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31.
Summary The kinetics of anation of chromium(III) species, [Cr(H2O)6]4+ and [Cr(H2O)5OH]2+, by L-phenylalanine in aqueous acid has been studied spectrophotometrically. Effects of varying [substrate], [ligand], [H+], , % ethanol and temperature were investigated. The kinetic data suggest a mechanism where outersphere-associations [between chromium(III) species and phenylalanine in the zwitterionic form] precede anation. Comparison of the results with published data suggest an Ia path for the [Cr(H2O)6]3+ reaction and Id path for the [Cr(H2O)5OH]2+ reaction. 相似文献
32.
Ultrasonic slurry sampling electrothermal atomic absorption spectrometry with a metal tube atomizer has been applied to the determination of lead in Bangladeshi fish samples. The slurry sampling conditions, such as slurry stabilizing agent, slurry concentration, pyrolysis temperature for the slurried fish samples, particle size and ultrasonic agitation time, were optimized for electrothermal atomic absorption spectrometry with the Mo tube atomizer. Thiourea was used as the chemical modifier for the interference of matrix elements. The detection limit was 53 fg (3S/N). The determined amount of lead in Bangladeshi fish samples was consistent with those measured in the dissolved acid-digested samples. The advantages of the proposed methods are easy calibration, simplicity, low cost and rapid analysis. 相似文献
33.
Manzoori JL Amjadi M 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2003,59(5):909-916
The characteristics of host-guest complexation between beta-cyclodextrin (beta-CD) and two forms of ibuprofen (protonated and deprotonated) were investigated by fluorescence spectrometry. 1:1 stoichiometries for both complexes were established and their association constants at different temperatures were calculated by applying a non-linear regression method to the change in the fluorescence of ibuprofen that brought about by the presence of beta-CD. The thermodynamic parameters (deltaH, deltaS and deltaG) associated with the inclusion process were also determined. Based on the obtained results, a sensitive spectrofluorimetric method for the determination of ibuprofen was developed with a linear range of 0.1-2 microg ml(-1) and a detection limit of 0.03 microg ml(-1). The method was applied satisfactorily to the determination of ibuprofen in pharmaceutical preparations. 相似文献
34.
Mohammad R. Ahmady Roberto R. Mendel 《Zeitschrift fur Physik C Particles and Fields》1995,65(2):263-265
The decay rates for the exclusiveB decaysBK
c
andBK*
c
are calculated in the context of the heavy quark effective theory. We obtain(BK
c
)/ (BK)=1.6±0.2 and(BK*
c
)/ (K*)=0.39±0.04. These results lead to estimates BR(BK
c
)=(0.11±0.02)% and BR(BK*
c
)=(0.05±0.01)% if we use the central current experimental values forB(K, K
*) branching ratios. 相似文献
35.
Behforouz M Haddad J Cai W Arnold MB Mohammadi F Sousa AC Horn MA 《The Journal of organic chemistry》1996,61(19):6552-6555
The novel 7-(N-formyl-, 7-(N-acetyl-, and 7-(N-isobutyrylamino)-2-methylquinoline-5,8-diones were synthesized in excellent overall yields in three steps via the nitration of the commercially available 8-hydroxy-2-methylquinoline followed by a reduction-acylation step and then oxidation. Acid hydrolysis of 7-(N-acetylamino)-2-methylquinoline-5,8-dione (14a) afforded the novel 7-aminoquinoline-5,8-dione 7 in excellent yields. Due to our efficient preparation of dione 14a, we now report a short and practical method for the total synthesis of the potent antitumor agent lavendamycin methyl ester (1b) with an excellent overall yield. 相似文献
36.
Nitro aromatic compound can be obtained in high yields via nitration of aromatic compound with wet carbon-based solid acid and NaNO_3 under solvent free oxidation at room temperature. 相似文献
37.
Mohammad Shaharuzzaman James ChickosCheok N. Tam Timothy A. Keiderling 《Tetrahedron: Asymmetry》1995,6(12):2929-2932
The synthesis of (2R,3R) and (2S,3S) dideuteriosuccinic acid in 63 ± 10% enantiomeric excess by reduction of the half acid ester of ethyl fumarate from (R) and (S) BINAP ruthenium (II) diacetate complex, respectively, is reported. (2R,3R) and (2S,3S)-Dideuteriosuccinic acid has also been prepared from (R)-BINAP ruthenium (II) dicarboxylate complex directly in similar optical purity by reversing the sequence of introduction of the isotopic label. 相似文献
38.
