posted on 2019-03-04, 12:52authored byMaria M. Heffernan, Emmet J. O'Reilly
As part of ongoing efforts to develop electroactive polymers (EAPs) which are biodegradable/bioresorbable, we report on the microwave assisted synthesis and characterization of an electrically conducting and electroactive polymer that capitalises on pKa sensitivity to initiate the system’s fracture and breakdown. The system, poly(bis((thiophen-2-yl) methylene) benzene-1,4-diamine), a poly(thiophene-azomethine) co-polymer (PAZO), incorporates hydrolytically sensitive azomethine linkers amongst bithiophene units resulting in one continuously conjugated and redox-active macromolecular framework. Rapid microwave assisted synthesis allowed for facile preparation of the polymer with significantly reduced reaction times when compared to traditional synthetic routes. Electrochemical analysis indicated quasi-reversible electrochemical behaviour with sufficiently high conductivity for in vivo biomedical applications. The polymer displays tunable degradation behaviour whereby the time duration required for polymeric breakdown is a function of the pKa of the acid used to catalyse the reaction resulting in controllable degradation times ranging from 1 h to 6 months. The development of conductive polymeric materials that are fully degradable over pre-defined time periods opens up a portal to the next generation of EAPs for in vivo biomedical applications.
History
Publication
European Polymer Journal;114, pp. 206-212
Publisher
Elsevier
Note
peer-reviewed
Rights
This is the author’s version of a work that was accepted for publication in European Polymer Journal. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in European Polymer Journal, 2019, 114, pp. 206-212, https://doi.org/10.1016/j.eurpolymj.2019.02.005