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Catechols as versatile platforms in polymer chemistry
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“Using these classic organic reactions, the catechol group has been successfully incorporated into a series of natural polymers, such as PL, HA, chitosan, SA, and gelatin (GT), and synthetic polymers, such as polyethylene glycol (PEG)-based polymers [45,47,51,52,53,54,55].”
From Mussel-Inspired Injectable Adhesive Hydrogels for Biomedical Applications (2024) · cites this paper as [47]
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“During recent decades, many methods have been developed to incorporate the catechol group into polymers [4,47], including the incorporation of the catechol group by classic organic reactions, polymerization of catechol-based monomers, and biosynthesis of catechol-containing proteins (Figure 3).”
From Mussel-Inspired Injectable Adhesive Hydrogels for Biomedical Applications (2024) · cites this paper as [47]
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“On the one hand, this makes the mussel-inspired hydrogel suitable for eliminating ROS in the wound healing process.”
From Mussel-Inspired Injectable Adhesive Hydrogels for Biomedical Applications (2024) · cites this paper as [47]
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“Therefore, commonly, catechol is protected before polymerization [47].”
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“Second, the catechol group is a polymerization inhibitor with the capacity to react with free radicals [47].”
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Mussel-inspired surface chemistry for multifunctional coatings
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Dechy-Cabaret, O., Martin-Vaca, B., & Bourissou, D. (2004) · Chemical Reviews · doi:10.1021/cr040002s · Cited by 2,257
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Radical addition–fragmentation chemistry in polymer synthesis
Moad, G., Rizzardo, E., & Thang, S. H. (2008) · Polymer · doi:10.1016/j.polymer.2007.11.020 · Cited by 1,397
Polydopamine—a nature-inspired polymer coating for biomedical science
Lynge, M. E., van der Westen, R., Postma, A., & Städler, B. (2011) · Nanoscale · doi:10.1039/c1nr10969c · Cited by 907
Marrying click chemistry with polymerization: expanding the scope of polymeric materials
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Mussel‐Inspired Polydopamine Coating as a Universal Route to Hydroxyapatite Crystallization
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Characterization of Dopamine−Melanin Growth on Silicon Oxide
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Metadata
- Authors
- Faure, E., Falentin-Daudré, C., Jérôme, C., Lyskawa, J., Fournier, D., Woisel, P., & Detrembleur, C.
- Affiliations
- University of Liège (BE)
- Unité Matériaux et Transformations (FR)
- École Nationale Supérieure de Chimie de Lille (FR)
- Corresponding author
- Woisel, Patrice
- Detrembleur, Christophe
- ORCID
- Venue
- Progress in Polymer Science
- Publisher
- Elsevier BV
- Published
- 2013-01
- Volume
- 38
- Issue
- 1
- Pages
- 236-270
- ISSN
- 0079-6700 (ISSN-L)
- OpenAlex
- W2134995275
- Cited by
- 616
- References
- 0
- Citations by year
- 2026: 21 · 2025: 45 · 2024: 42 · 2023: 45 · 2022: 36 · 2021: 48 · 2020: 54 · 2019: 57 · 2018: 64 · 2017: 56 · 2016: 40 · 2015: 49 · 2014: 42 · 2013: 14
- FWCI
- 14.98
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Progress in Polymer Science (publishedVersion)
- ORBi (University of Liège) (submittedVersion, other-oa)
- Funders
- Waalse Gewest
- Fonds De La Recherche Scientifique - FNRS
- Belgian Federal Science Policy Office
- Topics
- Physical Sciences › Materials Science › Surfaces, Coatings and Films › Polymer Surface Interaction Studies
- Physical Sciences › Chemistry › Organic Chemistry › Advanced Polymer Synthesis and Characterization
- Physical Sciences › Materials Science › Polymers and Plastics › Epoxy Resin Curing Processes
- Keywords
- catechol, mussel-inspired adhesives, synthetic adhesives, surface coating, surface modification, anchoring groups, pendant groups, end-functionalized polymers, polymer synthesis
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