Click to Self-immolation: A "Click" Functionalization Strategy towards Triggerable Self-Immolative Homopolymers and Block Copolymers

  • Angew Chem Int Ed Engl. 2024 Jan 15;63(3):e202317063. doi: 10.1002/anie.202317063.
Zhengyu Deng  1 Xiaoli Liang  1 Elizabeth R Gillies  1  2
Affiliations
  • 1. Department of Chemistry, The University of Western Ontario, London, Ontario, N6A 5B7, Canada.
  • 2. Department of Chemical and Biochemical Engineering, The University of Western Ontario, London, Ontario, N6A 5B9, Canada.
Abstract

Self-immolative Polymers (SIPs) are a class of degradable macromolecules that undergo stimuli-triggered head-to-tail depolymerization. However, a general approach to readily end-functionalize SIP precursors for programmed degradation remains elusive, restricting access to complex, functional SIP-based Materials. Here we present a "click to self-immolation" strategy based on aroyl azide-capped SIP precursors, enabling the facile construction of diverse SIPs with different trigger units through a Curtius rearrangement and alcohol/thiol-isocyanate "click" reaction. This strategy is also applied to polymer-polymer coupling to access fully depolymerizable block copolymer amphiphiles, even combining different SIP backbones. Our results demonstrate that the depolymerization can be actuated efficiently under physiologically-relevant conditions by the removal of the trigger units and ensuing self-immolation of the p-aminobenzyl carbonate linkage, indicating promise for controlled release applications involving nanoparticles and hydrogels.

Keywords
Block Copolymer; Click Chemistry; Functionalization; Self-Immolative Polymer; Stimuli-Responsive.
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