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931.
The reaction of a fluorinated iridium complex with cerium(IV) and organic reducing agents generates an intense emission with a significant hypsochromic shift compared to contemporary chemically-initiated luminescence from metal complexes. 相似文献
932.
Simon M. Clark Raymond L. Jones C. Michael B. Henderson Berwyn Varney 《Journal of Physics and Chemistry of Solids》2008,69(9):2168-2171
An apparatus for measuring the complex impedance of samples with high impedances is described. Complex impedance spectra were collected from a range of borosilicate glasses of composition (B2O3)4(Li2O)(LiBr)x(NaBr)1−x at pressures and temperatures ranging from 1 to 5 GPa and 350 to 450 °C, respectively. These data were used to determine AC conductivities and activation energies in order to test the Modified Random Network model of glass structure. Our results are in line with the predictions of this theory. 相似文献
933.
Cedrick O'Shaughnessy Grant S. Henderson Benjamin J. A. Moulton Lucia Zuin Daniel R. Neuville 《Journal of synchrotron radiation》2018,25(2):543-551
The first comprehensive Li K‐edge XANES study of a varied suite of Li‐bearing minerals is presented. Drastic changes in the bonding environment for lithium are demonstrated and this can be monitored using the position and intensity of the main Li K‐absorption edge. The complex silicates confirm the assignment of the absorption edge to be a convolution of triply degenerate p‐like states as previously proposed for simple lithium compounds. The Li K‐edge position depends on the electronegativity of the element to which it is bound. The intensity of the first peak varies depending on the existence of a 2p electron and can be used to evaluate the degree of ionicity of the bond. The presence of a 2p electron results in a weak first‐peak intensity. The maximum intensity of the absorption edge shifts to lower energy with increasing SiO2 content for the lithium aluminosilicate minerals. The bond length distortion of the lithium aluminosilicates decreases with increasing SiO2 content, thus increased distortion leads to an increase in edge energy which measures lithium's electron affinity. 相似文献
934.
935.
Jefferson L. M. A. Gomes Nlio Henderson Marisa C. G. Rocha 《Macromolecular theory and simulations》2001,10(9):816-826
This work presents the vapor–liquid equilibrium calculations in an isothermal flash, applied to polymer solutions, using the Peng–Robinson cubic equation of state modified by Stryjek–Vera, and the mixing rule introduced by Wong–Sandler. This rule allows combining the rigid lattice thermodynamic model of Flory–Huggins to the Peng–Robinson–Stryjek–Vera equation of state. As the Gibbs free energy must be minimum in the equilibrium state, a stochastic optimization method, the simulated annealing algorithm, was used to find out the extreme of this thermodynamic potential. 相似文献
936.