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Electron Spin Lattice Relaxation of V(IV) Complexes in Glassy Solutions between 15 and 70 K

机译:玻璃溶液中的v(iv)复合物的电子旋转晶格弛豫在15到70 k之间

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Electron spin lattice relaxation rates for four vanadium(IV) complexes: bis(acetylacetonate)oxovanadium(IV), (VO-(acac)2), 1; bis(maltolato)oxovanadium(IV), (VO(maltol)2), 2; Cesium N,N'-ethylenebis(salicylideneiminato-5'-sulfonato)-oxovanadium(IV), Cs2[VO(salen-SO3)(H2O)], 3; and bis(N-hydroxyiminodiacetato)oxovanadium(IV), (Ca[V(hida)2]), 4; in 1:1 water: glycerol glasses were measured by long-pulse saturation recovery at X-band Although these complexes have coordination spheres that vary from O5 to N4O and N2O6, 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 VO2+ > VO(acac)2 -VO(maltol)2 > [V(hida)2]2" > [VO(salen-SO3) (H2O)]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.
机译:四种钒(IV)配合物的电子旋转晶格松弛率:双(乙酰丙酮)氧化钒(IV),(VO-(ACAC)2),1;双(麦芽糖丙醇)氧化钒(IV),(VO(马来尔)2),2;铯N,N'-乙烯比(SalicylideneIminato-5'-磺砜) - 脱氧铵(IV),Cs2 [VO(Salen-So3)(H 2 O)],3;和双(N-羟基咪唑乙酯)氧化钒(IV),(Ca [V(HIDA)2]),4;在1:1水中:通过在X频带的长脉冲饱和恢复来测量甘油玻璃,尽管这些配合物具有从O5到N4O和N2O6变化的协调球,但是弛豫率因仅为15 k和4时的因素而异。在70 k.4的弛豫速率下,不含氧代组的4个,与含氧氧气的络合物在70k弛豫率下降的含量氧气的复合物的弛豫速率非常相似,订单Aquo Vo2 +> vo(ACAC)2 -VO(Maltol)2 > [V(HIDA)2] 2“> [VO(Salen-SO3)(H2O)] 2”>甲酰卟啉卟啉此顺序与降低配体和配体球的柔韧性相关。根据直接过程,拉曼工艺和局部模式的贡献,分析了旋转晶格松弛率的温度依赖性。

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