Beilstein Journal of Organic Chemistry (Aug 2024)

Radical reactivity of antiaromatic Ni(II) norcorroles with azo radical initiators

  • Siham Asyiqin Shafie,
  • Ryo Nozawa,
  • Hideaki Takano,
  • Hiroshi Shinokubo

DOI
https://doi.org/10.3762/bjoc.20.172
Journal volume & issue
Vol. 20, no. 1
pp. 1967 – 1972

Abstract

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Norcorrole is a stable 16π-antiaromatic porphyrinoid that exhibits characteristic reactivities and physical properties. Here, we disclose the reaction of Ni(II) norcorroles with alkyl radicals derived from azo radical initiators. The radical selectively attacked the distal α-position relative to the meso-position to construct a nonaromatic bowl-shaped structure. The photophysical and electrochemical properties of the obtained radical adducts were compared to those of the parent Ni(II) norcorrole. The radical reactivity of Ni(II) norcorroles was investigated by density functional theory (DFT) calculations.

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