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排序方式: 共有333条查询结果,搜索用时 15 毫秒
1.
I. H. Qureshi M. S. Chaudhary S. Ahmad 《Journal of Radioanalytical and Nuclear Chemistry》1982,68(1-2):209-218
Instrumental neutron activation analysis technique has been used to determine the concentration levels of 12 trace elements
in human head hair samples collected from 105 individuals living in various areas of Rawalpindi-Islamabad. The data show that
the average concentrations of Mn, Co, Ag and Au are higher in the female group as compared to the male group. Four individuals
were found to have elevated levels of Se due to the use of anti-dandruff shampoos, whereas two individials had elevated levels
of Hg. 相似文献
2.
M. S. Chaudhary S. Ahmad A. Mannan I. H. Qureshi 《Journal of Radioanalytical and Nuclear Chemistry》1984,83(2):387-396
An instrumental neutron activation analytical (INAA) technique is described for the determination of 26 toxic and other trace elements in Eastern Coal (NBS SRM-1632a), local coal and its ash. The coal ash was produced by heating coal at 750°C in a muffled furnace. The transfer of these elements to the environment on the complete compustion of coal is estimated from the difference between the elemental concentration of coal and its ash. 相似文献
3.
Samuel K Yin W Stearns RA Tang YS Chaudhary AG Jewell JP Lanza T Lin LS Hagmann WK Evans DC Kumar S 《Journal of mass spectrometry : JMS》2003,38(2):211-221
Metabolic activation of drug candidates to electrophilic reactive metabolites that can covalently modify cellular macromolecules may result in acute and/or idiosyncratic immune system-mediated toxicities in humans. This presents a significant potential liability for the future development of these compounds as safe therapeutic agents. We present here an example of an approach where sites of metabolic activation within a new drug candidate series were rapidly identified using online liquid chromatography/multi-stage mass spectrometry on an ion trap mass spectrometer. This was accomplished by trapping the reactive intermediates formed upon incubation of compounds with rat and human liver microsomes as their corresponding glutathione conjugates and mass spectral characterization of these thiol adducts. Based on the structures of the GSH adducts identified, potential sites and mechanisms of bioactivation within the chemical structure were proposed. These metabolism studies were interfaced with iterative structural modifications of the chemical series in order to block these bioactivation sites within the molecule. This strategy led to a significant reduction in the propensity of the compounds to undergo metabolic activation as evidenced by reductions in the irreversible binding of radioactivity to liver microsomal material upon incubation of tritium-labeled compounds with this in vitro system. With the efficiency and throughput achievable with such an approach, it appears feasible to identify and address the metabolic activation potential of new drug leads during routine metabolite identification studies in an early drug discovery setting. 相似文献
4.
2‐Acetyl thiophenethiocynate (ATT) was synthesized and its characterization study was carried out using elemental analysis, IR and NMR techniques. The new reagent was proposed as an extractant for the development of the extractive spectrophotometric method for determination of Pt(IV) metal. The reagent complexes with the metal to produce a yellow colored complex which was then extracted into ethyl acetate at pH 11.2–11.6 having an absorption maxima at 400 nm. The thermal study showed that the extraction reactions are exothermic in nature with the reagent, and the stoichiometric ratio of Pt(IV) to 2‐acetyl thiophenethiocynate in the organic phase was 1:2. The method permits separation and determination of platinum from real and binary mixtures. The separation of Pt(IV) from bivalent metal ions has been also studied. 相似文献
5.
S. Ahmad M. S. Chaudhary A. Mannan I. H. Qureshi 《Journal of Radioanalytical and Nuclear Chemistry》1983,78(2):375-383
The concentration of certain toxic and essential elements in various brands of tea consumed locally were determined using instrumental neutron activation analysis. Transference of these elements into the drinkable portion was studied by brewing and boiling tea leaves for two minutes and the approximate intake was calculated from this data. The toxic effects of Hg, Se, As, Br and Sb are briefly discussed. 相似文献
6.
Sorption of europium on zirconium oxide has been studies as a function of shaking time, concentration and nature of electrolyte. The effect of initial europium concentration and the amount of adsorbent has been investigated in the range from 6.6·10–10 to 6.6·10–8 mol·dm–3 and between 10 to 200 mg of the oxide. Maximum sorption (>99.8%) from pH 10 buffer and low sorption (<3%) was observed from 0.01 mol·dm–3 nitric or perchloric acid solution. Citrate, sulfate, EDTA and carbonate reduced the sorption significantly. Under optimal conditions Ag(I), Cs(I), Tc(VII), Sb(V), Cu(II), Nd(III), Fe(III), and especially Nd and Fe showed low distribution coefficients. The data followed both Dubinin-Radushkevich and Langmuir-type isotherms. The mean free energy, of sorption was evaluated to be 10.1 kJ mol–1 and the sorption capacity was found to be 22.2 mmol g–1, using the Dubinin-Radushkevich isotherm. 相似文献
7.
