Electron spin lattice relaxation of V(IV) complexes in glassy solutions between 15 and 70 K

Alistair J. Fielding, Dong Bin Back, Michael Engler, Bharat Baruah, Debbie C. Crans, Gareth R. Eaton, Sandra S. Eaton

    Research output: Chapter in Book/Conference proceedingChapter

    Abstract

    Electron spin lattice relaxation rates for four vanadium(IV) complexes: bis(acetyIacetonate)oxovanadium(IV), (VO-(acac) 2), 1; bis(maltolato)oxovanadium(IV), (VO(maltol)2), 2; Cesium N,N′- ethylenebis(salicylideneiminato-5′-sulfonato)oxovanadium(IV), Cs 2[VO(salen-SO 3)(H 2O)], 3; and bis(N-hydroxyiminodiacetato)oxovanadium(IV), (Ca[V(hida) 2]), 4; in 1:1 watenglycerol glasses were measured by long-pulse saturation recovery at X-band. Although these complexes have coordination spheres that vary from O 5 to N 4O and N 2O 6, the relaxation rates differ by factors of only about 2 at 15 K and 4 at 70 K. Relaxation rates for 4, which does not contain an oxo group, are very similar to those for oxo-containing complexes. At 70 K relaxation rates decrease in the order aquo VO 2+ > VO(acac) 2 ∼ VO(maltol) 2 > [V(hida) 2] 2- > [VO(salen-SO 3) (H 2O)] 2- > vanadyl porphyrin. This order correlates with decreasing flexibility of the ligands and coordination sphere. The temperature dependence of spin lattice relaxation rates was analyzed in terms of contributions from the direct process, the Raman process, and local modes. © 2007 American Chemical Society.
    Original languageEnglish
    Title of host publicationACS Symposium Series|ACS Symp. Ser.
    Subtitle of host publicationVanadium: The Versatile Metal
    PublisherAmerican Chemical Society
    Pages364-375
    Number of pages11
    Volume974
    DOIs
    Publication statusPublished - 2007

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