Synthesis of 1,3-bis(silyl/germyl)propanes by hydrosilylation of allylgermanes in the presence of Karstedt catalyst

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Resumo

The hydrosilylation reactions of allylgermanes R3GeAll (R = Cl, Me) in the presence of Karstedt catalyst with a number of phenyl- and thienyl-containing hydridosilanes were studied. It was found that the efficiency of the studied reactions is determined by a combination of several factors: the nature of the substituents at the germanium atoms in the initial olefins; the degree of hydridity of the hydrogen atoms in the initial hydridosilanes; the electronic and steric properties of the substituents at the silicon atoms of the hydridosilanes and their tendency to redistribution of deputies at silicon and germanium atoms. The synthesized compounds were identified using NMR 1H and 13C spectroscopy.

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Sobre autores

V. Lakhtin

State Research Institute of Chemistry and Technology of Organoelement Compounds

Autor responsável pela correspondência
Email: vlachtin@rambler.ru
Rússia, Moscow, 105118

D. Efimenko

State Research Institute of Chemistry and Technology of Organoelement Compounds

Email: vlachtin@rambler.ru
Rússia, Moscow, 105118

A. Shestakova

State Research Institute of Chemistry and Technology of Organoelement Compounds

Email: vlachtin@rambler.ru
Rússia, Moscow, 105118

I. Sokolskaya

State Research Institute of Chemistry and Technology of Organoelement Compounds

Email: vlachtin@rambler.ru
Rússia, Moscow, 105118

N. Kirilina

State Research Institute of Chemistry and Technology of Organoelement Compounds

Email: vlachtin@rambler.ru
Rússia, Moscow, 105118

P. Storozhenko

State Research Institute of Chemistry and Technology of Organoelement Compounds

Email: vlachtin@rambler.ru
Rússia, Moscow, 105118

Bibliografia

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