Carbon dioxide reduction by pincer rhodium η2-dihydrogen complexes

Hydrogen-binding modes and mechanistic studies by density functional theory calculations

Kuo Wei Huang, Joseph H. Han, Charles B. Musgrave, Etsuko Fujita

Research output: Contribution to journalArticle

48 Citations (Scopus)

Abstract

Density functional theory (DFT) calculations using the KMLYP method on a series of pincer PCP-rhodium dihydrogen complexes have been employed to model and examine the proposed mechanisms for the pincer PCP-rhodium complexes mediated hydrogenation of carbon dioxide (CO2). The relative energies of dihydrogen rotamers and dihydride isomers were evaluated together with T1 values to determine the molecular structures of these complexes. We have investigated possible pathways for the CO2 reduction processes involving the formation of rhodium dihydride species. Although the dihydrogen complexes are more stable than the corresponding dihydride isomers, the reduction of CO2 has to proceed through the dihydride structures.

Original languageEnglish
Pages (from-to)508-513
Number of pages6
JournalOrganometallics
Volume26
Issue number3
DOIs
Publication statusPublished - Jan 29 2007

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dihydrides
Rhodium
rhodium
Carbon Dioxide
Density functional theory
carbon dioxide
Hydrogen
density functional theory
Isomers
hydrogen
isomers
Molecular structure
Hydrogenation
hydrogenation
molecular structure
energy

ASJC Scopus subject areas

  • Inorganic Chemistry
  • Organic Chemistry

Cite this

Carbon dioxide reduction by pincer rhodium η2-dihydrogen complexes : Hydrogen-binding modes and mechanistic studies by density functional theory calculations. / Huang, Kuo Wei; Han, Joseph H.; Musgrave, Charles B.; Fujita, Etsuko.

In: Organometallics, Vol. 26, No. 3, 29.01.2007, p. 508-513.

Research output: Contribution to journalArticle

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