David G. Whitten Mohammad S. Farahat Elizabeth R. Gaillard 《Photochemistry and photobiology》1997,65(1):23-32
Abstract— Characterization of short-lived intermediates in homogeneous and microheterogeneous systems has been carried out using time-resolved spectroscopic techniques. The data obtained from these techniques have been analyzed in a relatively unconventional manner to elucidate complex transient behavior for two reactive systems. The highly nonexponential fluorescence decay for a series of fraws-stilbene-derivatized amphiphiles that readily form bilayer systems in aqueous media has been analyzed using a distribution of lifetimes analysis (DLA). The utility of DLA for quantitative studies was first determined by simulation of artificial decay data. Despite some limitations in DLA, qualitative conclusions as to the nature of the fluorescing species may be drawn when supplementary information such as steady-state spectroscopic data are also considered. The results indicate that the observed fluorescence originates from different types of excited-state species that consist of two or more trans-stilbene units; one of the emissions is attributed to the excited state of a ground-state aggregate while the other is assigned to an excimer that may arise from a 'defect'in the bilayer. The nonexponential nature of the decays is attributed to distributions of environments experienced by the fluorescing species. Electron transfer (ET) reactions between several excited pinacols and carbon tetrachloride in solution have been found to yield products with quantum yields that are higher than unity in the presence of oxygen, suggesting a chain mechanism for product formation. In these systems both the donor and the acceptor undergo bond fragmentation following the initial ET step. The individual steps involved in the proposed mechanism for these systems have been investigated in part using different steady-state and time-resolved laser spectroscopic techniques. However, it was also necessary to utilize pulse radiolysis in order to confirm the involvement of certain radical intermediates that were not observable by the usual flash photolysis techniques. 相似文献
39.
Mohammad Malakootian Hakimeh Mahdizadeh Abbas Dehdarirad 《Journal of Dispersion Science and Technology》2019,40(6):846-854
Ciprofloxacin is used in the treatment of bacterial infections. Because ciprofloxacin is not effectively degraded by biological processes, advanced oxidation processes such as photocatalytic ozonation are applied to remove this antibiotic from wastewater. The aim of this study was to investigate photocatalytic ozonation for the removal of ciprofloxacin from aquatic environments and optimization of the effective parameters of the process. For this purpose, ZnO nanoparticles were synthesized using the thermal method and immobilized on the surface of stones. The structural properties of the nanoparticles were determined by XRD, TEM, Photoluminescence (PL) and SEM. Experiments were carried out in a Plexiglas reactor supported with the continuous injection of ozone. The effective parameters for removal efficiency were reaction time, initial concentration of ciprofloxacin, pH, photocatalyst concentration and reaction kinetics. The highest ciprofloxacin removal efficiency occurred at the following optimal conditions: pH of 7, reaction time of 30?min, photocatalyst concentration of 3?g/L and initial ciprofloxacin concentration of 10?mg/L. Removal efficiency of 96% was obtained under these conditions. Linear kinetic models showed that the process followed pseudo-first order and Langmuir-Hinshelwood kinetics. This process had a high removal efficiency and suitable for removal of ciprofloxacin from aquatic environments.GRAPHICAL ABSTRACT 相似文献
40.
Dynamic headspace liquid-phase microextraction of alcohols 总被引:3,自引:0,他引:3
Saraji M 《Journal of chromatography. A》2005,1062(1):15-21
A method was developed using dynamic headspace liquid-phase microextraction and gas chromatography-mass spectrometry for extraction and determination of 9 alcohols from water samples. Four different solvents, hexyl acetate, n-octanol, o-xylene and n-decane were studied as extractants. The analytes were extracted using 0.8 microl of n-octanol from the headspace of a 2 ml sample solution. The effect of sampling volume, solvent volume, sample temperature, syringe plunger withdrawal rate and ionic strength of the solution on the extraction performance were studied. A semiautomated system including a variable speed stirring motor was used to ensure a uniform movement of syringe plunger through the barrel. The method provided a fairly good precision for all compounds (5.5-9.3%), except methanol (16.4%). Detection limits were found to be between 1 and 97 microg/l within an extraction time of approximately 9.5 min under GC-MS in full scan mode. 相似文献