Abstract

Hybrid organic–inorganic sol–gel compounds have been widely used for the design of new optical devices, since they combine the characteristics of both glasses and polymers and improve the properties of the final material. Hybrid precursors in which both phases are chemically grafted are of increasing interest: volume shrinkage is minimized and phase separation can be kept below the level of Rayleigh scattering, thus leading to highly transparent glasses. Polymerizable acrylate or methacrylate functions grafted onto modified silicone alkoxides can react ia a free-radical mechanism initiated either by heating or UV-light. Considerable attention has already been focused on the chemical mechanisms involved in the construction of the inorganic network. However, no extensive study of the organic part of the process has so far been conducted. This paper points out the characteristics of the photopolymerization process taking place in hybrid sol–gel materials. In particular, the influence of inorganic moieties on the photopolymerization kinetics was studied by UV and real time FTIR spectroscopy. Particular interest was focused on the incorporation of alkoxymetals that are usually added to improve the optical and physical properties of the final material. The role of the titanium component in the photopolymerization process is emphasized. The results provide insights into processes leading to simultaneous formation of interpenetrating organic–inorganic networks and are of crucial importance for the generation of optical devices.

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