A versatile scaffold for facile synthesis of fluorescent cyano-substituted stilbenes

被引：10

作者：

Hayashi, Shotaro ^{[1
]}

Sakamoto, Minami ^{[2
]}

Ishiwari, Fumitaka ^{[2
]}

Fukushima, Takanori ^{[2
]}

Yamamoto, Shin-ichi ^{[1
]}

Koizumi, Toshio ^{[1
]}

机构：

[1] Natl Def Acad, Dept Appl Chem, 1-10-20 Hashirimizu, Yokosuka, Kanagawa 2398686, Japan

[2] Tokyo Inst Technol, Inst Innovat Res, Lab Chem & Life Sci, Midori Ku, 4259 Nagatsuta, Yokohama, Kanagawa 2268503, Japan

来源：

TETRAHEDRON | 2019年 / 75卷 / 08期

基金：

日本学术振兴会;

关键词：

pi-Conjugated molecule; Fluorescence; Scaffold; WITTIG OLEFINATION REACTION; CONJUGATED POLYMER-FILMS; CROSS-COUPLING REACTIONS; CARBON BOND FORMATION; ENHANCED EMISSION; PALLADIUM; DERIVATIVES; ARYLATION; CATALYSIS; CRYSTALS;

D O I：

10.1016/j.tet.2019.01.012

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Here we report the facile derivatization of a cyano-substituted stilbene into higher pi-extended analogues. The cyano-substituted stilbene, which serves as a synthetic scaffold, has a bromo group and a formyl group on its 4- and 4'-position of the phenylene rings and thus readily undergoes selective transformation into other functional groups using various simple organic reactions. The resultant pi-conjugated molecules that contain a cyano-substituted stilbene skeleton exhibit fluorescence in solution and in the solid state. (C) 2019 Elsevier Ltd. All rights reserved.

引用

页码：1079 / 1084

页数：6

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