首页    期刊浏览 2024年12月03日 星期二
登录注册

文章基本信息

  • 标题:Proton–hydride tautomerism in hydrogen evolution catalysis
  • 本地全文:下载
  • 作者:Luis M. Aguirre Quintana ; Samantha I. Johnson ; Sydney L. Corona
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2016
  • 卷号:113
  • 期号:23
  • 页码:6409-6414
  • DOI:10.1073/pnas.1606018113
  • 语种:English
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:Efficient generation of hydrogen from renewable resources requires development of catalysts that avoid deep wells and high barriers. Information about the energy landscape for H2 production can be obtained by chemical characterization of catalytic intermediates, but few have been observed to date. We have isolated and characterized a key intermediate in 2e– + 2H+ → H2 catalysis. This intermediate, obtained by treatment of Cp*Rh(bpy) (Cp*, η5-pentamethylcyclopentadienyl; bpy, κ2-2,2′-bipyridyl) with acid, is not a hydride species but rather, bears [η4-Cp*H] as a ligand. Delivery of a second proton to this species leads to evolution of H2 and reformation of η5-Cp* bound to rhodium(III). With suitable choices of acids and bases, the Cp*Rh(bpy) complex catalyzes facile and reversible interconversion of H+ and H2.
  • 关键词:rhodium ; pentamethylcyclopentadienyl ; catalysis ; proton reduction ; hydrogen evolution
国家哲学社会科学文献中心版权所有