The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Competition between Oxidation and Coordination in Cross-Linking of Polystyrene Copolymer Containing Catechol Groups
Abstract
In gelation chemistry, catechol groups are used as cross-linking points. Both oxidation and coordination effects of catechol were investigated for their unique features in chemistry by spectroscopic measurements. Polystyrene copolymers containing catechol groups were synthesized by free radical copolymerization of styrene and N -2-(3′,4′-ditriethylsilyloxyphenyl)ethyl methacrylamide, and the successive deprotection reaction was catalyzed by tetra- n -butylammonium fluoride. The copolymer containing catechol units afforded a dual cross-linking system based on completely different coordination and oxidation chemistries, and the competing cross-linking mechanisms are discussed. These findings are useful and important for paving the way for designing a novel bioinspired artificial adhesive surface coating and curing system.
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Cites
Mussel-inspired surface chemistry for multifunctional coatings
Lee, H., Dellatore, S. M., Miller, W. M., & Messersmith, P. B. (2007) · Science · doi:10.1126/science.1147241 · Cited by 10,965
Holten-Andersen, N., Harrington, M. J., Birkedal, H., Lee, B. P., Messersmith, P. B., Lee, K. Y. C., & Waite, J. H. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1015862108 · Cited by 1,597
Cross-Linking in Adhesive Quinoproteins: Studies with Model Decapeptides
Burzio, L. A., & Waite, J. H. (2000) · Biochemistry · doi:10.1021/bi0002434 · Cited by 485
Papov, V. V., Diamond, T. V., Biemann, K., & Waite, J. H. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.34.20183 · Cited by 329
Cited by
Zhao, X., Liang, Y., Huang, Y., He, J., Han, Y., & Guo, B. (2020) · Advanced Functional Materials · doi:10.1002/adfm.201910748 · Cited by 814
Mussel-inspired hydrogels: From design principles to promising applications
Zhang, C., Wu, B., Zhou, Y., Zhou, F., Liu, W., & Wang, Z. (2020) · Chemical Society Reviews · doi:10.1039/c9cs00849g · Cited by 653
Liu, Y., Zhu, Z., Pei, X., Zhang, X., Cheng, X., Hu, S., Gao, X., Wang, J., Chen, J., & Wan, Q. (2020) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.0c12090 · Cited by 259
Robust, self-healing hydrogels synthesised from catechol rich polymers
Yavvari, P. S., & Srivastava, A. (2015) · Journal of Materials Chemistry B · doi:10.1039/c4tb01307g · Cited by 126
Lee, J., Chang, K., Kim, S., Gite, V., Chung, H., & Sohn, D. (2016) · Macromolecules · doi:10.1021/acs.macromol.6b01198 · Cited by 122
Metadata
- Authors
- Xu, H., Nishida, J., Ma, W., Wu, H., Kobayashi, M., Otsuka, H., & Takahara, A.
- Venue
- ACS Macro Letters
- Publisher
- American Chemical Society (ACS)
- Published
- 2012-03-19
- Volume
- 1
- Issue
- 4
- Pages
- 457-460
- ISSN
- 2161-1653 (ISSN-L)
- OpenAlex
- W2011625425
- Cited by
- 187
- References
- 4
- FWCI
- 6.42
- Type
- journal article
- Language
- en
- Open access
- closed
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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