Cited time in webofscience Cited time in scopus

Full metadata record

DC Field Value Language
dc.contributor.author Cho, Soojeong -
dc.contributor.author Shin, Hyeon Min -
dc.contributor.author Jeong, Yeonwoo -
dc.contributor.author Kim, Sunhee -
dc.contributor.author Eom, Ji Hwan -
dc.contributor.author Jung, Byunghyuck -
dc.contributor.author Kang, Sung Min -
dc.contributor.author Cho, Woo Kyung -
dc.date.accessioned 2021-06-25T20:05:52Z -
dc.date.available 2021-06-25T20:05:52Z -
dc.date.created 2021-05-14 -
dc.date.issued 2021-05 -
dc.identifier.issn 1144-0546 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/13761 -
dc.description.abstract Polyphenols containing catechol (1,2-dihydroxyphenyl)/pyrogallol (1,2,3-trihydroxyphenyl) groups have been employed as precursors to prepare substrate-independent (i.e., universal) coatings. However, quercetin, an interesting flavonol due to its unique biological properties, was previously found to be an inefficient compound for substrate coatings after screening polyphenolic compounds. We report that quercetin-based thin films could be formed on various substrates, including titanium dioxide, silicon wafers, gold, nylon, and glass, when diethylenetriamine (DETA) was used as an additive. DETA acted as a cross-linker to facilitate conjugate addition and imine formation with the catechol in quercetin. The film thickness was controllable by changing the quercetin concentration. Static water contact angles for all examined substrates converged to 25° regardless of the vastly different static water contact angles of the bare substrates, showing the universal coating capability of quercetin and DETA. Importantly, the films formed with quercetin and DETA were chemically modifiable; thus, specific functions on the surface could be introduced. α-Bromoisobutyryl bromide was immobilized on the films via esterification, and then a zwitterionic sulfobetaine polymer was subsequently grafted. Compared to the controls, the polymer-grafted surface effectively suppressed the adsorption of fibrinogen and platelets, demonstrating its non-biofouling effect. Considering its universal coating and postfunctionalization capabilities, this quercetin-based film provides a route for the preparation of functional organic coatings. This journal is © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique. -
dc.language English -
dc.publisher Royal Society of Chemistry -
dc.title Plant-inspired quercetin thin films: universal coatings and their postfunctionalization for non-biofouling applications -
dc.type Article -
dc.identifier.doi 10.1039/d1nj00593f -
dc.identifier.wosid 000639417700001 -
dc.identifier.scopusid 2-s2.0-85105519961 -
dc.identifier.bibliographicCitation New Journal of Chemistry, v.45, no.17, pp.7533 - 7541 -
dc.description.isOpenAccess FALSE -
dc.citation.endPage 7541 -
dc.citation.number 17 -
dc.citation.startPage 7533 -
dc.citation.title New Journal of Chemistry -
dc.citation.volume 45 -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.relation.journalResearchArea Chemistry -
dc.relation.journalWebOfScienceCategory Chemistry, Multidisciplinary -
dc.type.docType Article -
Files in This Item:

There are no files associated with this item.

Appears in Collections:
Department of Physics and Chemistry Asymmetric Organic Synthesis and Drug Synthesis Laboratory 1. Journal Articles

qrcode

  • twitter
  • facebook
  • mendeley

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE