Force-induced cleavage of a labile bond for enhanced mechanochemical crosslinking
Literature Information
Publication Date
2017-10-03
DOI
10.1039/C7PY01431G
Impact Factor
5.582
Authors
Shu Wang, Grant A. Knappe, Norman J. Wagner
View Original
Abstract
We introduce a simple, yet powerful approach towards force-induced healing polymers. While most synthetic polymers fail in response to stress and have no recovery mechanism, we demonstrate that polymers containing a thiocarbonylthio group exhibit amplified mechanochemical activity. In the presence of a crosslinker, the radicals generated from homolytic cleavage are exploited to trigger a ‘healing’ response within minutes.
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Source Journal
Polymer Chemistry
CiteScore:
8.6
Self-citation Rate:
7.3%
Articles per Year:
457
Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.
Recommended Compounds
6-Bromo-3,4-dihydro-2H-1,4-benzoxazine hydrochloride (1:1)
CAS Number:
1260803-10-8
Molecular Formula:
C8H9BrClNO
![S-[2,3-Bis(palmitoyloxy)propyl]-N-[(9H-fluoren-9-ylmethoxy)(hydroxy)methylene]cysteine structure](https://static.chemtradehub.com/structs/210/210532-98-2-f6a7.webp "S-[2,3-Bis(palmitoyloxy)propyl]-N-[(9H-fluoren-9-ylmethoxy)(hydroxy)methylene]cysteine structure")
S-[2,3-Bis(palmitoyloxy)propyl]-N-[(9H-fluoren-9-ylmethoxy)(hydroxy)methylene]cysteine
CAS Number:
210532-98-2
Molecular Formula:
C53H83NO8S
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