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Cyclic Ether Triggers for Polymeric Frustrated Lewis Pair Gels

[Image: see text] Sterically hindered Lewis acid and base centers are unable to form Lewis adducts, instead forming frustrated Lewis pairs (FLPs), where latent reactivity can be utilized for the activation of small molecules. Applying FLP chemistry into polymeric frameworks transforms this chemistry...

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Autores principales: Yolsal, Utku, Horton, Thomas A. R., Wang, Meng, Shaver, Michael P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397318/
https://www.ncbi.nlm.nih.gov/pubmed/34387464
http://dx.doi.org/10.1021/jacs.1c06408
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author Yolsal, Utku
Horton, Thomas A. R.
Wang, Meng
Shaver, Michael P.
author_facet Yolsal, Utku
Horton, Thomas A. R.
Wang, Meng
Shaver, Michael P.
author_sort Yolsal, Utku
collection PubMed
description [Image: see text] Sterically hindered Lewis acid and base centers are unable to form Lewis adducts, instead forming frustrated Lewis pairs (FLPs), where latent reactivity can be utilized for the activation of small molecules. Applying FLP chemistry into polymeric frameworks transforms this chemistry into responsive and functional materials. Here, we report a versatile synthesis strategy for the preparation of macromolecular FLPs and explore its potential with the ring-opening reactions of cyclic ethers. Addition of the cyclic substrates triggered polymer network formation, where the extent of cross-linking, strength of network, and reactivity are tuned by the steric and electronic properties of the ethers. The resultant networks behave like covalently cross-linked polymers, demonstrating the versatility of FLPs to simultaneously tune both small-molecule capture and mechanical properties of materials.
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spelling pubmed-83973182021-08-31 Cyclic Ether Triggers for Polymeric Frustrated Lewis Pair Gels Yolsal, Utku Horton, Thomas A. R. Wang, Meng Shaver, Michael P. J Am Chem Soc [Image: see text] Sterically hindered Lewis acid and base centers are unable to form Lewis adducts, instead forming frustrated Lewis pairs (FLPs), where latent reactivity can be utilized for the activation of small molecules. Applying FLP chemistry into polymeric frameworks transforms this chemistry into responsive and functional materials. Here, we report a versatile synthesis strategy for the preparation of macromolecular FLPs and explore its potential with the ring-opening reactions of cyclic ethers. Addition of the cyclic substrates triggered polymer network formation, where the extent of cross-linking, strength of network, and reactivity are tuned by the steric and electronic properties of the ethers. The resultant networks behave like covalently cross-linked polymers, demonstrating the versatility of FLPs to simultaneously tune both small-molecule capture and mechanical properties of materials. American Chemical Society 2021-08-13 2021-08-25 /pmc/articles/PMC8397318/ /pubmed/34387464 http://dx.doi.org/10.1021/jacs.1c06408 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Yolsal, Utku
Horton, Thomas A. R.
Wang, Meng
Shaver, Michael P.
Cyclic Ether Triggers for Polymeric Frustrated Lewis Pair Gels
title Cyclic Ether Triggers for Polymeric Frustrated Lewis Pair Gels
title_full Cyclic Ether Triggers for Polymeric Frustrated Lewis Pair Gels
title_fullStr Cyclic Ether Triggers for Polymeric Frustrated Lewis Pair Gels
title_full_unstemmed Cyclic Ether Triggers for Polymeric Frustrated Lewis Pair Gels
title_short Cyclic Ether Triggers for Polymeric Frustrated Lewis Pair Gels
title_sort cyclic ether triggers for polymeric frustrated lewis pair gels
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397318/
https://www.ncbi.nlm.nih.gov/pubmed/34387464
http://dx.doi.org/10.1021/jacs.1c06408
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