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Electrochemical Transition Metal Hydride Catalysis

  • Xinyi Wang
  • , Depeng Duan
  • , Lu Song*
  • , Niankai Fu*
  • *Corresponding author for this work
  • CAS - Institute of Chemistry
  • University of Chinese Academy of Sciences
  • Beihang University

Research output: Contribution to journalReview articlepeer-review

Abstract

Transition metal hydride catalysis has emerged as a versatile tool for developing new bond-disconnection strategies in synthetic chemistry. Conventional approaches to generate the key transition metal hydride species, however, remain constrained by their dependence on the use of stoichiometric hydride donors (e.g., hydrosilanes, borohydrides) and frequently require relatively complex reaction conditions. As a complementary and attractive alternative, electrochemically generated transition metal hydrides have recently been demonstrated to be catalytically effective intermediates for achieving similar synthetic purposes, employing electrons as the redox agents in a more practical and sustainable manner. This Concept introduces electrochemical transition metal hydride catalysis in the alkene functionalization and the synthesis of alkenes from alkyl radicals, providing an overview of recent advances, current limitations, and prospective future directions in this emerging field.

Original languageEnglish
Article numbere00348
JournalChemCatChem
Volume17
Issue number14
DOIs
StatePublished - Jul 2025

Keywords

  • Alkene
  • Electrochemistry
  • Hydrogen atom transfer
  • Metal hydride
  • Radical

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