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Antimony Complexes for Electrocatalysis: Activity of a Main-Group Element in Proton Reduction.
Jiang, Jianbing; Materna, Kelly L; Hedström, Svante; Yang, Ke R; Crabtree, Robert H; Batista, Victor S; Brudvig, Gary W.
Afiliação
  • Jiang J; Department of Chemistry, Yale University, New Haven, CT, 06520, USA.
  • Materna KL; Energy Sciences Institute, Yale University, West Haven, CT, 06516, USA.
  • Hedström S; Department of Chemistry, Yale University, New Haven, CT, 06520, USA.
  • Yang KR; Energy Sciences Institute, Yale University, West Haven, CT, 06516, USA.
  • Crabtree RH; Department of Chemistry, Yale University, New Haven, CT, 06520, USA.
  • Batista VS; Energy Sciences Institute, Yale University, West Haven, CT, 06516, USA.
  • Brudvig GW; Department of Chemistry, Yale University, New Haven, CT, 06520, USA.
Angew Chem Int Ed Engl ; 56(31): 9111-9115, 2017 07 24.
Article em En | MEDLINE | ID: mdl-28628943
Main-group complexes are shown to be viable electrocatalysts for the H2 -evolution reaction (HER) from acid. A series of antimony porphyrins with varying axial ligands were synthesized for electrocatalysis applications. The proton-reduction catalytic properties of TPSb(OH)2 (TP=5,10,15,20-tetra(p-tolyl)porphyrin) with two axial hydroxy ligands were studied in detail, demonstrating catalytic H2 production. Experiments, in conjunction with quantum chemistry calculations, show that the catalytic cycle is driven via the redox activity of both the porphyrin ligand and the Sb center. This study brings insight into main group catalysis and the role of redox-active ligands during catalysis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article