Dendrimers and arborols with a carbosilane core have been prepared by
a divergent hydrosilylation/vinylation reaction sequence followed by m
ethoxylation of the silicon chloride end groups. Dendrimers with respe
ctively 12 [first generation (1G)] and 36 [second generation (2G)] met
hoxysilane groups and arborols with octadecyl and phenyl group of firs
t and second generation have been prepared. They were characterized by
elemental analyses and H-1, C-13 and Si-29 NMR spectroscopy. Polycond
ensation by a sol-gel process yields the hybrid materials. 2G; dendrim
ers formed porous materials while nonporous materials were obtained fr
om 2G arborols containing the octadecyl group. The precursor of the se
cond generation containing the phenyl group formed different gels depe
nding on the solvent used for the polycondensation process. Neverthele
ss, no gel was obtained for dendrimers and arborols of the first gener
ation. The solid-state 29Si NMR spectroscopy was used to evaluate the
integrity of the material and to determine the degree of polycondensat
ion in the network material. Oxidative thermal treatment was performed
in order to remove the organic part of the hybrids. The texture of th
e solid was determined by BET measurement for xerogel before and after
oxidation. Porous silica were obtained with similar porosity and pore
size diameter from all the precursors.