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31.
A flow-injection method is reported for the determination of thyroxine based on its enhancement effect on the tris(2,2'-bipyridyl)ruthenium(III) chemiluminescence reaction in the presence of NADH using immobilized alcohol dehydrogenase purified from baker yeast. The limit of detection (3 sigma blank) was 5.0 x 10(-8) M with a sample throughput of 80 h(-1). The calibration graph was linear over the range 0.5 - 10 x 10(-7) M (r2= 0.9988) with the relative standard deviation in the range 1.4 - 3.5% (n = 4). The effect of common excipients used in pharmaceutical preparations, some organic compounds and metal ions was studied. The method was applied to pharmaceutical thyroxine tablets, and the obtained results were not significantly different from the amount quoted. 相似文献
32.
Parviz Norouzi Gholam-Reza Nabi Bidhendi Mohammad Reza Ganjali Ali Sepehri Maryam Ghorbani 《Mikrochimica acta》2005,149(1-2):123-129
A novel chemiluminogenic reagent, refered to as spiro form fluorescein hydrazide, was synthesized, and its application to chemiluminescence (CL) determination of Co2+ is described. The method is based on the catalytic effect of Co2+ on the autoxidation of sulfite in basic solution to generate a series of powerful oxidative intermediates, which then oxidize colorless, nonfluoresent fluorescein hydrazide to generate strong CL emission. The CL signal is linearly related to the concentration of Co2+ in the range of 0.1–200nM with a detection limit of 0.04nM. The optimal conditions for the detection of Co2+ were evaluated, and the possible CL mechanism is discussed. The proposed method has been applied to the determination of Co2+ in pharmaceutical preparations and in soil samples. 相似文献
33.
Mohsin Qureshi Syed Ashfaq Nabi Ali Mohammad Pushkin Mohammad Qureshi 《Journal of solid state chemistry》1982,44(2):186-191
The kinetics and mechanism of the reaction of 2,4-dinitrotoluene with diphenylamine were studied in the solid state. The reaction product is a charge transfer complex with a localized intermolecular interaction as shown by uv and ir spectroscopy. The solid-state studies were complemented by some NMR studies in CCl4. A novel feature of the study reveals that diphenylamine in this case is a much more powerful n donor than a π donor. 相似文献
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Stannic selenites have been synthesized under a variety of conditions. The most stable sample is prepared by mixing 0-0.5M solutions of stannic chloride and sodium selenite in the ratio of 1:1 at pH 1. It is a bifunctional amorphous material. A tentative structure has been proposed on the basis of chemical composition, pH titrations, infrared and thermogravimetric analyses. Its ion-exchange capacity is 0.75 and 0.73 meq g after drying at 50 degrees and 500 degrees respectively. Its analytical importance has been established by the following quantitative separations: Cu(2+) from Ni(2+), Co(2+), Fe(3+), Ga(3+) and In(3+), Fe(3+) from Pb(2+) and Sc(3+), and Sc(3+) from VO(2+). 相似文献
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This Communication describes a cascade reaction sequence that leads to highly functionalized cyclohexenones starting from reaction of cyclobutenones with alpha-lithio-alpha,beta-unsaturated sulfones and amides. The hexatriene-cyclohexadiene cyclization steps presumed to be involved in these transformations are among the most facile hexatriene electrocyclizations reported thus far. 相似文献
38.
A flow-injection method for the determination of serine using a mini-column containing immobilized serine dehydratase isolated and purified from rat liver is described. Ammonia produced from the enzymatic reaction is coupled with hypochlorite and phenol in an alkaline medium yields a blue product due to the indophenol anion formation, which is the basis of a spectrophotometric detection at 640 nm. The limit of detection (2×blank noise) is 0.01 mM with a sample throughput of 25 h−1. Calibration graph is linear in the range 0.2–1.0 mM, with relative standard deviation 0.6–1.0%. 相似文献
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Attiq-Ur-Rehman Mohammad Yaqoob Abdul Nabi 《International journal of environmental analytical chemistry》2013,93(9):603-612
A simple and rapid flow injection (FI) method is reported for the determination of arsenic(V) based on luminol chemiluminescence (CL) detection. The molybdoarsenic heteropoly acid formed by arsenic and ammonium molybdate in the presence of ammonium vanadate in acidic conditions generated chemiluminescence emission via the oxidation of luminol. The limit of detection was 0.15 μg L?1, with a sample throughput 120 h?1. A linear calibration graph was obtained over the range 0.15 to 7.5 μg L?1 (r 2 = 0.9989; n = 9) with relative standard deviation (n = 4) in the range 0.8 to 2.5%. Interfering cations were removed by passing the sample through an in-line iminodiacetate chelating column and phosphate (at 0.6 mg L?1) was removed off-line by magnesium-induced coprecipitation (MAGIC) method. The method was applied to freshwater samples and the results obtained were in reasonable agreement with the results obtained using HGAAS as the reference method. 相似文献