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Part of the book series: Advances in Silicon Science ((ADSS,volume 2))

The concept of highly symmetrical, perfectly branched macromolecules prepared in a generational fashion was introduced in 1978 [1]. The synthesis of polylysine dendrimers [2] and the seminal research by Tomalia and Newkome in the mid-1980s established that such molecules could indeed be prepared [3, 4]. Tomalia et al. used trifunctional nitrogen branch points and Newkome chose tetrafunctional carbon branch points. These dendrimers contained ether, ester, amine and amide polar bonds

Carbosilane dendrimers with a silicon branch point in an exclusively carbon–silicon skeleton are non-polar, inert, neutral and thermally and hydrolytically stable compounds. The absence of polar bonds facilitates the use of many derivatization reactions and creates the possibility of strong physico-chemical contrast between the core and the outer corona. The synthesis of carbosilane dendrimers is almost always by a divergent process from the core to the interior generations and to the periphery, with the number of reactions per dendrimer increasing geometrically with each generation (see Chapter 1). The divergent synthesis of carbosilane dendrimers consists of the generational repetition of a sequence of two clean, high-yield reactions: (a) hydrosilylation and (b) nucleophilic substitution by Grignard or organolithium reagents. The hydrosilylation reaction 3.1 introduces the branch juncture and creates the next generation

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Roovers, J., Ding, J. (2009). Carbosilane Dendrimers. In: Dvornic, P.R., Owen, M.J. (eds) Silicon-Containing Dendritic Polymers. Advances in Silicon Science, vol 2. Springer, Dordrecht. https://doi.org/10.1007/978-1-4020-8174-3_3

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