Oxidation State-Dependent Intramolecular Electronic Interaction of Carbazole-Based Azacyclophanes with 9,10-Anthrylene Units.
J Org Chem
; 82(19): 10699-10703, 2017 10 06.
Article
em En
| MEDLINE
| ID: mdl-28881128
ABSTRACT
We designed an azacyclophane comprising 3,6-substituted carbazole and 9,10-anthrylene units to investigate the unique electronic properties of the oxidation states arising from the presence of multiple oxidizable azacyclophane. This compound and its analogue containing 1,4-phenylene in substitution of 9,10-anthrylene units were synthesized by Buchwald-Hartwig coupling reactions. Cyclic voltammograms of both the 9,10-anthrylene and 1,4-phenylene derivatives exhibited four quasi-reversible oxidation processes. The absorption spectra of the oxidation states of the 9,10-anthrylene derivative exhibited broad absorption bands in the near-infrared region arising from charge-resonance and intramolecular charge-transfer interactions. The photophysical and electrochemical properties of the 9,10-anthrylene derivative were compared with those of the corresponding 1,4-phenylene derivative on the basis of theoretical calculations to evaluate the intramolecular electronic interactions.
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1
Coleções:
01-internacional
Base de dados:
MEDLINE
Idioma:
En
Revista:
J Org Chem
Ano de publicação:
2017
Tipo de documento:
Article
País de afiliação:
Japão