Abstract
Catalytic intramolecular cyclization of 3-aminopropylalkoxysilanes and 3-aminopropylalkoxydisiloxanes in the presence of hexamethyldisilazane has been studied; structure and reactivity of the formed azasilacyclopentanes have been investigated. In particular, the prepared cyclic azasilanes were studied by 1H, 29Si, and 13C NMR spectroscopy. Possibility of catalytic co-condensation of the compounds containing methoxy and trimethylsiloxy groups with preservation of azasilacyclopentane structure has been demonstrated. Depending on temperature and the reactants ratio, the interaction of 3-aminopropylmethyldimethoxysilane with hexamethyldisilazane can yield 1-(trimethylsilyl)-2-methyl-2-methoxy-1-aza-2-silacyclopentane or the polymer bearing azasilacyclopentane fragments in the main chain.
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Original Russian Text © T.R. Salikhov, V.M. Kopylov, D.I. Shragin, 2014, published in Zhurnal Obshchei Khimii, 2014, Vol. 84, No. 5, pp. 782–788.
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Salikhov, T.R., Kopylov, V.M. & Shragin, D.I. Silylated derivatives of azasilacyclopentanes. Russ J Gen Chem 84, 875–882 (2014). https://doi.org/10.1134/S1070363214050168
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DOI: https://doi.org/10.1134/S1070363214050168