Ramesh C. Kapoor Raj N. Mehrotra Shared K. Vajpai Purnima Chaudhary 《Transition Metal Chemistry》1991,16(1):65-70
Summary The kinetics of the OsVIII-catalysed oxidation of glycols by alkaline hexacyanoferrate(III) ion exhibits zerothorder dependence in [Fe(CN)
6
3–
] and first-order dependence in [OsO4]. The order with respect to glycols is less than unity, whereas the rate dependence on [OH–] is a combination of two rate constants; one independent of and the other first-order in [OH–]. These observations are commensurate with a mechanism in which two complexes, [OsO4(H2O)G]– and [OsO4(OH)G]2–, are formed either from [OsO4(H2O)(OH)]– or [OsO4(OH)2]2– and the glycol GH, or by [OsO4(H2O)2] and [OsO4(H2O)(OH)]– and the glycolate ion, G–, which is in equilibrium with the glycol GH through the reaction between GH and OH–. Hence there is an ambiguity about the true path for the formation of the two OsVIII-glycol complexes. A reversal in the reactivity order of glycols in the two rate-determining steps, despite the common attack of OH– ion on the two species of OsVIII-complexes, indicates that the two complexes are structurally different because S changes from the negative (corresponding to k11) to positive (related to k2). 相似文献
8.
Sachin B. Pandya Urmila H. Patel Kaushik P. Chaudhary Bhavesh N. Socha Nikita J. Patel Bhupesh S. Bhatt 《应用有机金属化学》2019,33(12)
Novel cobalt complex of 4‐amino‐N‐(6‐chloropyridazin‐3‐yl)benzene sulfonamide (sulfachloropyridazine) has been synthesized and characterized by elemental analysis, FT‐IR spectroscopy and magnetic susceptibility (VSM). Cobalt complex of Sulfachloropyridazine (Co‐SCP) crystallized in monoclinic space group P21/n with Z = 4. The structure is solved by direct method and refined to R = 0.099 for 4720 reflections with I ?4σ(I). The results of FT‐IR spectra suggest the binding of cobalt atom to the sulfonamide ligand which is in agreement with the crystal structure determination. In crystal structure, molecule is linked via, C‐H … π, C‐Cl … π and π … π intermolecular interactions. The computational studies like the optimization energy and root means square deviation compare with single crystal structure, frontier molecular orbital (Homo‐Lumo energy) and binding energy of the Co‐SCP has been carried out using DFT/B3LYP level of theory in gaseous phase. Hirshfeld surfaces and the 2D‐fingerprint analysis are performed to study the nature of interactions and their measurable contributions towards crystal packing. The interaction of the complex with DNA is investigated using viscosity measurement and absorption titration studies. The result shows the complex bind to DNA with intercalative mode with high DNA‐binding constant (Kb). Also, in vivo and in vitro cytotoxic studies are performed using S. pombe cells and brine shrimp lethality bioassay. DNA‐cleavage study shows better cleaving ability of the complex. 相似文献
9.
Ashu Chaudhary R. V. Singh 《Phosphorus, sulfur, and silicon and the related elements》2013,188(3):615-626
Fourteen- to eighteen-membered tetraamide macrocyclic ligands N 4 L 1 -N 4 L 4 have been prepared by the condensation of 1,2-diaminoethane or 1,3-diaminopropane with malonic or succinic acid in the presence of condensing reagents dicyclohexylcarbodiimide and 4-dimethylaminopyridine. On reduction, these macrocyclic ligands give a new series of tetraazamacrocycles MacL 1 -MacL 4 which form complexes with tin(II) chloride. The ligands and their complexes were characterized by elemental analyses, molecular weight determinations, infrared and 1 H NMR spectral studies. The hexacoordinated state for tin has been confirmed by spectral studies. An octahedral geometry for these complexes has been proposed as the binding sites are the nitrogen atoms of the macrocycles. On the basis of the chemical composition the representation of the complexes as [Sn(MacL n )Cl 2 ] (n = 1-4) has been established. The ligands and their complexes also have been screened for their antifungal and antibacterial activities and the findings have been reported and explained. 相似文献
10.
Aarti Gupta Pragati Devi Priyanka Chaudhary Dharma Kishore 《Phosphorus, sulfur, and silicon and the related elements》2013,188(7):808-821
Abstract The synthetic potential of 2,3,4,5-tetrahydrobenzo[b] [1,5]thiazepine-1,1,4-trione-2-carbohydrazide (5) which resulted from ethyl-4-oxo-2,3,4,5-tetrahydrobenzo[b] [1,5]thiazepine-2-carboxylate (3), on its oxidation with H2O2/AcOH followed by treatment with NH2NH2.H2O, was exploited to provide an access to 2-triazolo, 2-oxadiazolo, and 2-pyrazolo substituted derivatives of 1,5-benzothiazepin-4-oxo-1,1-dioxides (6–10), respectively. 相似文献