Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Quercetin and its analogues: optical and acido-basic properties
KTH, School of Biotechnology (BIO), Theoretical Chemistry and Biology.
Show others and affiliations
2017 (English)In: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 19, no 39, p. 26870-26879Article in journal (Refereed) Published
Abstract [en]

This study is focused on eight structurally analogous natural flavonoids that exhibit a wide range of biological activities, which are of interest in pharmacy, cosmetics and the food industry. Using both experimental and theoretical approaches, we relate their fundamental physico-chemical properties to the structural motifs, with particular focus on UV/Vis absorption properties and pH dependence. We highlight the role of the C2-C3 double bond, whose presence or absence is responsible for the switch between absorption bands in the UVB and UVA regions, which is rationalized by strong modification of the involved molecular orbitals. After deprotonation in an alkaline environment, a typical switch in intensity at the maximum absorption wavelength (lambda(max)) is observed enabling the calculation of pK(a) values for compounds with a C2-C3 single bond, whereas a bathochromic shift of lambda(max) vs. pH is observed for the C2-C3 double bond containing compounds. These behaviors are also rationalized and understood by MO analysis. Interestingly, high pH (above 11 for ampelopsin and above 9 for myricetin) induces the formation of a long-wavelength peak arising from double and/or triple deprotonation. Substitution at position C3 by the OH group has almost no effect on lambda(max) for taxifolin and eriodictyol, whereas the effect is larger for quercetin and luteolin. An additional sugar moiety at C3 has a stabilizing effect and induces only minor changes in spectral behavior.

Place, publisher, year, edition, pages
ROYAL SOC CHEMISTRY , 2017. Vol. 19, no 39, p. 26870-26879
National Category
Other Chemistry Topics
Identifiers
URN: urn:nbn:se:kth:diva-217032DOI: 10.1039/c7cp03845cISI: 000412763700041PubMedID: 28952614Scopus ID: 2-s2.0-85031317204OAI: oai:DiVA.org:kth-217032DiVA, id: diva2:1160129
Note

QC 20171124

Available from: 2017-11-24 Created: 2017-11-24 Last updated: 2017-11-24Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textPubMedScopus

Authority records BETA

Biler, Michal

Search in DiVA

By author/editor
Biler, Michal
By organisation
Theoretical Chemistry and Biology
In the same journal
Physical Chemistry, Chemical Physics - PCCP
Other Chemistry Topics

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 52 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf