Synthesis of N, O π-conjugated boron complexes and the reactivity of Suzuki cross-coupling

被引:6
作者
Hu, Liangzhen [1 ]
Pan, Jing [1 ]
Zhang, Xiaohui [1 ]
Hu, Wen [1 ]
Xiong, Yan [1 ,2 ]
Zhu, Xiangming [3 ]
机构
[1] Chongqing Univ, Sch Chem & Chem Engn, Chongqing 400044, Peoples R China
[2] Nankai Univ, State Key Lab Elementoorgan Chem, Tianjin 300071, Peoples R China
[3] Univ Coll Dublin, Sch Chem & Chem Biol, Dublin 4, Ireland
基金
中国国家自然科学基金;
关键词
o-Hydroxy ketimine; BF3 center dot OEt2; pi-Conjugated boron complexes; Suzuki reaction; Biaryls; DIFLUORIDE DYES; LUMINESCENT PROPERTIES; HIGHLY FLUORESCENT; BORATE COMPLEXES; BODIPY DYES; ALCOHOLS; ETHERS; BENZYLATION; BF3-CENTER-DOT-OET2; DERIVATIVES;
D O I
10.1016/j.tet.2016.11.068
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
pi-Conjugated boron complexes have been considered as excellent fluorescent dye system and utilized in various fields, such as organic electronics, photonics, nanoemitters and dyestuff industry. In this paper, we developed a fluoroboron coordination by employing in situ generated BF3 center dot H2O as fluoroboron souce and afforded a series of novel species of N,O pi-conjugated boron complexes. Moreover, we achieved the Suzuki cross-coupling reaction of iodo-substituted complex with different boronic acids to further expand the structural diversity of N,O pi-conjugated fluoroboron complexes. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:223 / 229
页数:7
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