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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.
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页码:1166 / 1174
页数:9
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