Abstract
A series of cyclopalladated carbosilane dendrimers functionalized with monoanionic [C6H4(CH2NMe2)-4]- (= CN) C,N-chelating ligands via a multiple and selective C-H bond activation process have been prepared. The structure of the support, i.e., the branching degree as well as the nature of the alkanediyl linkers present in the carbosilane dendrimer, was
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