Influence of Positional Isomerism on the Chiroptical Properties of Functional Aromatic Oligoamide Foldamers.
circularly polarized luminescence
foldamers
oligoamides
positional isomerism
vibrational circular dichroism
Journal
ChemPlusChem
ISSN: 2192-6506
Titre abrégé: Chempluschem
Pays: Germany
ID NLM: 101580948
Informations de publication
Date de publication:
03 2021
03 2021
Historique:
revised:
08
03
2021
received:
01
02
2021
entrez:
23
3
2021
pubmed:
24
3
2021
medline:
24
3
2021
Statut:
ppublish
Résumé
A series of functionalized quinoline-based aromatic oligoamide foldamers were prepared in their two enantiomeric forms, comprising an enantiopure terminal camphanyl chiral inducer, which governed the adjacent (P-/M-) helical-handedness. Hierarchical chirality transfer was further investigated in chromophore-appended variants via a range of electronic and vibrational spectroscopic techniques, including circularly polarized luminescence, vibrational circular dichroism and fluorescence. Intense total and polarized photoluminescence (up to Φ
Identifiants
pubmed: 33755326
doi: 10.1002/cplu.202100051
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
496-503Subventions
Organisme : The University of Bordeaux
Organisme : IdEx Bordeaux
Informations de copyright
© 2021 Wiley-VCH GmbH.
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