化学
催化作用
锰
环戊二烯
光化学
化学选择性
傅里叶变换红外光谱
光解
反应机理
有机化学
化学工程
工程类
作者
Kheng Yee Desmond Tan,Jun Wei Kee,Wai Yip Fan
出处
期刊:Organometallics
[American Chemical Society]
日期:2010-09-07
卷期号:29 (20): 4459-4463
被引量:33
摘要
The UV photolysis of CpMn(CO)3 with thiols at room temperature effected the following catalytic transformation: 2 RSH → R2S2 + H2. This reaction is a cleaner and greener way toward making disulfides, as it produces dihydrogen as the only side-product. The manganese system exhibits high chemoselectivity as the transformation proceeds efficiently even in the presence of numerous functional groups. A manganese dicarbonyl complex, CpMn(CO)2RSH, and cyclopentadiene have also been detected using FTIR and NMR spectroscopic techniques, respectively. Based on our experimental data, a mechanism has been proposed to account for the catalysis.
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