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Microsolvation of the [Ni(acac)(tmen)]+ complex by a series of aliphatic n-alcohols (Solv) has been studied in ClCH2CH2Cl solutions by spectrophotometry. Based on the changes in the electronic spectrum of the afore-mentioned complex, observed under the influence of any alcohol, the equilibrium constants for the formation of the [Ni(acac)(tmen)Solv]+ and [Ni(acac)(tmen)Solv2]+ species have been computed according to the algorithm presented in this work. It was found that, in all the systems studied, the stability of five-coordinated [Ni(acac)(tmen)Solv]+ is higher than that of octahedral [Ni(acac)(tmen)Solv2]+. The resulting values are discussed in terms of the Lewis basicity of alcohols.  相似文献   
2.
The visible absorption spectra of CoCl2 in binary mixtures of acetone, dmf, dma and dmso with H2O show the existence of configuration equilibria between tetrahedral (T) and octahedral (O) species. Linear correlations between the values of log K (K = [O]/[T]) and the mole fraction of H2O, w, have been observed in all the systems under study; their slopes decrease linearly with an increase of the donor number, DN, of the organic component of the mixture. The formation of octahedral species is enthalpy favoured but entropy disfavoured. It was found that both H and S values change linearly with w and the slopes of these relationships depend clearly on the DN values.  相似文献   
3.
The scavening of OH· radicals by 2- and 6-mercaptopurines (2-MP and 6-MP) and purine was studied spectrophotometrically using the competition method. The air-saturated aqueous solutions of these compounds in the presence of p-nitroso-N,N-dimethylaniline (NDMA) were -irradiated (-source—60Co). The absolute rate constants for the scavening of OH· radicals by 2-MP and 6-MP were calculated. Main product as produced by irradiation of 2-MP was identified.  相似文献   
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