Aromatic and Antiaromatic Pathways in Triphyrin(2.1.1) Annelated with Benzo[b]heterocycles.
acenes
antiaromaticity
aromaticity
chirality
triphyrin
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 Dec 2019
05 Dec 2019
Historique:
received:
23
08
2019
pubmed:
20
9
2019
medline:
20
9
2019
entrez:
20
9
2019
Statut:
ppublish
Résumé
Understanding of the aromatic properties and magnetically induced current densities of highly conjugated chromophores is important when designing molecules with strongly delocalized electronic structure. Linear extension of the triphyrin(2.1.1) skeleton with an annelated benzo[b]heterocycle fragment modifies the aromatic character by extending the electron delocalization pathway. Two-electron reduction leads to an antiaromatic triphyrin(2.1.1) ring and an aromatic benzo[b]heterocycle subunit. Current-density calculations provide detailed information about the observed pathways and their strengths.
Identifiants
pubmed: 31535404
doi: 10.1002/chem.201903863
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
15477-15482Subventions
Organisme : Narodowe Centrum Nauki
ID : 2015/17/B/ST5/01437
Informations de copyright
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
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