Journal
ORGANOMETALLICS
Volume 34, Issue 20, Pages 4932-4940Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.organomet.5b00448
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- ESF DoRa T6 Development of international cooperation networks by supporting the mobility of Estonian doctoral students
- Vetenskapsradet
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The (PNP)IrH3 (2,6-bis(diisopropylphosp-hinomethyl)pyridine iridium trihydride) complex by Nozaki is a highly active and selective catalyst for CO2 hydrogenation to formic acid in aqueous KOH. Previous theoretical investigations found that regeneration of the catalyst is the rate-determining step in this reaction. In the current article we present results from a computational study using density func- theory in order to consider the possibility of sequential insertion of two CO2 molecules in two Ir-H bonds before the reaction with hydrogen. We found that insertion of a second CO2 molecule is indeed possible; moreover, this sequential insertion allows formation of a more electrophilic iridium mono-hydride intermediate, and thereby the process of H-2 cleavage is facilitated. In addition, we considered the influence of ligands coplanar with the PNP ligand on the energy of CO2 insertion into the (PNP)IrH2X complex and found that sigma- and pi-donating ligands promote the reaction.
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