Issue 9, 2010

Novel carbon-centred reactivity of [(H)C(PPh2Se)2] in the formation of structurally diverse Sn(iv), Te(iv) and Hg(ii) complexes of the triseleno ligand [(Se)C(PPh2Se)2]2–

Abstract

Metathetical reactions between TMEDA·Li[(H)C(PPh2Se)2] and MCl2 (M = Hg, Sn, Te) in a 2 : 1 molar ratio afforded the homoleptic complexes, {M[(H)C(PPh2Se)2]2}, as intermediates which undergo a surprising selenium/hydrogen exchange at the carbon centre to yield the dianionic triseleno ligand in {Mn[(Se)C(PPh2Se)2]2} (n = 1, M = Sn, Te; n = 2, M = Hg).

Graphical abstract: Novel carbon-centred reactivity of [(H)C(PPh2Se)2]− in the formation of structurally diverse Sn(iv), Te(iv) and Hg(ii) complexes of the triseleno ligand [(Se)C(PPh2Se)2]2–

Supplementary files

Article information

Article type
Communication
Submitted
13 Nov. 2009
Accepted
15 Janv. 2010
First published
27 Janv. 2010

Chem. Commun., 2010,46, 1431-1433

Novel carbon-centred reactivity of [(H)C(PPh2Se)2] in the formation of structurally diverse Sn(IV), Te(IV) and Hg(II) complexes of the triseleno ligand [(Se)C(PPh2Se)2]2–

J. Konu and T. Chivers, Chem. Commun., 2010, 46, 1431 DOI: 10.1039/B923910C

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