Cited by 582Polymer Surface Interaction StudiesConducting polymers and applicationsMarine Biology and Environmental Chemistry

Building‐Block Diversity in Polydopamine Underpins a Multifunctional Eumelanin‐Type Platform Tunable Through a Quinone Control Point

Della Vecchia, Nicola F., Avolio, Roberto, Alfè, Michela, Errico, Maria E., Napolitano, Alessandra, d'Ischia, Marco·2013·Advanced Functional Materials

Abstract

Rational approaches to engineering polydopamine films with tailored properties for surface coating and functionalization are currently challenged by the lack of detailed information about the polymer structure and the mechanism of buildup. Using an integrated chemical and spectroscopic approach enables the demonstration of: a) a three‐component structure of polydopamine, comprising uncyclized (catecholamine) and cyclized (indole) units, as well as novel pyrrolecarboxylic acid moieties; b) remarkable variations in the relative proportions of the cyclized and uncyclized units with starting dopamine concentration; c) the occurrence of oligomer components up to the tetramer level; d) the covalent incorporation of Tris buffer; and e) the role of dopamine quinone as a crucial control point for directing the buildup pathways and tuning the properties. The importance of the uncyclized amine‐containing units in polydopamine adhesion is also highlighted. The proper selection of substrate concentration and buffer is thus proposed as a practical means of tailoring polydopamine functionality via control of competing pathways downstream of dopamine quinone.

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Registry

Crossref · 10.1002/adfm.201202127

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2 of 2 references verified0 citation errors · 0 not checkable

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  • The second model is the "noncovalent bonding (quinhydrones)" polymerization fashion where DA monomers are linked together by noncovalent interaction including hydrogen bonding, charge transfer, ionic interaction, and π-stacking to aggregate into a structural macroassembly.

    “The second model is the “noncovalent bonding (quinhydrones)” polymerization fashion where DA monomers are linked together by noncovalent interaction including hydrogen bonding, charge transfer, ionic interaction, and π-stacking to aggregate into a structural macroassembly [35, 45–47].”

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Authors
Della Vecchia, N. F., Avolio, R., Alfè, M., Errico, M. E., Napolitano, A., & d'Ischia, M.
Affiliations
  • National Research Council (IT)
  • University of Naples Federico II (IT)
Venue
Advanced Functional Materials
Publisher
Wiley
Published
2012-10-09
Volume
23
Issue
10
Pages
1331-1340
ISSN
  • 1616-301X (ISSN-L)
  • 1616-3028
OpenAlex
W1970209371
Cited by
582
References
2
Citations by year
2026: 25 · 2025: 29 · 2024: 47 · 2023: 40 · 2022: 43 · 2021: 47 · 2020: 54 · 2019: 61 · 2018: 50 · 2017: 41 · 2016: 44 · 2015: 35 · 2014: 44 · 2013: 20 · 2012: 2
FWCI
14.27
Type
journal article
Language
en
Open access
closed
Locations
  • Advanced Functional Materials (publishedVersion)
  • Scuola Normale Superiore di Pisa (submittedVersion)
Topics
  • Physical Sciences › Materials Science › Surfaces, Coatings and Films › Polymer Surface Interaction Studies
  • Physical Sciences › Materials Science › Polymers and Plastics › Conducting polymers and applications
  • Physical Sciences › Engineering › Ocean Engineering › Marine Biology and Environmental Chemistry
Keywords
polydopamine, dopamine quinone, catecholamines, indole, oligomerization, polymer film structure, surface coating, surface functionalization, adhesion, polymerization pathways

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