Highly planar diarylamine-fused porphyrins and their remarkably stable radical cations

Norihito Fukui, Wonhee Cha, Daiki Shimizu, Juwon Oh, Ko Furukawa, Hideki Yorimitsu, Dongho Kim, Atsuhiro Osuka

Research output: Contribution to journalArticle

28 Citations (Scopus)

Abstract

Oxidative fusion reactions of meso-phenoxazino Ni(ii) porphyrin were found to be temperature dependent, giving rise to either a doubly phenylene-fused product at room temperature or a singly phenoxazine-fused product at 70 °C. The latter was further oxidized to a doubly phenoxazine-fused Ni(ii) porphyrin, which was subsequently converted to the corresponding free base porphyrin and Zn(ii) porphyrin. Compared to previously reported diphenylamine-fused porphyrins that displayed a molecular twist, doubly phenoxazine-fused porphyrins exhibited distinctly different properties owing to their highly planar structures, such as larger fluorescence quantum yields, formation of an offset face-to-face dimer both in solution and the solid state, and the generation of a mixed-valence π-radical cation dimer upon electrochemical oxidation. One-electron oxidation of the phenoxazine-fused Ni(ii) porphyrin with Magic Blue gave the corresponding radical cation, which was certainly stable and could be isolated by separation over a silica gel column but slowly chlorinated at the reactive β-positions in the solid state. This finding led to us to examine β,β′-dichlorinated phenoxazine-fused and diphenylamine-fused Ni(ii) porphyrins, which, upon treatment with Magic Blue, provided remarkably stable radical cations to an unprecedented level. It is actually possible to purify these radical cations by silica gel chromatography, and they can be stored for over 6 months without any sign of deterioration. Moreover, they exhibited no degradation even after the CH2Cl2 solution was washed with water. However, subtle structural differences (planar versus partly twisted) led to different crystal packing structures and solid-state magnetic properties.

Original languageEnglish
Pages (from-to)189-199
Number of pages11
JournalChemical Science
Volume8
Issue number1
DOIs
Publication statusPublished - 2017 Jan 1

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Porphyrins
Cations
Diphenylamine
Silica Gel
Dimers
Electrochemical oxidation
Quantum yield
Chromatography
Deterioration
Magnetic properties
Fusion reactions
Fluorescence
phenoxazine
Degradation
Oxidation
Temperature
Crystals
Electrons
Water

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

Cite this

Fukui, N., Cha, W., Shimizu, D., Oh, J., Furukawa, K., Yorimitsu, H., ... Osuka, A. (2017). Highly planar diarylamine-fused porphyrins and their remarkably stable radical cations. Chemical Science, 8(1), 189-199. https://doi.org/10.1039/C6SC02721K
Fukui, Norihito ; Cha, Wonhee ; Shimizu, Daiki ; Oh, Juwon ; Furukawa, Ko ; Yorimitsu, Hideki ; Kim, Dongho ; Osuka, Atsuhiro. / Highly planar diarylamine-fused porphyrins and their remarkably stable radical cations. In: Chemical Science. 2017 ; Vol. 8, No. 1. pp. 189-199.
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Fukui, N, Cha, W, Shimizu, D, Oh, J, Furukawa, K, Yorimitsu, H, Kim, D & Osuka, A 2017, 'Highly planar diarylamine-fused porphyrins and their remarkably stable radical cations', Chemical Science, vol. 8, no. 1, pp. 189-199. https://doi.org/10.1039/C6SC02721K

Highly planar diarylamine-fused porphyrins and their remarkably stable radical cations. / Fukui, Norihito; Cha, Wonhee; Shimizu, Daiki; Oh, Juwon; Furukawa, Ko; Yorimitsu, Hideki; Kim, Dongho; Osuka, Atsuhiro.

In: Chemical Science, Vol. 8, No. 1, 01.01.2017, p. 189-199.

Research output: Contribution to journalArticle

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Fukui N, Cha W, Shimizu D, Oh J, Furukawa K, Yorimitsu H et al. Highly planar diarylamine-fused porphyrins and their remarkably stable radical cations. Chemical Science. 2017 Jan 1;8(1):189-199. https://doi.org/10.1039/C6SC02721K