51V NMR studies of crystalline monovalent and divalent metal metavanadates

Satoshi Hayakawa, Toshinobu Yoko, Sumio Sakka

Research output: Contribution to journalArticlepeer-review

33 Citations (Scopus)

Abstract

51V static and magic-angle spinning (MAS) NMR spectra of crystalline monovalent metal metavanadates LiVO3, α- and βNaVO3, KVO3, CsVO3, β-AgVO3, and NH4VO3 and divalent metal metavanadates M(VO3)2 (M = Mg, Ca, Sr, Ba, Zn, Pb) have been measured in order to establish the relationships between the various NMR parameters, such as isotropic chemical shift, δiso, chemical shift anisotropy, |Δ;δ|, the asymmetry parameter, η, and the crystallographic parameters. When the structural units are the same, in this case VO4 tetrahedra or VO5 trigonal bipyramids, the δiso decrease almost linearly with decreasing average V-O bond length, independent of the polymerization degree and linkage mode of the VOn polyhedra. |Δ;δ|, increases with the polymerization degree and the degree of the structural distortion of the VOn polyhedron. It is found possible to predict the structural unit and the polymerization degree on the basis of the relation between |Δ;δ| and η.

Original languageEnglish
Pages (from-to)329-339
Number of pages11
JournalJournal of Solid State Chemistry
Volume112
Issue number2
DOIs
Publication statusPublished - Oct 1994
Externally publishedYes

ASJC Scopus subject areas

  • Electronic, Optical and Magnetic Materials
  • Ceramics and Composites
  • Condensed Matter Physics
  • Physical and Theoretical Chemistry
  • Inorganic Chemistry
  • Materials Chemistry

Fingerprint Dive into the research topics of '<sup>51</sup>V NMR studies of crystalline monovalent and divalent metal metavanadates'. Together they form a unique fingerprint.

Cite this