The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Mussel-Inspired Chemistry for Robust and Surface-Modifiable Multilayer Films
Abstract
In this article, we report a bioinspired approach to preparing stable, functional multilayer films by the integration of mussel-inspired catechol oxidative chemistry into a layer-by-layer (LbL) assembly. A polyanion of poly(acrylic acid-g-dopamine) (PAA-dopamine) bearing catechol groups, a mussel adhesive protein-mimetic polymer, was synthesized as the building block for LbL assembly with poly(allylamine hydrochloride) (PAH). The oxidization of the incorporated catechol group under mild oxidative condition yields o-quinone, which exhibits high reactivity with amine and catechol, thus endowing the chemical covalence and retaining the assembled morphology of multilayer films. The cross-linked films showed excellent stability even in extremely acidic, basic, and highly concentrated aqueous salt solutions. The efficient chemical cross-linking allows for the production of intact free-standing films without using a sacrificial layer. Moreover, thiol-modified multilayer films with good stability were exploited by a combination of thiols-catechol addition and then oxidative cross-linking. The outstanding stability under harsh conditions and the facile functionalization of the PAA-dopamine/PAH multilayer films make them attractive for barriers, separation, and biomedical devices.
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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
Strong reversible Fe 3+ -mediated bridging between dopa-containing protein films in water
Zeng, H., Hwang, D. S., Israelachvili, J. N., & Waite, J. H. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1007416107 · Cited by 517
Metal‐Mediated Cross‐Linking in the Generation of a Marine‐Mussel Adhesive
Sever, M. J., Weisser, J. T., Monahan, J., Srinivasan, S., & Wilker, J. J. (2004) · Angewandte Chemie International Edition · doi:10.1002/anie.200352759 · Cited by 486
Cited by
Liu, Y., Ai, K., & Lu, L. (2014) · Chemical Reviews · doi:10.1021/cr400407a · Cited by 4,794
The chemistry behind catechol-based adhesion
Saiz‐Poseu, J., Mancebo‐Aracil, J., Nador, F., Busqué, F., & Ruiz‐Molina, D. (2019) · Angewandte Chemie International Edition · doi:10.1002/anie.201801063 · Cited by 850
Layer-by-layer Nanoarchitectonics: Invention, Innovation, and Evolution
Ariga, K., Yamauchi, Y., Rydzek, G., Ji, Q., Yonamine, Y., Wu, K. C.-W., & Hill, J. P. (2014) · Chemistry Letters · doi:10.1246/cl.130987 · Cited by 850
Catechols as versatile platforms in polymer chemistry
Faure, E., Falentin-Daudré, C., Jérôme, C., Lyskawa, J., Fournier, D., Woisel, P., & Detrembleur, C. (2013) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2012.06.004 · Cited by 616
Tannic acid: a crosslinker leading to versatile functional polymeric networks: a review
Chen, C., Yang, H., Yang, X., & Ma, Q. (2022) · RSC Advances · doi:10.1039/d1ra07657d · Cited by 561
Metadata
- Authors
- Wu, J., Zhang, L., Wang, Y., Long, Y., Gao, H., Zhang, X., Zhao, N., Cai, Y., & Xu, J.
- Venue
- Langmuir
- Publisher
- American Chemical Society (ACS)
- Published
- 2011-10-24
- Volume
- 27
- Issue
- 22
- Pages
- 13684-13691
- ISSN
- 0743-7463 (ISSN-L)
- 1520-5827
- OpenAlex
- W2323773786
- Cited by
- 217
- References
- 3
- FWCI
- 6.16
- Type
- journal article
- Language
- en
- Open access
- closed
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