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101.
GSH and L-His are abundant biomolecules and likely biological ligands for Zn(II) under certain conditions. Potentiometric titrations provide evidence of formation of ternary Zn(II) complexes with GSH and L-His or D-His with slight stereoselectivity in favour of L-His (ca. 1 log unit of stability constant). The solution structure of the ZnH(GSH)(L-His)(H2O) complex at pH 6.8, determined by NMR, includes tridentate L-His, monodentate (sulfur) GSH, and weak interligand interactions. Calculations of competitivity of this complex for Zn(II) binding at pH 7.4 indicate that it is likely to be formed in vivo under conditions of GSH depletion. Otherwise, GSH alone emerges as a likely Zn(II) carrier. 相似文献
102.
103.
We consider natural exponential families of Lévy processes with randomized parameter. Such processes are Markov, and under suitable assumptions, pairs of such processes with shared randomization can be “stitched together” into a single harness. The stitching consists of deterministic reparametrization of the time for both processes, so that they run on adjacent time intervals, and of the choice of the appropriate law at the boundary. 相似文献
104.
Jacek Polewczak 《Journal of statistical physics》2000,100(1-2):327-362
Existence of global-in-time, spatially inhomogeneous, and L
1-renormalized solutions is proven for the model of simple reacting spheres under the assumptions that initially the system has a finite total mass, energy, and entropy. 相似文献
105.
Jacek Lubczak 《国际化学动力学杂志》2010,42(9):550-561
To establish the mechanism of reaction of formation of oligoetherols with perhydro‐1,3,5‐triazine ring, the kinetics of reaction of isocyanuric acid and 1,3,5‐tris(2‐hydroxyetyl) isocyanurate with ethylene carbonate resulting in formation of polyetherols in the presence of diazabicyclo[2.2.2]octane as a catalyst has been investigated. The kinetic and mechanistic studies revealed that the initial step of reaction is zero order related to ethylene carbonate and the reaction is inhibited by imide groups of isocyanuric acid. The mechanism of reaction was confirmed by spectroscopic and electrochemical methods. © 2010 Wiley Periodicals, Inc. Int J Chem Kinet 42: 550–561, 2010 相似文献
106.
Krystyna Wejroch Jerzy Lange Anna Kielak Janina Karolak‐Wojciechowska Jacek Sonicki Tadeusz Jagodziski 《Journal of heterocyclic chemistry》2001,38(4):877-884
Bis(ethoxycarbonyl)alkylidene derivatives 4 and 5 of the respective title hydrazones were obtained in the reactions with diethyl oxomalonate, diethyl oxosuccinate, diethyl 2‐oxoglutarate, and diethyl oxalo‐propionate as mixtures of geometric isomers with high predominance of one of them. On heating at 160‐200° without any solvent or on refluxing in ethanol 4 cyclized to yield the corresponding pyri‐dazino[6, 1‐c]triazines 6 , whereas heating of 5 gave, depending on the chain length, the corresponding pyra‐zolylpyridazines 8b and 8d or the pyridazinylpyridazine 8c . X‐ray analysis was used to determine the structures of 6 and 8 ; the unit cell of 6c was found to accommodate 16 molecules representing four conforma‐tional varieties. The different behavior of 4 and 5 in the cyclization reactions was interpreted in terms of the tautomeric equilibrium which was shifted towards the enamine form in 4 , and towards the imine form, in 5 . Transmission of a long‐range chirality effect in 4d and 5a‐d manifested itself in the 1H nmr spectra as the magnetic non‐equivalence of the CH2 protons in one or both ester ethyl groups. 相似文献
107.
Jacek Achrem‐Achremowicz Elżbieta Kępczyńska Marek Żylewski Zbigniew Janeczko 《Biomedical chromatography : BMC》2010,24(3):261-267
A series of superlipophilic or highly lipophilic semisynthetic betulin derivatives was prepared and their relative lipophilicity was measured by reversed‐phase thin‐layer chromatography (RP‐TLC) at different pH values using 1,4‐dioxane–acetate buffer mixtures as mobile phases. Cholesterol, 17β‐estradiol and pure betulin were used as the reference compounds. Linear relationships were found between RM values and 1,4‐dioxane concentrations in the mobile phases. LogP values were also calculated with computer programs ACD/LogP (ChemSketch 11.0, Advanced Chemistry Development Inc.) and ClogP (Daylight Chemical Information Systems Inc.). The empirical and theoretical data were compared, and the RM0 values correlated well with logP. Two of the synthesized betulin derivatives are reported for the first time. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
108.
Organofunctional silanes with more sterically hindered substituents at the silicon atom than the typical methoxy (ethoxy) group have lately been frequently used as silane coupling agents, in polymer coupling systems, sol‐gel processes and also as interpenetrating polymer network substrates. New and very efficient synthetic ways leading to organofunctional silanes of the above type with methacryl, amine, chloro and isocyanato functional groups are proposed here. Catalytic transesterification and/or alcoholysis of chloropropyltrialkoxysilanes followed bynucleophilic substitution has been employed. Copyright © 2001 John Wiley & Sons, Ltd. 相似文献
109.
Jacek Sochacki 《Fiber and Integrated Optics》1989,8(2):107-119
The most recent formulation of the perfect geodesic lens problem is utilized to evaluate a novel solution. This solution describes a smooth geodesic depression profile with a finite value of its local curvature radius at the edge of the lens. This feature should minimize radiation and scattering losses by the guided modes that take place mainly at the lens boundary. The external rounded section of the proposed lens is described by a simple, explicit expression that considerably eases designing procedure. The presented lens is capable of perfect focusing once the theoretically prescribed ideal depression profile is accurately fabricated. For straightforward examination of the influence of technological grinding errors on the lens focal characteristics, a simple analytical method is proposed and investigated. 相似文献
110.
The areas of zero electrostatic potential within an array of electric charges in an ionic crystal can be represented as a zero equipotential surface (ZEPS), which separates space into domains of positive and negative potential. ZEPS are conventionally expressed in terms of nodal surfaces. We express the coordinates and charge distribution of several ZEPS in terms of the Jacobi theta functions, and provide their graphical visualisation. 相似文献