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Abstract
Steric bulk prevents the formation of strong bonds between Lewis acids and bases in frustrated Lewis pairs (FLPs), where latent reactivity makes these reagents transformative in small molecule activations and metal-free catalysis. How-ever, their use as a platform for developing materials chemistry is unexplored. Here we report a fully macromolecular FLP, built from linear copolymers that containing either a sterically encumbered Lewis base or Lewis acid as a pendant functional group. The target functional copolymers were prepared by a controlled radical copolymerization of styrene with designer boron or phosphorus containing monomers. Mixtures of the B- and P-functionalized polystyrenes do not react, with the steric bulk of the functional monomers preventing the favorable Lewis acid base interaction. Addition of a small molecule (diethyl azodicarboxylate) promotes rapid network formation, crosslinking the reactive polymer chains. The resulting gel is dynamic, can self-heal, is heat responsive, and can be reshaped by post-gelation processing.
Original language | English |
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Pages (from-to) | 14232–14236 |
Number of pages | 5 |
Journal | Journal of the American Chemical Society |
Volume | 139 |
Issue number | 40 |
Early online date | 15 Sept 2017 |
DOIs | |
Publication status | Published - 11 Oct 2017 |
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Dive into the research topics of 'Frustrated Lewis Pair Polymers as Responsive Self-Healing Gels'. Together they form a unique fingerprint.Projects
- 1 Finished
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Coordination Chemistry Inspired Advances in Controlled Radical Polymerisation
Shaver, M.
15/09/14 → 14/12/17
Project: Research
Profiles
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Fabio Nudelman
- School of Chemistry - Personal Chair of Biomineralization
- EaStCHEM
- Centre for Engineering Biology
Person: Academic: Research Active