| Literature DB >> 31241821 |
Juliette Brunet1, Franck Collas2, Matthieu Humbert1, Lionel Perrin3, Fabrice Brunel1, Emmanuel Lacôte4, Damien Montarnal1, Jean Raynaud1.
Abstract
Differential scanning calorimetry of high molar mass poly(4-vinylphenylboronic acid, pinacol ester)s evidenced unusual reactive events above 120 °C, resulting in a high glass-transition temperature of 220 °C. A reversible ring-opening reactivity of pinacol boronates is proposed, involving a nucleophilic attack on the sp2 boron and subsequent bridging between boron atoms by interconnected pinacol moieties to form a densely crosslinked network with high Tg . FTIR, solid-state NMR investigations, and rheology studies on the polymer as well as double-tagging analyses on molecular model structures and theoretical calculations further support this hypothesis and indicate a ring-opening inducing crosslinking. When diluted in an apolar solvent such as toluene, the polymer network can be resolubilized via ring closing, thus recovering the entropically favored linear chains featuring cyclic boronate esters.Entities:
Keywords: boron chemistry; dynamic networks; high glass-transition temperature; organoboron polymers; reversible crosslinking
Year: 2019 PMID: 31241821 DOI: 10.1002/anie.201904559
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336