Interactions of NO and CO with Pd and Pt atoms

Gregory W. Smith, Emily A. Carter

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100 Scopus citations

Abstract

We report ab initio generalized valence bond and correlation-consistent configuration interaction studies of CO and NO interacting with Pd and Pt atoms. We find dramatically different bonding mechanisms for the two ligands, which are easily understood in terms of changes in the electronic structure of the metal and the ligand. CO bonds to both Pd and Pt by a σ donor/π back-bonding mechanism, yielding linear geometries. Our calculations predict that the ground (1Σ+) state of PdCO is bound by 27 kcal/mol, while the ground (1Σ+) state of PtCO is bound by only 18.5 kcal/mol. By contrast, PdNO and PtNO are both bent, with the dominant bonding involving a covalent σ bond between a singly occupied metal dσ orbital and the singly occupied NO 2π* orbital. While the ground (2A′) state of PtNO is strongly bound [De(Pt-NO) ∼ 20 kcal/mol], NO binds very weakly to Pd [De(Pd-NO) ≤ 4 kcal/mol]. Linear excited states (2Σ+ and 2Π) of PtNO and PdNO are predicted to be only weakly bound or unbound. However, corresponding linear cationic states (1Σ+ and 3Π) are strongly bound, but the cationic bent (1A′) states are still the ground states of PtNO+ and PdNO+. These stark contrasts, in which NO binds strongly to Pt but weakly to Pd while CO binds much more strongly to Pd, are due to the preference for closed-shell species to bind strongly to other closed-shell species (e.g., CO to Pd) and for radicals to bind strongly to other radicals (e.g., NO to Pt).

Original languageEnglish (US)
Pages (from-to)2327-2339
Number of pages13
JournalJournal of physical chemistry
Volume95
Issue number6
DOIs
StatePublished - Jan 1 1991
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Engineering(all)
  • Physical and Theoretical Chemistry

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