Electronic structure and Mössbauer hyperfine interactions of Au(I) compounds

Diana Guenzburger*, D. E. Ellis

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

36 Scopus citations

Abstract

The electronic structure of the linear Au(1) complexes (AuX2)-1, where X=CN,Cl,andF has been studied in the self-consistent one-electron statistical exchange model. The relative importance of gold 5d, 6s, and 6p states in chemical bonding and for hyperfine interactions is examined, using linear-combination-of-atomic-orbitals decomposition of the molecular eigenstates. The variation of the isomer shift and quadrupole splitting of Au197 with covalency is studied theoretically. The effect of pressure on these hyperfine interactions for K[Au(CN)2] is investigated by considering different interatomic distances. In this latter case, the main discrepancies with respect to experiment found are believed to arise from bonding with exterior atoms. Relativistic effects are briefly explored by comparison of Dirac-Slater relativistic and nonrelativistic results for the cyanide anion.

Original languageEnglish (US)
Pages (from-to)4203-4214
Number of pages12
JournalPhysical Review B
Volume22
Issue number9
DOIs
StatePublished - Jan 1 1980

ASJC Scopus subject areas

  • Condensed Matter Physics

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