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71.
Lali Chatterjee 《Annalen der Physik》1979,491(2):148-160
The Energy levels of a muonic atom, taking electron screening into account are determined by directly solving the Dirac Equation in a screened Coulomb potential of the ALLIS-MORSE type. The non-relativistic limit of the result agrees with the values obtained by solving the Schrödinger Equation for a muon in such a potential. The deviation from the Coulomb case is of the form 3 exp (?xZm/me), where x ≈ 2 to 7 for the 1S1/2 state and is thus small if values of a1 are taken from the tables of ALLIS and MORSE. However these values, fitted to electron-scattering experiments may not be relevant for muonic atoms so that experimental determination of a1 for muonic atoms is required. If a1 should be smaller, the perturbation of the Coulomb levels would be greater, especially for the outer shells, and one could vary the parameter a1 to a1 to fit the results with experiments. 相似文献
72.
Katina S.S. Dossou Patrice Chiap Bezhan Chankvetadze Anne-Catherine Servais Marianne Fillet Jacques Crommen 《Journal of chromatography. A》2009,1216(44):7450-7455
A polysaccharide-based chiral stationary phase (Sepapak-4), with cellulose tris(4-chloro-3-methylphenylcarbamate) as chiral selector, has been investigated in liquid chromatography (LC). Its enantioresolution power was evaluated towards 13 basic amino-drugs with widely different structures and polarities, using polar organic mobile phases. After preliminary experiments, acetonitrile was selected as the main mobile phase component, to which a low concentration of diethylamine (0.1%) was systematically added in order to obtain efficient and symmetrical peaks. Different organic solvents were first added in small proportions (5–10%) to acetonitrile to modulate analyte retention. Polar organic modifiers were found to decrease retention and enantioresolution while hexane had the opposite effect, indicating normal-phase behaviour under these conditions. The addition of an organic acid (formic, acetic or trifluoroacetic acid) was found to strongly influence the retention of the basic amino drugs in these nonaqueous systems. The nature and proportion of the acidic additive in the mobile phase had also deep impact on enantioresolution. Therefore, the studied compounds could be subdivided in three groups in respect to the acidic additive used. All analytes could be enantioseparated in relatively short analysis times (10–20 min) using these LC conditions. 相似文献
73.
Enantioseparations of chiral compounds were studied in nonaqueous capillary electrochromatography (NAQ CEC) with cellulose and amylose tris(3,5-dimethylphenylcarbamates) (Chiralcel OD and Chiralpak AD, respectively) coated on the silica gels of various pore and particle size. Increasing intraparticle perfusive transport with increasing pore size of silica favorably affected peak efficiency and resolution of enantiomers, although some decrease of separation factor was observed in the pore size range 60-200 A. Further improvement of peak efficiency was observed when the particle size of silica was reduced from 5 to 3 microm. The effects of a separation medium and temperature are also reported and the data obtained in the same capillaries in CEC and capillary liquid chromatography (LC) mode are compared. 相似文献
74.
A. A. Vedenyapin B. G. Chankvetadze E. I. Klabunovskii 《Reaction Kinetics and Catalysis Letters》1984,24(1-2):77-80
Studies of the effect of preparation conditions on the activity and enantioselectivity of asymmetric Cu–Ni catalysts have revealed their great dependence and two maxima in the dependence of the optical yield on the pH of the modifying solution. Cu–Ni catalysts are shown to have similar catalytic properties in a wide range of their Cu content.
, Cu–Ni . pH , Cu–Ni .相似文献
75.
Chankvetadze B Burjanadze N Pintore G Bergenthal D Bergander K Mühlenbrock C Breitkreuz J Blaschke G 《Journal of chromatography. A》2000,875(1-2):471-484
Opposite migration order was observed for the enantiomers of brompheniramine [N-[3-(4-bromphenyl)-3-(2-pyridyl)propyl]-N,N-dimethylamine] (BrPh) in capillary electrophoresis (CE) when native beta-cyclodextrin (beta-CD) and heptakis(2,3,6-tri-O-methyl)-beta-CD (TM-beta-CD) were used as chiral selectors. NMR spectrometry was applied in order to obtain information about the stoichiometry, binding constants and structure of the selector-selectand complexes in solution. The data were further confirmed by UV spectrometry and electrospray ionization mass spectrometry. The structure of the complexes in the solid state was determined using X-ray crystallography performed on the co-crystals precipitated from the 1:1 aqueous solution of selector and selectand. This multiple approach allowed an elucidation of the most likely structural reason for a different affinity (binding strength) of BrPh enantiomers towards beta-CD and TM-beta-CD. However, the question about a force responsible for the opposite affinity pattern of BrPh enantiomers towards these CDs could not be answered definitely. 相似文献
76.
