A new design strategy for organic optoelectronic materials by lateral boryl substitution

被引：216

作者：

Elbing, Mark ^{[1
,2
,3
]}

Bazan, Guillermo C. ^{[1
,2
,3
]}

机构：

[1] Univ Calif Santa Barbara, Dept Chem, Santa Barbara, CA 93106 USA

[2] Univ Calif Santa Barbara, Dept Biochem, Santa Barbara, CA 93106 USA

[3] Univ Calif Santa Barbara, Mat Ctr Polymers & Organ Solids, Santa Barbara, CA 93106 USA

来源：

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION | 2008年 / 47卷 / 05期

关键词：

boron; conjugation; fluorescence; molecular design; organic electronics;

D O I：

10.1002/anie.200703722

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

(Figure Presented) Lateral thinking: Molecular solids with tunable color and excellent emission efficiencies or increased electron affinities have been obtained by lateral boryl substitution on a π-delocalized framework (see picture, D = donor group, B = boryl group). This approach gives rise to a new design principle for organic optoelectronic materials. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.

引用

页码：834 / 838

页数：5

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