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Delocalized Radicals

T. Kubo, Y. Katada, A. Shimizu, Y. Hirao, K. Sato, T. Takui, M. Uruichi, K. Yakushi, R. C. Haddon

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Abstract

Significance The authors synthesized the hy­drocarbon radicals stabilized predominantly by a thermodynamic factor. The large extent of de­localization of an unpaired electron suppresses σ-bond formation between the radicals. Instead, the radical forms a π-dimer in the solid state via multicenter bonding of the unpaired electrons.

About this research paper

What this paper is about

Significance The authors synthesized the hy­drocarbon radicals stabilized predominantly by a thermodynamic factor. The large extent of de­localization of an unpaired electron suppresses σ-bond formation between the radicals. Instead, the radical forms a π-dimer in the solid state via multicenter bonding of the unpaired electrons.

Why it matters

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Method / approach

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Available abstract

Significance The authors synthesized the hy­drocarbon radicals stabilized predominantly by a thermodynamic factor. The large extent of de­localization of an unpaired electron suppresses σ-bond formation between the radicals. Instead, the radical forms a π-dimer in the solid state via multicenter bonding of the unpaired electrons.

Key concepts: Unpaired electron, Radical, Chemistry, Delocalized electron, Dimer, Electron delocalization, Photochemistry, Solid-state

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