D-14424 Potsdam, Germany
关键词
synthesis; terpyridine; Suzuki coupling; light-emission; supramolecule; polymer; functional materials;
D O I
10.1016/j.tet.2008.06.106
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A large variety of rigid, pi-conjugated, pyridine ring functionalized bis-terpyridines are synthesized efficiently using tandem Miyaura/Suzuki-type cross-coupling reaction. Photophysical property study reveals that the absorption and luminescent properties of the obtained bis-terpyridines are profoundly affected by the nature of the functional groups at the peripheral pyridine and the spacers. Namely, by tailoring precisely the Structures, the light-emitting efficiencies of bis-terpyridines can be enhanced significantly with quantum yields (phi(f)) of up to 0.62, and the emission colors can be tuned to display distinct colors including purple, bright blue, and bright green. Consequently, the novel bis-terpyridines are attractive ligands for the assembly of new metallo-supramolecule based functional materials. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:9108 / 9116
页数:9
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