Please use this identifier to cite or link to this item: https://doi.org/10.1021/om1005947
Title: CpMn(CO)3-catalyzed photoconversion of thiols into disulfides and dihydrogen
Authors: Tan, K.Y.D.
Kee, J.W.
Fan, W.Y. 
Issue Date: 25-Oct-2010
Citation: Tan, K.Y.D., Kee, J.W., Fan, W.Y. (2010-10-25). CpMn(CO)3-catalyzed photoconversion of thiols into disulfides and dihydrogen. Organometallics 29 (20) : 4459-4463. ScholarBank@NUS Repository. https://doi.org/10.1021/om1005947
Abstract: The UV photolysis of CpMn(CO)3 with thiols at room temperature effected the following catalytic transformation: 2 RSH → R 2S2 + 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. © 2010 American Chemical Society.
Source Title: Organometallics
URI: http://scholarbank.nus.edu.sg/handle/10635/93408
ISSN: 02767333
DOI: 10.1021/om1005947
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