The review summarizes recent developments in enantioseparations by capillary electrochromatography (CEC). Selected fundamental aspects of CEC are discussed in order to stress those features which may allow the success of this technique in the competitive field of enantioseparations. In addition, the comparative characteristics of the different modes of chiral CEC and the stationary phases are presented. The effects of the characteristics of the stationary and liquid phases and operational conditions on the separation results are discussed. Finally, some future trends are briefly addressed. 相似文献
77.
Chankvetadze B Burjanadze N Maynard DM Bergander K Bergenthal D Blaschke G 《Electrophoresis》2002,23(17):3027-3034
Twenty-three cationic chiral analytes were resolved in capillary electrophoresis using native beta-cyclodextrin and single isomer heptakis-(2-O-methyl-3,6-di-O-sulfo)-beta-cyclodextrin as chiral selectors. For 12 of 16 chiral analytes resolved with both chiral selectors the enantiomer migration order was opposite. In selected cases the structure of cyclodextrin-analyte complexes in aqueous solution was investigated using one-dimensional transverse rotating frame nuclear Overhauser and exchange spectroscopy. It was found that in contrast to mainly inclusion-type complexes between chiral analytes and beta-cyclodextrin, external complexes are formed between the chiral analytes and structurally crowded, highly charged heptakis-(2-O-methyl-3,6-di-O-sulfo)-beta-cyclodextrin. 相似文献
78.
Paola Peluso Alessandro Dessì Roberto Dallocchio Barbara Sechi Carlo Gatti Bezhan Chankvetadze Victor Mamane Robin Weiss Patrick Pale Emmanuel Aubert Sergio Cossu 《Molecules (Basel, Switzerland)》2021,26(1)
The chalcogen bond (ChB) is a noncovalent interaction based on electrophilic features of regions of electron charge density depletion (σ-holes) located on bound atoms of group VI. The σ-holes of sulfur and heavy chalcogen atoms (Se, Te) (donors) can interact through their positive electrostatic potential (V) with nucleophilic partners such as lone pairs, π-clouds, and anions (acceptors). In the last few years, promising applications of ChBs in catalysis, crystal engineering, molecular biology, and supramolecular chemistry have been reported. Recently, we explored the high-performance liquid chromatography (HPLC) enantioseparation of fluorinated 3-arylthio-4,4′-bipyridines containing sulfur atoms as ChB donors. Following this study, herein we describe the comparative enantioseparation of three 5,5′-dibromo-2,2′-dichloro-3-selanyl-4,4′-bipyridines on polysaccharide-based chiral stationary phases (CSPs) aiming to understand function and potentialities of selenium σ-holes in the enantiodiscrimination process. The impact of the chalcogen substituent on enantioseparation was explored by using sulfur and non-chalcogen derivatives as reference substances for comparison. Our investigation also focused on the function of the perfluorinated aromatic ring as a π-hole donor recognition site. Thermodynamic quantities associated with the enantioseparation were derived from van’t Hoff plots and local electron charge density of specific molecular regions of the interacting partners were inspected in terms of calculated V. On this basis, by correlating theoretical data and experimental results, the participation of ChBs and π-hole bonds in the enantiodiscrimination process was reasonably confirmed. 相似文献
79.
In this overview the goal of the authors was to analyze from the historical perspective the reasons of success and failure of chiral capillary electrophoresis. In addition, the current trends are analyzed, unique advantages of capillary electrophoresis are highlighted and some future directions are discussed. 相似文献
80.
P.S. Remya Devi Shreeram Joshi Rakesh Verma A.M. Lali L.M. Gantayet 《Radiation Physics and Chemistry》2010,79(1):41-45
Effects of gamma radiation on indigenous strong cation and anion exchange resins have been studied in HCl medium up to a dosage of 3600 kGy. The ion exchange capacities of cation and anion exchangers decreased by around 20% at 2400 kGy of absorbed dose. Decrease in salt-splitting capacity and total exchange capacity for both cation and anion exchangers were comparable up to 2400 kGy. Above 2400 kGy, a marginal loss in the capacity was observed for cation exchangers whereas a drastic reduction was noticed for the anion exchangers. The distribution coefficients for zirconium, antimony and cobalt, measured in HCl medium, did not change significantly for 2400 kGy of absorbed dose. Crushing strength and moisture retention capacity did not exhibit any specific trend with the absorbed dose. 相似文献