Bound triplet pairs in the highest spin states of coinage metal clusters

David Danovich, Sason Shaik*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

The work discusses bonding in coinage metal clusters, n+1M n (M = Cu, Ag, Au), that have maximum spin without a single electron pair. It is shown that the bonding energy per atom, De/n, exhibits a strong nonadditive behavior; it grows rapidly with the cluster size and converges to values as large as 16-19 kcal/mol for Au and Cu. A valence bond (VB) analysis shows that this no-pair ferromagnetic bonding arises from bound triplet electron pairs that spread over all the close neighbors of a given atom in the clusters. The bound triplet pair owes its stabilization to the resonance energy provided by the mixing of the local ionic configurations, 3M(↑ ↑)-M+ and M + 3M(↑ ↑)-, and by the various excited covalent configurations (involving pz and dz2 atomic orbitals) into the fundamental covalent structure 3(M↑ ↑M) with a s1s1 electronic configuration. The VB model shows that a weak interaction in the dimer can become a remarkably strong binding force that holds together monovalent atoms without a single electron pair.

Original languageEnglish
Pages (from-to)1479-1489
Number of pages11
JournalJournal of Chemical Theory and Computation
Volume6
Issue number5
DOIs
StatePublished - 11 May 2010

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