{V6} Ring Sandwiched Polyoxoniobate as Molecular Electrocatalyst for Oxidant‐Free Synthesis of Sulfoxides

Author:

Zhen Ni1,Dong Jing2,Lin Zhengguo3,Li Zhen14,Liu Chengpeng1,Li Xiaoxia1,Geng Weijie1,Chi Yingnan1ORCID,Hu Changwen1

Affiliation:

1. School of Chemistry and Chemical Engineering Beijing Institute of Technology Fangshan District Beijing 102488 P. R. China

2. College of Chemistry and Materials Engineering Beijing Technology and Business University Haidian District Beijing 100048 P. R. China

3. College of Chemistry and Materials Science Hebei Normal University Shijiazhuang Hebei 050024 P. R. China

4. School of Chemistry and Chemical Engineering Liaocheng University Liaocheng Shandong 252000 P. R. China

Abstract

AbstractElectrocatalytic oxidation of organic molecules to value‐added chemicals has attracted recent attention. Although a series of transition metal based electrocatalytic materials have been developed, the lack of precise structure information generates great challenges in understanding the catalytic mechanism at a molecular level. Herein, we present the synthesis and characterization of a molecular electrocatalyst, Na2K6H14[(VO)6(α‐TeNb9O33)2] ⋅ 31H2O ⋅ 2.5 C2H8N2 (abbreviated as V6(TeNb9)2), where a reduced {V6} ring is sandwiched by two trivacant Keggin‐type {α‐TeNb9O33}. V6(TeNb9)2 as heterogeneous electrocatalyst can selectively convert 95 % of thioanisole to sulfoxide with the Faraday efficiency up to 98 %. Notably, the important role of the embedded {V6} ring in the electrocatalytic oxidation was illustrated by comparing with {Nb6} ring sandwiched catalyst, Na5K7H4[(NbO)6(α‐TeNb9O33)2] ⋅ 17H2O (abbreviated as Nb6(TeNb9)2). Mechanism studies reveal that during the electrocatalytic oxidation process water is the only oxygen source and a key intermediate PhCH3S+⋅ is involved.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

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