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Mendeleev Communications, 1998, Volume 8, Issue 2, Pages 43–44
DOI: https://doi.org/10.1070/MC1998v008n02ABEH000910
(Mi mendc4646)
 

This article is cited in 5 scientific papers (total in 5 papers)

Raman and UV-VIS study of the conformational polymorphism of solid tetramesityldisilene Mes2Si=SiMes2

L. A. Leitesa, S. S. Bukalova, J. E. Mangetteb, T. A. Schmedakeb, R. Westb

a Scientific and Technical Centre on Raman Spectroscopy, A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Moscow
b Department of Chemistry, University of Wisconsin, Madison, USA
Full-text PDF (208 kB) Citations (5)
Abstract: All three modifications of tetramesityldisilene 1 reported to date (orange unsolvated 1a and two yellow 1:1 solvates with toluene 1b and THF 1c) have been shown to readily transform to a new form, yellow unsolvated 1d, for which a quasi-trans conformation with two mesityl rings nearly orthogonal and the other two nearly coplanar to the double bond plane, is tentatively proposed. Form 1d appears to be the most stable conformational polymorph, but can be converted to the orange form upon illumination in the region 514–457 nm.
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Document Type: Article
Language: English


Citation: L. A. Leites, S. S. Bukalov, J. E. Mangette, T. A. Schmedake, R. West, “Raman and UV-VIS study of the conformational polymorphism of solid tetramesityldisilene Mes2Si=SiMes2”, Mendeleev Commun., 8:2 (1998), 43–44
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