摘要:
The reaction of 1-(dimethylsilyl)-2-silylbenzene (4) and [{1,2-C6H4(SiMe2)(SiH2)}Pd(R2PCH2CH2PR2)] (6a, R = Me; 6b, R = Et) selectively afforded unique palladium complexes, depending on the phosphine ligands. For 6a, a dinuclear palladium complex with five Si-Si bonds was obtained, in which two 6a molecules were bridged by a cyclic dimer of 4 at the SiH2 silicon atom of 6a. On the other hand, 6b afforded a mononuclear palladium complex with a benzotrisilacyclopentene moiety, which was formed by two Si-Si coupling reactions between the SiH2 group of 6b and the SiH3 and SiMe2H groups of 4.