Synthesis of various boron-containing disilanes |
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Authors: | C Lehnert K Trommer G Roewer |
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Institution: | (1) TU Bergakademie Freiberg, Institute of Inorganic Chemistry, Leipziger Straße 29, D-09596 Freiberg, Germany |
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Abstract: | The stepwise reaction of the Si-Cl functions of 1,1,2,2-tetrachlorodimethyldisilane with RMgBr using the diethylamino unit as protecting group enables the synthesis of disilanes Si2Me2RxCl4–x, bearing one to four olefinic substituents (R = vinyl, -allyl and ethynyl). The catalyst free hydroboration of such molecules represents a convenient way to prepare boron containing chlorodisilanes. 9-BBN exhibits a very high regioselectivity in the hydroboration of vinyl-, allyl-or ethynyldisilanes. In case of the ethynyl group, the hydroboration of 1,1,2-trichloro-2-ethynyldimethyldisilane and 1,2-dichloro-1,2-diethynyldimethyldisilane by the twofold addition of the 9-BBN in two separate steps was confirmed by NMR spectroscopy. |
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Keywords: | 9-borabicyclo[3 3 1]nonane disilanes hydroboration NMR multinuclear |
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