Abstract
We report herein the synthesis, the functionalization, and the successful radical polymerization of very nonlinear optical (NLO) active push–pull polyene chromophores (CPO). Second, the thermal Huisgen cyclo-addition cross-linking reaction was implemented, and it proved to be fully compatible with a polyene-based push–pull chromophore. Toward this goal, PMMA-co-CPO-3 and two cross-linkable polymers (PCC1-CPO-3 and PCC2-CPO-3) were first prepared and characterized by a modified Teng and Man technique performed in transmission. These first series of polymers were not compatible with the applied poling conditions because an irreversible film degradation was systematically observed at a temperature significantly lower than the cross-linking temperature. Consequently, a second series of polymers was prepared, in which the cross-linking temperature was decreased by functionalizing acetylenic moieties with ester electron withdrawing groups, which decrease the activation energy of the thermal Huisgen cyclo-addition. These new polymers were stable until the cross-linking reaction, and they exhibit bulk electro-optic coefficients (r33) until 41 pm/V at 1.5 μm. Furthermore, it was shown that the Huisgen cross-linking reaction is compatible with such push–pull polyene-based chromophores, and it systematically enhances the stability of the electro-optic activity because chromophore orientation was maintained up to 96 °C against 70 °C for the same uncross-linked polymer.
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