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Cited by 56Advanced NMR Techniques and ApplicationsInorganic and Organometallic ChemistryElectron Spin Resonance Studies

CPMAS (cross-polarization magic angle spinning) carbon-13 NMR spectra of quinones, hydroquinones, and their complexes. Use of CMR to follow a reaction in the solid state

Scheffer, J., Wong, Y. F., Patil, A. O., Curtin, D. Y., Paul, I. C.·1985·Journal of the American Chemical Society
DOI 10.1021/ja00303a014
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Abstract

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTCPMAS (cross-polarization magic angle spinning) carbon-13 NMR spectra of quinones, hydroquinones, and their complexes. Use of CMR to follow a reaction in the solid stateJ. Scheffer, Y. F. Wong, A. O. Patil, D. Y. Curtin, and I. C. PaulCite this: J. Am. Chem. Soc. 1985, 107, 17, 4898–4904Publication Date (Print):August 1, 1985Publication History Published online1 May 2002Published inissue 1 August 1985https://pubs.acs.org/doi/10.1021/ja00303a014https://doi.org/10.1021/ja00303a014research-articleACS PublicationsRequest reuse permissionsArticle Views902Altmetric-Citations45LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and a…

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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].”

    From Polydopamine-Assisted Surface Modification for Bone Biosubstitutes (2016) · cites this paper as [47]

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Sorted by citations

Authors
Scheffer, J., Wong, Y. F., Patil, A. O., Curtin, D. Y., & Paul, I. C.
ORCID
Curtin, D. Y.
Venue
Journal of the American Chemical Society
Publisher
American Chemical Society (ACS)
Published
1985-08
Volume
107
Issue
17
Pages
4898-4904
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
DOI
10.1021/ja00303a014
OpenAlex
W2047443504
Cited by
56
References
0
Citations by year
2026: 1 · 2025: 1 · 2024: 4 · 2023: 1 · 2022: 1 · 2021: 1 · 2020: 4 · 2019: 2 · 2016: 4 · 2015: 4 · 2013: 3
FWCI
1.75
Type
journal article
Language
en
Open access
closed
Locations
Journal of the American Chemical Society (publishedVersion)
Topics
  • Physical Sciences › Chemistry › Spectroscopy › Advanced NMR Techniques and Applications
  • Physical Sciences › Chemistry › Organic Chemistry › Inorganic and Organometallic Chemistry
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Biophysics › Electron Spin Resonance Studies
Keywords
quinones, hydroquinone, 13C NMR, cross-polarization magic angle spinning

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