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Quasilinear polyglycidols by triethyborane-controlled anionic polymerization of unprotected glycidol.

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In this study, quasilinear polyglycidols (PG)s with ultralow degree of branching (DB) could be synthesized through anionic polymerization of glycidol carried out in the presence of triethylborane (TEB). PGs with… Click to show full abstract

In this study, quasilinear polyglycidols (PG)s with ultralow degree of branching (DB) could be synthesized through anionic polymerization of glycidol carried out in the presence of triethylborane (TEB). PGs with DB ≤ 0.10, and molar masses up to 40 kg mol-1 could be indeed obtained using mono- or trifunctional ammonium carboxylates as initiator and under slow monomer addition conditions. The synthesis of degradable PGs through ester linkages obtained by copolymerization of glycidol with anhydride is also described. PG-based amphiphilic di- and triblock quasilinear copolymers were also derived. The role played by TEB is discussed and a polymerization mechanism is proposed.

Keywords: anionic polymerization; controlled anionic; quasilinear polyglycidols; triethyborane controlled; polyglycidols triethyborane; polymerization

Journal Title: Chemical communications
Year Published: 2023

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