Gels have been prepared via the sol-gel process by cohydrolysis of an
organoalkoxide of the type R(n)Si(OR')(4-n) and tetramethoxysilane. Th
e influence of organoalkoxide functionality and concentration on the r
esulting gel structure has been studied using two organoalkoxysilanes:
diphenyldimethoxysilane and phenyltrimethoxysilane. Phenyltrimethoxys
ilane-tetramethoxysilane and diphenyldimethoxysilane-tetramethoxysilan
e gels structures have been studied by solid-state NMR, small-angle X-
ray scattering, and differential scanning calorimetry. The interconnec
tion of the networks provided by the organoalkoxysilanes and tetrameth
oxysilane has been demonstrated. NMR and SAXS analysis showed that hyb
rid gels obtained with the trifunctional alkoxide are more condensed t
han the difunctional hybrid The scattering experiments demonstrate the
absence of any heterogeneities in the range 10-100 Angstrom. These ma
terials have a unique glass transition temperature that indicates the
existence of a homogeneous network.