Literature DB >> 29637960

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

Takumi Nakazato1, Takuto Kamatsuka, Junichi Inoue, Tsuneaki Sakurai, Shu Seki, Hiroshi Shinokubo, Yoshihiro Miyake.   

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.

Entities:  

Year:  2018        PMID： 29637960     DOI： 10.1039/c8cc01937a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  2 in total

Review 1.  2,7-Diazapyrenes: a brief review on synthetic strategies and application opportunities.

Authors:  Anindita Mukherjee; Alexey A Akulov; Sougata Santra; Mikhail V Varaksin; Grigory A Kim; Dmitry S Kopchuk; Olga S Taniya; Grigory V Zyryanov; Oleg N Chupakhin
Journal:  RSC Adv       Date:  2022-03-24       Impact factor: 3.361

2.  A Highly Luminescent Nitrogen-Doped Nanographene as an Acid- and Metal-Sensitive Fluorophore for Optical Imaging.

Authors:  Enquan Jin; Qiqi Yang; Cheng-Wei Ju; Qiang Chen; Katharina Landfester; Mischa Bonn; Klaus Müllen; Xiaomin Liu; Akimitsu Narita
Journal:  J Am Chem Soc       Date:  2021-07-05       Impact factor: 15.419
  2 in total

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