Title of article
Generation, isolation, and reactivity of a kinetically stabilized diphosphene anion radical
Author/Authors
Noriyoshi Nagahora، نويسنده , , Takahiro Sasamori، نويسنده , , Yoshinobu Hosoi، نويسنده , , Yukio Furukawa، نويسنده , , Norihiro Tokitoh، نويسنده ,
Issue Information
دوفصلنامه با شماره پیاپی سال 2008
Pages
8
From page
625
To page
632
Abstract
The stable lithium diphosphene anion radical, [Li(dme)3]+[TbtPPTbt]radical dot− (dme: 1,2-dimethoxyethane, Tbt: 2,4,6-tris[bis(trimethylsilyl)methyl]phenyl), was readily synthesized by the one-electron reduction of the corresponding neutral diphosphene (TbtPdouble bond; length as m-dashPTbt). The molecular structure of the diphosphene anion radical was discussed in detail on the basis of its ESR, UV–Vis and Raman spectra, and theoretical calculations. The diphosphene anion radical was found to undergo ready chalcogenation reactions using elemental sulfur and selenium to afford the corresponding thiadiphosphirane and selenadiphosphirane, respectively.
Keywords
Anion radical , UV–vis spectrum , Reduction , Cyclic voltammetry , Diphosphene , ESR spectrum
Journal title
Journal of Organometallic Chemistry
Serial Year
2008
Journal title
Journal of Organometallic Chemistry
Record number
1376315
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