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A simple isocyanate-free method to synthesize poly(trimethylene carbonate hydroxy-urethane)s is described. The strategy first involves the synthesis of α,ω-di(cyclic carbonate) telechelic polycarbonate precursors upon ring-opening polymerization of trimethylenecarbonate using a cyclic carbonate alcohol as chain transfer agent, followed by the ring-opening polyaddition of the terminal cyclic carbonate with a diamine. Such poly(carbonate-hydroxyurethane)s exhibit macromolecular carbonate segments of tunable length/molar mass.
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