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Redox-active ligand based Mn(I)-catalyst for hydrosilylative ester reduction.

Soumi ChakrabortyArpan DasSwadhin K Mandal
Published in: Chemical communications (Cambridge, England) (2021)
Herein a Mn(I) catalyst bearing a redox-active phenalenyl (PLY) based ligand is reported for the efficient hydrosilylation of esters to alcohols using the inexpensive silane source polymethylhydrosiloxane (PMHS) under mild conditions. Mechanistic investigations suggest a strong ligand-metal cooperation where a ligand-based single electron transfer (SET) process initiates the reaction through Si-H bond activation.
Keyphrases
  • electron transfer
  • room temperature
  • metal organic framework
  • ionic liquid
  • highly efficient
  • reduced graphene oxide
  • carbon dioxide