Issue 41, 2018

The reductive aromatization of naphthalene diimide: a versatile platform for 2,7-diazapyrenes

Abstract

The reductive aromatization of naphthalene diimide provides tetrapivaloxy-2,7-diazapyrene, which serves as a versatile platform toward peripherally substituted 2,7-diazapyrenes. Time-resolved microwave conductivity measurements demonstrated that the intrinsic electron mobility of 2,7-diazapyrene is significantly higher than that of the corresponding pyrene.

Graphical abstract: The reductive aromatization of naphthalene diimide: a versatile platform for 2,7-diazapyrenes

Supplementary files

Article information

Article type
Communication
Submitted
10 Mar 2018
Accepted
05 Apr 2018
First published
06 Apr 2018

Chem. Commun., 2018,54, 5177-5180

The reductive aromatization of naphthalene diimide: a versatile platform for 2,7-diazapyrenes

T. Nakazato, T. Kamatsuka, J. Inoue, T. Sakurai, S. Seki, H. Shinokubo and Y. Miyake, Chem. Commun., 2018, 54, 5177 DOI: 10.1039/C8CC01937A

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