Synthesis of Redox-switchable 5,15-Dialkyl-10,20-diaryl-5,15-diazaporphyrins and Diversification of their N-Alkyl Groups

Mai Mutoh, Keisuke Sudoh, Ko Furukawa, Mao Minoura, Haruyuki Nakano, Yoshihiro Matano

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Nickel(II) and copper(II) complexes of redox-switchable 20π, 19π, and 18π 5,15-dialkyl-10,20-diaryl-5,15-diazaporphyrins were prepared through a metal-templated cyclization method. Furthermore, the terminal silyloxy groups in the peripheral N-alkyl chains were transformed into hydroxy groups by deprotection. It is worth noting that redox reactions between the 19π and 18π systems bearing hydroxy groups caused a change in the water solubility of the diazaporphyrin chromophore.

Original languageEnglish
Pages (from-to)352-355
Number of pages4
JournalAsian Journal of Organic Chemistry
Volume8
Issue number3
DOIs
Publication statusPublished - Mar 1 2019

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Bearings (structural)
Redox reactions
Cyclization
Chromophores
Nickel
Copper
Solubility
Metals
Water
Oxidation-Reduction

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

Synthesis of Redox-switchable 5,15-Dialkyl-10,20-diaryl-5,15-diazaporphyrins and Diversification of their N-Alkyl Groups. / Mutoh, Mai; Sudoh, Keisuke; Furukawa, Ko; Minoura, Mao; Nakano, Haruyuki; Matano, Yoshihiro.

In: Asian Journal of Organic Chemistry, Vol. 8, No. 3, 01.03.2019, p. 352-355.

Research output: Contribution to journalArticle

Mutoh, Mai ; Sudoh, Keisuke ; Furukawa, Ko ; Minoura, Mao ; Nakano, Haruyuki ; Matano, Yoshihiro. / Synthesis of Redox-switchable 5,15-Dialkyl-10,20-diaryl-5,15-diazaporphyrins and Diversification of their N-Alkyl Groups. In: Asian Journal of Organic Chemistry. 2019 ; Vol. 8, No. 3. pp. 352-355.
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