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Cyclic Ether Triggers for Polymeric Frustrated Lewis Pair Gels
Author(s) -
Utku Yolsal,
Thomas A. R. Horton,
Meng Wang,
Michael P. Shaver
Publication year - 2021
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.1c06408
Subject(s) - frustrated lewis pair , steric effects , chemistry , reactivity (psychology) , lewis acids and bases , covalent bond , adduct , macromolecule , molecule , polymer , ether , small molecule , polymer chemistry , combinatorial chemistry , organic chemistry , catalysis , medicine , biochemistry , alternative medicine , pathology
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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