Nickel-Mediated Stepwise Transformation of CO to Acetaldehyde and Ethanol

被引:3
|
作者
Zhang, Ailing [1 ]
Raje, Sakthi [2 ]
Liu, Jianguo [1 ]
Li, Xiaoyan [1 ]
Angamuthu, Raja [2 ]
Tung, Chen-Ho [1 ]
Wang, Wenguang [1 ]
机构
[1] Shandong Univ, Sch Chem & Chem Engn, 27 South Shanda Rd, Jinan 250100, Shandong, Peoples R China
[2] Indian Inst Technol, Dept Chem, Lab Inorgan Synth & Bioinspired Catalysis LISBIC, Kanpur 208016, Uttar Pradesh, India
关键词
A SYNTHASE/CO DEHYDROGENASE; CARBON-MONOXIDE DEHYDROGENASE; METAL-CATALYZED CARBONYLATION; ACETYL-COENZYME; ACTIVE-SITE; ORGANOMETALLIC CHEMISTRY; BOND FORMATION; STRUCTURAL-CHARACTERIZATION; METHANOL CARBONYLATION; THIOESTER FORMATION;
D O I
10.1021/acs.organomet.7b00472
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The insertion of CO into the Ni-C bond of synthetic Ni(II)-CH3 cationic complex ([1-CH3](+)) affords a nickel-acetyl complex ([1-COCH3](+)). Reduction of resultant [1-COCH3](+) by borohydrides produces CH3CHO, CH3CH2OH, and an Ni(0) compound ([1](0)), which can react with CH3I to regenerate [1-CH3](+). By conducting deuterium labeling experiments, we have demonstrated that CH3CHO is the primary product from CH3CH2OH in such CO transformation reactions. In the reduction of [1-COCH3](+), the formation of CH3CHO competes with the loss of CH4, which leads to a Ni(0)-CO compound ([1-CO](0)) as a minor product. Our results establish fundamental steps in the exploration of nickel-mediated CO transformation to valuable chemicals.
引用
收藏
页码:3135 / 3141
页数:7
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