Novel π-Conjugated Systems Based on N-Confused Porphyrinoids

Research output: Chapter in Book/Report/Conference proceedingChapter

2 Citations (Scopus)

Abstract

N-confused porphyrin (termed as NCP) is an isomer of porphyrin in which a pyrrole is connected to the neighboring meso-carbon atoms at α,β′-positions. The specific π-conjugated scaffold present in NCPs provides unique photophysical and electrochemical properties as well as abilities of metal complexation and anion binding in many cases. That has inspired us to explore the further synthetic approaches for development of novel class of porphyrin analogues based on “N-confusion concept.” This chapter introduces an overview of recent development in the chemistry of N-confused porphyrin and related macrocycles.

Original languageEnglish
Title of host publicationChemical Science of Electron Systems
PublisherSpringer Japan
Pages201-221
Number of pages21
ISBN (Electronic)9784431553571
ISBN (Print)9784431553564
DOIs
Publication statusPublished - Jan 1 2015

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Porphyrins
Pyrroles
Complexation
Electrochemical properties
Scaffolds
Isomers
Anions
Negative ions
Carbon
Metals
Atoms

All Science Journal Classification (ASJC) codes

  • Chemistry(all)
  • Engineering(all)
  • Biochemistry, Genetics and Molecular Biology(all)

Cite this

Novel π-Conjugated Systems Based on N-Confused Porphyrinoids. / Ishida, Masatoshi; Furuta, Hiroyuki.

Chemical Science of Electron Systems. Springer Japan, 2015. p. 201-221.

Research output: Chapter in Book/Report/Conference proceedingChapter

Ishida, Masatoshi ; Furuta, Hiroyuki. / Novel π-Conjugated Systems Based on N-Confused Porphyrinoids. Chemical Science of Electron Systems. Springer Japan, 2015. pp. 201-221
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