Regioselective Ring-Opening of Terminal Epoxides Catalyzed by a Porous Metal Silicate Material

被引:0
|
作者
Liu, Yang-Yang [1 ]
Wu, Chuan-De [1 ]
机构
[1] Zhejiang Univ, Dept Chem, State Key Lab Silicon & Adv Semicond Mat, Hangzhou 310027, Peoples R China
基金
中国国家自然科学基金;
关键词
CHEMOSELECTIVE HYDROGENOLYSIS; BIOTECHNOLOGICAL PRODUCTION; STYRENE OXIDE; 2-PHENYLETHANOL; HYDROGENATION; CONVERSION; ALCOHOLS; NANOPARTICLES;
D O I
10.1021/acs.inorgchem.3c03554
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Reductive ring-opening of epoxides is a green pathway for synthesizing highly value-added alcohols. In this study, we present a practically applicable approach for the synthesis of anti-Markovnikov-type alcohols with high yields from aliphatic and aromatic epoxides under mild conditions by developing porous metal silicate (PMS) catalysts. A PMS material PMS-20 consists of cobalt and nickel bimetal redox-active sites, exhibiting exceptional catalytic activity and selectivity in the reductive ring-opening of terminal epoxides with >99% yield of primary alcohols. Comparing with the existing methods using noble metals, PMS-20 exhibits broad substrate scope and excellent functional group tolerance by synergistic work between cobalt and nickel species, which is clarified by dual chamber cell system characterization and theoretical calculation results.
引用
收藏
页码:1166 / 1174
页数:9
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