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Updated: May 5, 2026
![The Synthesis of [Sn10SiSiMe334]2- Using a Metastable SnI Halide Solution Synthesized via a Co-condensation Technique](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F54498.jpg&w=3840&q=50)
The Synthesis of [Sn10SiSiMe334]2- Using a Metastable SnI Halide Solution Synthesized via a Co-condensation Technique
Published on: November 28, 2016
Polyoxometalate-catalyzed insertion of oxygen from O(2) into tin-alkyl bonds
Alexander M Khenkin1, Irena Efremenko, Jan M L Martin
1Department of Organic Chemistry, Weizmann Institute of Science , Rehovot, Israel 76100.
Abstract:
The polyoxometalate H5PV2Mo10O40 mediates the insertion of an oxygen atom from H5PV2Mo10O40 into the tin-carbon bond of n-Bu4Sn through its activation by electron transfer to yield 1-butanol and (n-Bu3Sn)2O. The reaction is initiated by electron transfer from n-Bu4Sn to H5PV(V)2Mo10O40 to yield the ion pair n-Bu4Sn(•+)-H5PV(IV)V(V)Mo10O40. The H5PV(IV)V(V)Mo10O40 moiety was identified by UV-vis and EPR. DFT calculations show that n-Bu4Sn(•+)-H5PV(IV)V(V)Mo10O40 is relatively unstable and forms more stable Bu(+) and Bu3Sn(+) cations coordinated to the polyoxometalate, which were also identified by ESI-MS. Products are released at higher temperatures. In the presence of molecular oxygen as the terminal oxidant the reaction is catalytic.
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