Issue 44, 2009

Synthesis of a germanium analogue of a dithiocarboxylic acid anhydride from the Ge(i) pyridyl-1-azaallyl dimer

Abstract

The reaction of pyridyl-1-azaallyl germanium(II) chloride RGeCl (1) [R = {N(SiMe3)C(Ph)C(SiMe3)(C5H4N-2)}] with lithium metal afforded the dimeric germanium(I) compound [(RGe)2] (2); compound 2 reacts with an excess of elemental sulfur to afford the novel germanium analogue of a dithiocarboxylic acid anhydride [{Ge(S)R}2S] (4) via the insertion of elemental sulfur into the Ge(I)–Ge(I) bond followed by the oxidative-addition of elemental sulfur to the germanium(II) centres.

Graphical abstract: Synthesis of a germanium analogue of a dithiocarboxylic acid anhydride from the Ge(i) pyridyl-1-azaallyl dimer

Supplementary files

Article information

Article type
Communication
Submitted
07 Aug 2009
Accepted
14 Sep 2009
First published
28 Sep 2009

Chem. Commun., 2009, 6822-6824

Synthesis of a germanium analogue of a dithiocarboxylic acid anhydride from the Ge(I) pyridyl-1-azaallyl dimer

W. Leung, W. Chiu, K. Chong and T. C. W. Mak, Chem. Commun., 2009, 6822 DOI: 10.1039/B916326C

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