Visualization and quantitation of electronic communication pathways in a series of redox-active pillar[6]arene-based macrocycles.
Journal
Communications chemistry
ISSN: 2399-3669
Titre abrégé: Commun Chem
Pays: England
ID NLM: 101725670
Informations de publication
Date de publication:
13 Aug 2020
13 Aug 2020
Historique:
received:
04
05
2020
accepted:
23
07
2020
entrez:
27
1
2023
pubmed:
13
8
2020
medline:
13
8
2020
Statut:
epublish
Résumé
While oxidized pillar[5]arenes with 1-5 benzoquinone units are known, very few examples of oxidized pillar[6]arenes have been reported. We describe here the synthesis, characterization and electrochemical behavior of a series of macrocyclic hosts prepared by the stepwise oxidation of 1,4-diethoxypillar[6]arene, resulting in high-yield and high-purity isolation of two constitutional isomers for each macrocycle, in which two, three or four 1,4-diethoxybenzene units are replaced by benzoquinone residues. A careful structural comparison with their counterparts in the pillar[5]arene framework indicates that the geometries of the macrocycles are better described as non-Euclidean hyperbolic hexagons and elliptic pentagons, respectively. A comprehensive computational study to determine anisotropic induced current density (ACID) allows us to visualize and quantify through-space and through-bond communication pathways along the macrocyclic belt. Experimental and simulated voltammetric data, as well as UV-vis spectra, of the new macrocycles afford insights into the various electronic communication pathways in these compounds.
Identifiants
pubmed: 36703347
doi: 10.1038/s42004-020-00363-4
pii: 10.1038/s42004-020-00363-4
pmc: PMC9814560
doi:
Types de publication
Journal Article
Langues
eng
Pagination
117Subventions
Organisme : National Science Foundation (NSF)
ID : CHE-1412455
Informations de copyright
© 2020. The Author(s).
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