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排序方式: 共有333条查询结果,搜索用时 31 毫秒
1.
František Toman Ludvík Beneš 《Journal of inclusion phenomena and macrocyclic chemistry》2007,59(3-4):231-236
Differential molar adsorption enthalpies (DMAE) were determined by gas chromatographic measurements of specific retention
volume of vapors on the surface of two forms of Mg–Al hydrotalcite. A linear dependence of the DMAE on the number of the carbon
atoms in hydrocarbons was observed for both form of hydrotalcite. The dependence of the differential molar adsorption enthalpies
on the number of chlorine atoms in organic molecules is discussed. A linear dependence of DMAE on the molecular weight of
chloroderivatives of methane and ethylene on the basic form in an order monochloromethane < dichloromethane < trichloromethane
or vinylidene chloride < 1,1-dichloroethylene < trichloroethylene was found. 相似文献
2.
Gyula Bene 《Central European Journal of Physics》2003,1(2):332-343
An “almost diagonal” reduced density matrix (in coordinate representation) is usually a result of environment induced decherence
and is considered the sign of classical behavior. We show that the proton of a ground state hydrogen atom can indeed possess
such a density matrix. This example demonstrates that the “almost diagonal” structure may be derived from an interaction with
a low number of degrees of freedom which play the role of the environment. We also show that decoherence effects in our example
can only be observed if the interaction with the measuring device is significantly faster than the interaction with the environment
(the electron). In the opposite case, when the interaction with the environment is significant during the measurement process,
coherence is maintained. Finally, we propose a neutron scattering experiment on cold He atoms to observe decoherence which
shows up as an additional positive contribution to the differential scattering cross section. This contribution is inversely
proportional to the bombarding energy. 相似文献
3.
4.
Klára Melánová Ludvík Bene? Vítzslav Zima Jan Svoboda 《Journal of inclusion phenomena and macrocyclic chemistry》2005,51(1):97-101
The intercalates of Naphthol Yellow S, Tropaeolin 000, and Tropaeolin 00 were prepared by heating [Zn0.67Al0.33(OH)2](CO3)0.165 · 0.5H2O with acidic forms of the dye solutions in an open reaction vessel. The intercalates were characterized by chemical and thermal analysis, X-ray powder diffraction and UV–VIS spectroscopy. A possible arrangement of the dye molecules in the intercalates was suggested on the basis of their chemical compositions and interlayer distances, by taking into account van der Waals dimensions of the guest molecules and by assuming that the structure of the host layers is not changed during the intercalation process. 相似文献
5.
Janet E. Del Bene 《Chemical physics》1979,40(3):329-335
Ab initio SCF calculations have been performed to determine the relative lithium ion affinities of the carbonyl bases R2CO and the structures of the complexes R2COLi+. The predicted order of lithium ion affinity for the bases R2CO with respect to R is NH2 > CH3 > OH> H> F. Except for (OH)2COLi+ which has Ca, symmetry, the complexes R2COLi+ have C2v symmetry, with the lithium ion located on the symmetry axis near the oxygen. The major structural changes in the intramolecular coordinates of the bases which occur upon lithium ion complexation include an increase in the carbonyl C---O bond length, a decrease in the length of the bond from the carbonyl carbon to the substituent atom X, and an increase in the X---C---X angle at the carbonyl carbon. The energetic, structural, and electronic properties of the complexes indicate that the interaction between the lithium ion and a carbonyl base is predominantly an ion-dipole attraction rather than a covalent interaction. 相似文献
6.
Klára Melánová Ludvík Beneš Vítězslav Zima Jan Svoboda Miroslava Trchová Jiří Dybal 《Journal of inclusion phenomena and macrocyclic chemistry》2007,58(1-2):95-101
Intercalation compounds of α-Zr(HPO4)2 · H2O with 1,2-alkanediols (from C3 to C16) have been prepared by replacing 1-propanol in α-Zr(HPO4)2 · 2C3H7OH with the desired 1,2-alkanediols by a treatment in a microwave field. It was found that the intercalates contain 1.5 molecules
of diol per formula unit. The diol molecules are placed between the host layers in a bimolecular way with their aliphatic
chains tilted at an angle of 51°. The diol molecules are anchored in the interlayer space by H-bonds. A mixed intercalate,
containing 1,2-butanediol and 1,2-decanediol in a roughly equimolar ratio, is formed when the α-Zr(HPO4)2 · 2C3H7OH intercalate, suspended in a mixture of 1,2-butanediol and 1,2-decanediol, is exposed to microwave radiation. No new phase
containing both types of the guest molecules was observed when the 1-propanol intercalate, suspended in a mixture of 1-propanol
and 1,2-octanediol, is exposed to microwave radiation. 相似文献
7.
V. Ščasnár L. Beneš Š. Bezek T. Trnovec 《Journal of Radioanalytical and Nuclear Chemistry》1984,82(2):287-297
Simple and rapid extraction method for quantitative and selective isolation of the new local anesthetic pentacaine from biological materials is proposed. The technique of ion-pair formation was found to be more effective than usual access using the extraction of the nonionized species. The extraction yield of the unchanged molecule3H-pentacaine after double extraction and single scrubbing was found to be more than 90%. The radiochemical purity was over 90%. The method appears suitable for pharmacokinetic studies in the animal body. 相似文献
8.
Ludvík Beneš Klára Melánová Vítězslav Zima Jaroslava Kalousová Jiří Votinský 《Journal of inclusion phenomena and macrocyclic chemistry》1998,31(3):275-286
Recent knowledge of the kinetics and intercalation mechanisms are summarized and accompanied by examples of intercalation reactions of water and ethanol into anhydrous vanadyl phosphate and redox intercalation of alkali metal cations into vanadyl phosphate dihydrate. Three possible mechanisms of intercalation are presented which are based on: (i) a concept of exfoliation of layers; (ii) the formation of stages and randomly stacked layers; (iii) co-existence of intercalated and non-intercalated parts of crystals of the host separated by an advancing phase boundary. The corresponding kinetic curves are ascribed to mechanisms (ii) and (iii). 相似文献
9.
Ludvík Beneš Vítězslav Zima 《Journal of inclusion phenomena and macrocyclic chemistry》1994,20(4):381-391
The course of intercalation of water into 1-VOPO4 has been studied by thermomechanical analysis and X-ray diffraction. Neither formation of vanadyl phosphate monohydrate nor staging were observed during the intercalation. The broadening and the shift of the positions of the lines in the diffractograms have been explained by the random stacking of intercalated and nonintercalated layers in the sample. 相似文献
10.