One-pot blue-light triggered tough interpenetrating polymeric network (IPN) using CuAAC and methacrylate reactions
Literature Information
Publication Date
2017-05-08
DOI
10.1039/C7PY00623C
Impact Factor
5.582
Authors
Abhishek U. Shete
View Original
Abstract
An interpenetrating polymeric network (IPN) is formed in a one-pot blue-light activated scheme, where the step- and chain-growth polymerizations of the CuAAC and methacrylate reactions, respectively, are simultaneously triggered but proceed sequentially. The glassy IPN is polymerized under ambient conditions and is able to withstand high strain before failure owing to its significantly enhanced toughness. Additionally, this material exhibits shape memory attributes with readily tunable mechanical properties at high temperature.
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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
(3beta,7beta,12beta)-3,7,12-Trihydroxy-11,15,23-trioxolanost-8-en-26-oic acid
CAS Number:
98665-22-6
Molecular Formula:
C30H44O8
![1,2-Diphenyl-4-[2-(phenylsulfinyl)ethyl]-3,5-pyrazolidinedione structure](https://static.chemtradehub.com/structs/57-/57-96-5-efcc.webp "1,2-Diphenyl-4-[2-(phenylsulfinyl)ethyl]-3,5-pyrazolidinedione structure")
1,2-Diphenyl-4-[2-(phenylsulfinyl)ethyl]-3,5-pyrazolidinedione
CAS Number:
57-96-5
Molecular Formula:
C23H20N2O3S
![N-[(Benzyloxy)carbonyl]serine structure](https://static.chemtradehub.com/structs/276/2768-56-1-77f7.webp "N-[(Benzyloxy)carbonyl]serine structure")
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