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 language | English |
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Title of host publication | ACS Symposium Series|ACS Symp. Ser. |
Subtitle of host publication | Vanadium: The Versatile Metal |
Publisher | American Chemical Society |
Pages | 364-375 |
Number of pages | 11 |
Volume | 974 |
DOIs | |
Publication status | Published - 2007 |