Issue 23, 2019

Selective or living organopolymerization of a six-five bicyclic lactone to produce fully recyclable polyesters

Abstract

Organocatalyzed ring-opening polymerization (O-ROP) of a six-five bicyclic lactone, 4,5-trans-cyclohexyl-fused γ-butyrolactone (4,5-T6GBL), can be topologically selective or living at room temperature, depending on catalyst structure. A screening of (thio)urea [(T)U] and organic base pairs revealed unique trends in reactivity for this monomer as well as the most active catalyst pairs, which were employed as received commercially to produce relatively high molecular weight (Mn up to 106 kDa), low dispersity (Đ = 1.04) linear poly(4,5-T6GBL) in a living fashion. The ROP using a hybrid organic/inorganic pair of TU/KOMe in neat conditions led to poly(4,5-T6GBL) with even higher molecular weight (Mn = 215 kDa, Đ = 1.04). In comparison to the metal-catalyzed system, (T)U-base pairs exhibited competitive kinetics and reached higher monomer conversions, and their reactions can be performed in air. In addition, the resulting polymers required less purification to produce materials with higher onset decomposition temperature. (T)U-base pairs were selective towards linear polymerization only, whereas triazabicyclodecene can catalyze both polymerization and (quantitative) depolymerization processes, depending on reaction conditions. Cyclic polymers with Mn = 41–72 kDa were selectively formed via N-heterocyclic carbene-mediated zwitterionic O-ROP.

Graphical abstract: Selective or living organopolymerization of a six-five bicyclic lactone to produce fully recyclable polyesters

Supplementary files

Article information

Article type
Paper
Submitted
06 feb 2019
Accepted
27 mar 2019
First published
28 mar 2019

Polym. Chem., 2019,10, 3097-3106

Author version available

Selective or living organopolymerization of a six-five bicyclic lactone to produce fully recyclable polyesters

R. M. Cywar, J. Zhu and E. Y.-X. Chen, Polym. Chem., 2019, 10, 3097 DOI: 10.1039/C9PY00190E

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