Organic−Inorganic Hybrid Materials Incorporating Phosphorus-Containing Dendrimers

Phosphorus-containing dendrimers of first, second, and third generation with various peripheral functional groups and bearing a hydrolyzable Si(OEt) 3 group at the core have been prepared. Two synthetic routes were used: either the Si(OEt) 3 group was introduced from the start by reaction of (EtO) 3 Si(CH 2 ) 3 PPh 2 with an azide according to the Staudinger reaction ( A series of dendrimers) or the Si(OEt) 3 group was grafted to the core in the last step by reaction of 3-aminopropyltriethoxysilane with a vinyl group at the core ( B series of dendrimers). The silylated dendrimers were characterized by elemental analyses and 1 H, 13 C, 31 P, and 29 Si NMR spectroscopies. The cohydrolysis and polycondensation of these macromolecules with a defined and varying number of equivalents of tetraethoxysilane (TEOS) was carried out via sol−gel protocol, giving rise to dendrimer−silica xerogels. It was proven by 31 P NMR spectroscopy that the dendrimers were not damaged during the sol−gel process, and it was shown by 29 Si NMR spectroscopy that the dendrimer was covalently linked to the silica matrix by one Si−C bond. The texture of materials was determined by BET measurements. It was shown from elemental and thermogravimetric analysis that the percentage of incorporated organic part was notable but always inferior to the theoretical value.