期刊文献+

Decavanadate-based Transition Metal Hybrids as Bifunctional Catalysts for Sulfide Oxidation and C-C Bond Construction 被引量:1

原文传递
导出
摘要 The development of bifunctional catalysts has drawn much attention in realizing efficient and feasible catalytic systems to meet the diverse dema nd of pote ntial industrial applications.Desig n of stable and powerful bifun ctional catalysts for various catalysis systems is highly desirable yet largely unmet.Here,three kinds of decavanadate-based transition metal hybrids(DTMH)(i.e.,Co-DTMH,Ni-DTMH and Ag-DTMH)have been successfully synthesized through a pH tuning strategy and further characterized.Specifically,the rare M05N six-coordinated transition metal coordination modes have been detected in Co-DTMH and Ni-DTMH,while Ag atoms in Ag-DTMH exhibited three-and five-coordinated geometries with the tuning of specially selected imidazole ligands.Thus-obtained clusters can serve as powerful bifunctional catalysts for both sulfide oxidation and C-C bond construction.Remarkably,Ag-DTMH dem on st rated excellent heteroge ne ous bifunctional catalytic properties in the selective oxidati on of sulfides and construction of C-C bond(yields up to 99%),which enable successful recycling for three cycles with remained catalytic activities and structure stability.The newly designed decavanadate-based transition metal hybrids with bifunctional property hold high promise in the practical applications like continuous catalysis or flow bed reactions.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2021年第9期2495-2503,共9页 中国化学(英文版)
基金 supported by the National Natural Science Foundation of China(Nos.21871125 and 21901122) the Natural Science Foundation of Shandong Province,China(Nos.ZR2019MB043 and ZR2019QB022) the Construction Project of Quality Curriculum for Postgraduate Education of Shandong Province(No.SDYKC19057) the Natural Science Research of Jiangsu Higher Education Institutions of China(No.19KJB150011) Project funded by China Postdoctoral Science Foundation(No.2019M651873).
  • 相关文献

参考文献8

二级参考文献26

共引文献20

同被引文献6

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部