Cobalt-catalyzed dehydrative approach for the synthesis of unsymmetric disiloxanes and polysiloxanes

被引:2
|
作者
Yang, Bing-Bin [1 ]
Guo, Peng [1 ]
He, Xinglei [1 ]
Ye, Ke-Yin [1 ]
机构
[1] Fuzhou Univ, Fujian Prov Univ, Coll Chem, Key Lab Mol Synth & Funct Discovery, Fuzhou 350108, Peoples R China
来源
ORGANIC CHEMISTRY FRONTIERS | 2024年 / 11卷 / 15期
基金
中国国家自然科学基金;
关键词
DOUBLE-BONDS; SILICON; SILOXANES; ACTIVATION; SILANOLS; HYDROGEN; ESTERS; PHASE;
D O I
10.1039/d4qo00706a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Conventional approaches to unsymmetric disiloxanes involve the condensation of silanol with hydroxy-, chloro-, or alkoxysilanes, which suffers from several limitations such as limited substrate scope, the requisite use of stoichiometric bases, expensive transition-metal catalysts, and typically unsatisfactory product selectivity. Herein, we report a dehydrative cobalt catalysis for unsymmetric disiloxane from two different silanols, which features a low loading of the earth-abundant cobalt catalyst, easy operation, good functional combinability, and gram-scale preparation. Notably, this approach also enables the facile preparation of unsymmetric polysiloxanes. A highly selective and scalable dehydrative approach for the synthesis of unsymmetric disiloxanes and polysiloxanes is reported using Earth-abundant cobalt catalyst under an air atmosphere.
引用
收藏
页码:4125 / 4130
页数:6
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