A Direct Method to Access Substituted Pyreno[4,5-c:9,10-c′] difuran and its Analogues

Research output: Journal Publications and Reviews (RGC: 21, 22, 62)21_Publication in refereed journalpeer-review

3 Scopus Citations
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Author(s)

  • Wangqiao Chen
  • Guankui Long
  • Koji Kanehira
  • Mingtao Zhang
  • Tsuyoshi Michinobu
  • Ming Liu

Detail(s)

Original languageEnglish
Pages (from-to)2213-2217
Journal / PublicationAsian Journal of Organic Chemistry
Volume7
Issue number11
Online published23 Mar 2018
Publication statusPublished - Nov 2018
Externally publishedYes

Abstract

In this research, pyreno[4,5-c:9,10-c′]difuran and its analogues have been successfully synthesized through a one-step reaction using the same precursor and their physicochemical properties were studied. UV/Vis, fluorescence and CV measurements illustrated that the inserted chalcogen atoms (O, S and Se) brought almost no change on the photochemical and electrochemical properties whereas TM-2N-CH3 exhibited more blue-shifted fluorescence emission and simultaneously elevated HOMO energy level.

Research Area(s)

  • isoarene, lawesson's reagent, pyrene, pyreno[4,5-c:9,10-c′]difuran, woollins’ reagent

Citation Format(s)

A Direct Method to Access Substituted Pyreno[4,5-c:9,10-c′] difuran and its Analogues. / Chen, Wangqiao; Long, Guankui; Kanehira, Koji; Zhang, Mingtao; Michinobu, Tsuyoshi; Liu, Ming; Zhang, Qichun.

In: Asian Journal of Organic Chemistry, Vol. 7, No. 11, 11.2018, p. 2213-2217.

Research output: Journal Publications and Reviews (RGC: 21, 22, 62)21_Publication in refereed journalpeer-review