Publication Type : Journal Article
Thematic Areas : Advanced Materials and Green Technologies
Publisher : Indian Journal of Chemistry
Source : Indian Journal of Chemistry Section a-Inorganic Bio-Inorganic Physical Theoretical & Analytical Chemistry, Volume 40, p.986-988 (2001)
Campus : Coimbatore
School : School of Engineering
Center : Center for Excellence in Advanced Materials and Green Technologies
Department : Sciences, Chemistry, Civil
Year : 2001
Abstract : The reactions Of MeC6H4-SO2-SPh with organocobaloximes, RCo(dingH)(2)Py, (R = alkyl, benzyl, butenyl and allyl) under visible light photolysis show that the alkyl, butenyl and benzyl cobaloximes form the corresponding sulphides whereas the allyl cobaloximes form the organic sulphones.
Cite this Research Publication : B. Gupta, Oberoi, M., Mandal, D., Tiwari, U., Dr. Yamuna R., Vijaikanth, V., and Singh, V., “Homolytic displacements at carbon in organocobaloximes: Reactions of organocobaloximes with free radical precursor with two radical centres”, Indian Journal of Chemistry Section a-Inorganic Bio-Inorganic Physical Theoretical & Analytical Chemistry, vol. 40, pp. 986-988, 2001.