2- and 2,7-Substituted para-N-Methylpyridinium Pyrenes: Syntheses, Molecular and Electronic Structures, Photophysical, Electrochemical, and Spectroelectrochemical Properties and Binding to Double-Stranded (ds) DNA.
chromophores
luminescent
pyrenes
pyridinium
viologens
Journal
Chemistry (Weinheim an der Bergstrasse, Germany)
ISSN: 1521-3765
Titre abrégé: Chemistry
Pays: Germany
ID NLM: 9513783
Informations de publication
Date de publication:
05 Feb 2021
05 Feb 2021
Historique:
received:
28
10
2020
pubmed:
25
11
2020
medline:
25
11
2020
entrez:
24
11
2020
Statut:
ppublish
Résumé
Two N-methylpyridinium compounds and analogous N-protonated salts of 2- and 2,7-substituted 4-pyridyl-pyrene compounds were synthesised and their crystal structures, photophysical properties both in solution and in the solid state, electrochemical and spectroelectrochemical properties were studied. Upon methylation or protonation, the emission maxima are significantly bathochromically shifted compared to the neutral compounds, although the absorption maxima remain almost unchanged. As a result, the cationic compounds show very large apparent Stokes shifts of up to 7200 cm
Identifiants
pubmed: 33231335
doi: 10.1002/chem.202004748
pmc: PMC7898908
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2837-2853Subventions
Organisme : Bayerisches Staatsministerium für Bildung und Kultus, Wissenschaft und Kunst
ID : Collaborative Research Network "Solar Technologies go Hybrid"
Organisme : DFG
ID : GRK 2112
Organisme : Julius-Maximilians Universität Würzburg
Organisme : Croatian Science Foundation
ID : IP-2018-01-5475
Organisme : Alexander von Humboldt-Stiftung
Organisme : DAAD
Informations de copyright
© 2020 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH.
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