Planarized B,N-phenylated dibenzoazaborine with a carbazole substructure: electronic impact of the structural constraint.


Journal

Organic & biomolecular chemistry
ISSN: 1477-0539
Titre abrégé: Org Biomol Chem
Pays: England
ID NLM: 101154995

Informations de publication

Date de publication:
05 Jun 2019
Historique:
pubmed: 22 5 2019
medline: 22 5 2019
entrez: 22 5 2019
Statut: ppublish

Résumé

A B,N-diphenyl-5,10-dihydro-dibenzo-1,4-azaborine, in which both phenyl groups on the boron and nitrogen atoms are planarized to generate a carbazole substructure, was synthesized. The structral constraint around the boron and nitrogen atoms alters the π-conjugation mode and thus the photophysical and electrochemical properties. Specifically, this structurally constrained dibenzoazaborine showed an intense blue emission with a narrow full width at half maximum. One of its derivatives exhibited near infrared absorption in the one-electron-oxidized state.

Identifiants

pubmed: 31112202
doi: 10.1039/c9ob00934e
doi:

Types de publication

Journal Article

Langues

eng

Pagination

5500-5504

Auteurs

Mikinori Ando (M)

Department of Chemistry, Graduate School of Science, Nagoya University, Furo, Chikusa, Nagoya, 464-8602, Japan.

Classifications MeSH