A hybrid xerogel of 1,4-bis(trimethoxysilylethynyl)benzene was prepared by
using a sol-gel process. Chemical treatment of this material was performed
under mild conditions in order to remove the organic group using fluoride a
nion as a catalyst. Experimental procedures were carried out using differen
t solvents, acidities and counter-cations in order to modify the nucleophil
ic power of F-. Characterization of the residues was done by elemental anal
ysis, spectroscopy (Si-29 NMR), thermal analysis, pycnometry, surface area
measurement and SAXS. The efficiency of the chemical treatment is related t
o the solvation of the F- anion. It was possible to demonstrate that elimin
ation of the organic part occurs at the same time as a reorganization of th
e silica network. This reorganization is the result of two competitive F--c
atalyzed chemical reactions: a redistribution and a polycondensation proces
s known in solution and which take place in the solid. These processes acco
unt for the textural characteristics of the final material and may efface t
he organization of the organic spacers in the hybrid xerogel. These results
demonstrate the limitations of silica as a molecular imprinting material a
nd open a new approach to porous silica with adjustable pore size.