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This article is cited in 10 scientific papers (total in 10 papers)
Electrochemistry of 1,1,2,2,3,3-hexa(2,6-diethylphenyl)cyclotristannane. The first examples of electrochemical generation of a stannylene radical anion and a tristannane radical cation
I. S. Orlova, A. A. Moiseevab, K. P. Butinb, L. R. Sitac, M. P. Egorova, O. M. Nefedova a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
c Department of Chemistry and Biochemistry, University of Maryland, Maryland, USA
Abstract:
The radical anion of di(2,6-diethylphenyl)stannylene (Ar2Sn) has been generated by the electrochemical reduction of cyclotristannane cyclo-(Ar2Sn)3, and the electrochemical oxidation of cyclo-(Ar2Sn)3 resulted in Sn–Sn bond cleavage with the formation of the radical cation of tristannane.
Citation:
I. S. Orlov, A. A. Moiseeva, K. P. Butin, L. R. Sita, M. P. Egorov, O. M. Nefedov, “Electrochemistry of 1,1,2,2,3,3-hexa(2,6-diethylphenyl)cyclotristannane. The first examples of electrochemical generation of a stannylene radical anion and a tristannane radical cation”, Mendeleev Commun., 12:4 (2002), 125–126
Linking options:
https://www.mathnet.ru/eng/mendc4125 https://www.mathnet.ru/eng/mendc/v12/i4/p125
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