Abstract

We have synthesized two functionalized prepolymers with an imide group meta to the propargylic function in their central skeleton. Based on data obtained by a variety of solid and liquid state physicochemical techniques, we show that meta substitution modifies the reaction path and leads to the formation of two chromenes, α and β. In addition, the reaction kinetics and thermal stability of the final system are affected by the presence of an imide group in the structure of the propargylic prepolymer.

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