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31.
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The effect of solvents on the extraction of lanthanoids with 18-crown-6 and trichloroacetic acid was investigated for the solvents, 1,1,-dichloroethane, 1,2-dichloroethane, 1,1, 2,2-tetrachloroethane, chloroform, di-2-chloroethyl ether, and methylene chloride. Distribution coefficients (25 °C) normalized to the water solubility (wt./vol.) in the solvents correlated to the polarizability index (*) for La3+, Ce3+, Pr3+, and Nd3+ with r values=0.93,0.93,0.95, and 0.98, respectively. The distribution coefficients for Nd3+ also correlated with the Hildebrand solubility parameter () (r=0.98). These correlations agree with the literature that for large ions, the extraction thermodynamic properties correlate with the polarizability index and Hildebrand solubility parameter. 相似文献
33.
Application of the refined Wiener-Hermite expansion with moderate to high Reynolds numbers Re to homogeneous, isotropic turbulence is presented. The results show a defect to Kolmogorov's five-thirds law, increase in the absolute value of the exponent comparable with many theoretical predictions. Midrange spectra up to fluctuation Reynolds numbers of 108 show little, if any, dependence of the defect on Re, as long as the initial spectra do not deviate too far from their equilibrium states. The renormalization scheme has also been proven to have no effect on the final shape of the spectrum. 相似文献
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Abachi S Derrick M Kooijman P Musgrave B Price LE Repond J Sugano K Blockus D Brabson B Brom J Jung C Ogren H Rust DR Akerlof C Chapman J Errede D Ken MT Meyer DI Neal H Nitz D Thun R Tschirhart R Baringer P Bylsma BG DeBonte R Koltick D Low EH McIlwain RL Miller DH Ng CR Shibata EI 《Physical review D: Particles and fields》1989,40(3):902-905
36.
Stulz E Scott SM Ng YF Bond AD Teat SJ Darling SL Feeder N Sanders JK 《Inorganic chemistry》2003,42(20):6564-6574
The synthesis of linear multiporphyrin arrays with mono- and bisphosphine-substituted porphyrins as ligand donors and ruthenium(II) or rhodium(III) porphyrins as ligand acceptors is described. With appropriate amounts of the building blocks mixed, linear dimeric and trimeric arrays have been synthesized and analyzed by (1)H NMR and (31)P NMR spectroscopy. The Ru/Rh acceptor porphyrins can be located either at the periphery or in the center of the array. Likewise, the monophosphine porphyrins can be positioned at the periphery, thus allowing a high degree of freedom in the overall composition of the arrays. This way, both donor and acceptor porphyrins can act as chain extenders or terminators. One of the trimeric complexes with two nickel and one ruthenium porphyrin has also been analyzed by X-ray crystallography. Attempts have also been made to synthesize higher order arrays by mixing appropriate amounts of the porphyrins; however, from the NMR data it cannot be concluded if monodisperse five, seven, or nine porphyrin arrays are present or if the solutions are composed of a statistical mixture of smaller and larger arrays. 相似文献
37.
Guan X Lin X Kwok WM Du Y Li YL Zhao C Wang D Phillips DL 《The journal of physical chemistry. A》2005,109(6):1247-1256
Ultraviolet photolysis of low concentrations of CH2I2 in methanol solution found that CH2I2 is converted into dimethoxymethane and some H+ and I- products. Picosecond time-resolved resonance Raman (ps-TR3) experiments observed that the isodiiodomethane (CH2I-I) photoproduct decayed faster as the concentration of methanol increases, suggesting that isodiiodomethane is reacting with methanol. Ab initio calculations indicate isodiiodomethane is able to react with methanol via an O-H insertion/HI elimination to form an iodoether (ICH2-O-CH3) and HI products. The iodoether can then further react via another O-H insertion/HI elimination reaction to form the dimethoxymethane (CH3-O-CH2-O-CH3) observed in the photochemistry experiments. A reaction mechanism consistent with these experimental and theoretical observations is proposed. 相似文献
38.
The ultraviolet photolysis of low concentrations of CH(2)XI (X = Cl, Br, I) were investigated in water and saltwater solutions by photochemistry and picosecond time-resolved resonance Raman spectroscopy. Photolysis in both kinds of solutions formed mostly CH(2)(OH)(2) and HI and HX products. However, photolysis of the CH(2)XI molecules in saltwater resulted in production of some CH(2)XCl products not observed in aqueous solutions without salt present. The appearance of these new products in saltwater solutions is accompanied by a decrease in the amount of CH(2)(OH)(2), HI, and HX products compared to photolysis in aqueous solutions without salt present. The possible implications for photolysis of CH(2)XI and other polyhalomethanes in seawater and other salt aqueous environments compared to nonsaltwater solvated environments is briefly discussed. 相似文献
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Abachi S Akerlof C Baringer P Blockus D Brabson B Brom J Bylsma BG Chapman J Cork B DeBonte R Derrick M Errede D Gan KK Jung C Ken MT Koltick D Kooijman P Loeffler FJ Loos JS Low EH McIlwain RL Meyer DI Miller DH Musgrave B Neal H Ng CR Nitz D Ogren H Paik HW Price LE Rangan LK Repond J Rust DR Shibata EI Sugano K Thun R Tschirhart R 《Physical review letters》1987,59(22):2519-2522