
Phosphorus, Sulfur and Silicon and the Related Elements p. 9 - 14 (2001)
Update date:2022-08-29
Topics:
Purkayastha
Baruah
Phenylsilane and diphenylsilane undergoes rearrangement reactions by palladium catalysts such as Pd(TMEDA)Cl2, Pd(TEEDA)Cl2, [Pd(PPh3)]2Cl2 (where TMEDA = tetramethylethylenediamine, TEEDA = tetraethylethylenediamine) at room temperature. However, the reductive Si-O bond forming reaction can be performed on hydrosilanes through competitive paths. The reactions of phenylsilane and quinonic compounds are catlaysed by Pd(TMEDA)Cl2 (such as 1,4-benzoquinone, 1,4-napthoquinone) to give siloxanes, backbone of these siloxanes which contains rearranged phenylsilane units. The thin films of such oligomers has plot of resistance vs temperature profile resembling semiconductor.
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