Monovalent Germanium Radical Stabilized by a Phenalenyl Scaffold

15 November 2022, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

A monovalent (Non-Gomberg type) germanium radical 1 stabilized by phenalenyl-based bidentate ligand was synthe-sized. Because of the high thermal stability originating from spin delocalization over the phenalenyl moiety, it was possi-ble to isolate compound 1 in crystalline form by sublimation at ca. 300 °C. ESR spectra, crystallographic analysis, theo-retical calculations, and reactivities with carbon radicals suggest that the spin of 1 is distributed on the phenalenyl moie-ty, while 1 behaves as a germanium-centered radical in its reactions with C2Cl6, PhSSPh, and p-benzoquinone to form Ge−E (E = Cl, S, O) bonds.

Keywords

Non-Gomberg Radical
Radical
Germanium
Main Group Chemistry
Phenalenyl

Supplementary materials

Title
Description
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Supporting Information
Description
Detailed experimental procedures, characterization of new com-pounds, and computational details.
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CIF
Description
Crystallographic data.
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