1,2-DIMETHYL-1,2-DIPHENYLDISILANE-1,2-DIOL AND ITS K, NA, AND FE-II DERIVATIVES - MOLECULAR-STRUCTURE OF THE ALL-TRANS-ISOMER, TETRAPHENYL-1,4-DIOXA-2,3,5,6-TETRASILACYCLOHEXANE
Vv. Semenov et al., 1,2-DIMETHYL-1,2-DIPHENYLDISILANE-1,2-DIOL AND ITS K, NA, AND FE-II DERIVATIVES - MOLECULAR-STRUCTURE OF THE ALL-TRANS-ISOMER, TETRAPHENYL-1,4-DIOXA-2,3,5,6-TETRASILACYCLOHEXANE, Russian chemical bulletin, 45(10), 1996, pp. 2420-2426
Hydrolysis of 1,2-dimethyl-1,2-diphenyl-1,2-dichlorodisilane yields 1,
2-dimethyl-1,2-diphenyldisilane-1,2-diol, which undergoes dimerization
into stereoisomeric etraphenyl-1,4-dioxa-2,3,5,6-tetrasilacyclohexane
s under the action of H2SO4. Pure all-trans-isomer has been isolated a
nd characterized by H-1 NMR and IR spectroscopy and X-ray analysis. Th
e reaction of sodium disilanediolate with FeBr2 results in the formati
on of enyl-4-ferra(II)-3,5-dioxa-1,2-disilacyclopentane.