Streamlined concept towards spatially resolved photoactivation of dynamic transesterification in vitrimeric polymers by applying thermally stable photolatent bases. Issue 9 (16th February 2022)

• Record Type: Journal Article
• Authors: Reisinger, David; Dietliker, Kurt; Sangermano, Marco; Schlögl, Sandra
• Is Part Of: Polymer chemistry. Volume 13:Issue 9(2022)
• Page Start: 1169
• Page End: 1176
• Publication Date: 2022-02-16
• Subjects: Polymers -- Periodicals; Macromolecules -- Periodicals; Polymerization -- Periodicals; 547.705
• DOI: 10.1039/d1py01722e
• Languages: English
• ISSNs: 1759-9954

Abstract

Abstract : Photolatent base catalysts exhibiting ideal structural properties for the straightforward manufacturing of thiol–epoxy vitrimers equipped with spatially resolved dynamic properties. Abstract : Through a well-targeted design, vitrimers are able to reorganise their three-dimensional covalently crosslinked network structure by associative exchange reactions when the so-called topology freezing transition temperature ( T v ) is exceeded. Although in the past decade a vast number of vitrimers have been developed, there is only a very limited number of elaborate strategies for enabling a controlled and spatially resolved onset of the exchange reactions above T v . Herein, we describe a convenient approach for a locally controllable photoactivation of vitrimeric properties in a covalently crosslinked thiol–epoxy network by the UV-mediated release of a strong amidine base acting as an efficient transesterification catalyst. In contrast to previous work, the applied photolatent catalysts benefit from superior solubility properties, adequate curing characteristics in the non-activated state (the addition of a supplementary catalyst is not required) and an excellent thermal stability. The spatially controlled activation of vitrimeric properties in terms of dynamic transesterification, macroscopically visible as a viscoelastic flow, is demonstrated by stress relaxation studies and a reshaping experiment. Moreover, we confirm that an undesired purely thermally induced catalyst release can be entirely excluded.