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排序方式: 共有450条查询结果,搜索用时 31 毫秒
1.
Goudarzy Forough Zolgharnein Javad Alizadeh Vahid 《Journal of Analytical Chemistry》2022,77(6):711-716
Journal of Analytical Chemistry - In this article, a new spectrofluorometric method was developed for the determination of methamphetamine based on a turn-on luminescence response of captopril... 相似文献
2.
A sensitive and efficient method for trace analysis of some phenolic compounds using simultaneous derivatization and air‐assisted liquid–liquid microextraction from human urine and plasma samples followed by gas chromatography–nitrogen phosphorous detection 下载免费PDF全文
Mir Ali Farajzadeh Mohammad Reza Afshar Mogaddam Ali Akbar Alizadeh Nabil 《Biomedical chromatography : BMC》2015,29(12):1921-1931
In present study, a simultaneous derivatization and air‐assisted liquid–liquid microextraction method combined with gas chromatography–nitrogen phosphorous detection has been developed for the determination of some phenolic compounds in biological samples. The analytes are derivatized and extracted simultaneously by a fast reaction with 1‐flouro‐2,4‐dinitrobenzene under mild conditions. Under optimal conditions low limits of detection in the range of 0.05–0.34 ng mL?1 are achievable. The obtained extraction recoveries are between 84 and 97% and the relative standard deviations are less than 7.2% for intraday (n = 6) and interday (n = 4) precisions. The proposed method was demonstrated to be a simple and efficient method for the analysis of phenols in biological samples. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
3.
4.
Mohammad H. Alizadeh Toktam Kermani Reza Tayebee 《Monatshefte für Chemie / Chemical Monthly》2007,138(2):165-170
Summary. Esterifications of acetic acid with some linear, secondary, tertiary, and benzylic alcohols mediated by catalytic amounts
of Keggin, Wells–Dawson, and Preyssler type heteropolyacids were carried out under reflux at mild reaction conditions with good to excellent yields. Among the examined
catalysts, H3PW12O40 and H14NaP5W30O110 revealed better results than other heteropolyacids. This work was performed with the aim of simplifying the esterification
process by omitting any solvents and mineral acid catalysts. Easy work-up, low cost, and acidic waste reduction, which are
all important features from the environmental and economical points of view, are distinct aspects of this protocol. Heteropolyacid
catalysts could be separated after a simple work-up and reused for several times. 相似文献
5.
Summary. A highly efficient, selective, fast, and cheap protocol is developed for oxidation of aromatic amines and alcohols utilizing
34% hydrogen peroxide in water catalyzed by some W- and Mo-based heteropolyoxometalates. Findings showed that dodecatungstophosphoric
acid, H3PW12O40, was the most efficient catalyst in the examined oxidation reactions. This methodology may prove to be a valuable alternative
for eco-friendly green oxidation. Inherent simplicity, easy work up, and using regenerable catalysts were other key aspects
of this oxidation protocol. 相似文献
6.
Hindered internal rotation about the C‐N single bonds joining the thiuram disulfide was studied by 1H NMR complete line‐shaped analysis in different dimethyl sulfoxide‐chloroform (DMSO‐CDCl3) mixtures. From the temperature dependence of methyls proton spectra, activation parameters (Ea, ΔH≠, ΔS≠, and ΔG≠) were obtained. The Arrhenius plots showed a distinct isokinetic temperature at about 35 °C at which the exchange rate is more or less independent of the solvent composition. The resulting ΔH≠ against TΔS≠ plot showed a firmly good linear correlation, indicating the existence of an enthalpy‐entropy composition in an exchange process. 相似文献
7.
An effective route to novel maleimides is described, which involves the reaction of an enamine derived from the addition of a secondary amine to a dialkyl acetylenedicarboxylate with an arylsulfonyl isocyanate. These maleimides in solution indicate dynamic NMR because of restricted rotation around the carbon-nitrogen bond, resulting from conjugation of the side-chain nitrogen with the adjacent α,β-unsaturated ester group. 相似文献
8.
Proton NMR was used to study the complexation reaction between silver ion and hexathia-18-crown-6 in a number of binary mixed solvents of dimethyl sulfoxide with acetonitrile and methanol. Formation constants for the resulting 1:1 complexes in different solvent mixtures were determined by computer fitting of the chemical shift-mole ratio data. The influence of solvent composition on the stability of the resulting complex is discussed. The exchange kinetics of Ag+-hexathia-18-crown-6 in 70-30 wt.% dimethyl sulfoxide-acetonitrile and 75-25 wt.% dimethyl sulfoxide-methanol were studied by proton NMR line-shape analysis. In both solvent mixtures, the exchange of thiacrown ether between the free and complexed sites was found to proceed via a dissociative pathway. The exchange rates and the activation parameters E
a, H
, S, and G for the ligand exchange were determined and the influence of solvent properties on these parameters discussed. 相似文献
9.
Abolghasem Moghimi Robabeh Alizadeh Hossein Aghabozorg Abbas Shockravi M. Carla Aragoni Francesco Demartin Francesco Isaia Vito Lippolis Andrew Harrison A. Shokrollahi Mojtaba Shamsipur 《Journal of Molecular Structure》2005,750(1-3):166-173
The one-pot reaction between the novel proton transfer compound (pydaH2)2+(phendc)2−, LH2, and Cu(II) afforded the compounds (pydaH)2[Cu(phendc)2]·10H2O, 1, and (pydaH)2[Cu(phendc)(phendcH)]2·5H2O, 2, where pyda=2,6-diaminopyridine, and phendcH2=1,10-phenanthroline-2,9-dicarboxylic acid. The single crystal X-ray diffraction analysis of 1 and 2 revealed that these are two novel self-assembled 3D Cu(II) complex-organo-networks, in which (pydaH)+ ions and [Cu(phendc)2]2− or complex units are held together by ion pairing, H-bonding, and π–π interactions. Magnetic measurements over the temperature range 1.8–310 K revealed no significant magnetic coupling between Cu(II) centers in 1 or 2. 相似文献
10.
Mojtaba Shamsipur Tahereh Poursaberi Morteza Hosseini Naader Alizadeh Mohammad Reza Ganjali 《Analytica chimica acta》2004,501(1):55-60
A highly sensitive and selective fluorimetric optode membrane for the determination of ultra trace amounts of Ni2+ ions was prepared. The plasticized PVC-membrane incorporating potassium tetrakis(p-chlorophenyl)borate (KTpClPB) and 2,5-thiophenylbis(5-tert-butyl-1,3-benzexazole) (TTBB), as a highly fluorescent chromoionophore, displays a calibration response for Ni2+ ions over a wide concentration range of 1.0×10−3 to 1.0×10−8 M. It has a relatively fast response of <40 s. In addition to high stability and reproducibility, and relatively long working lifetime, the sensor possesses good selectivity for nickel ions over several common diverse ions. The fluorescence signal of the optode membrane can be easily recovered by immersion in EDTA solution. The optode was applied successfully to the determination of traces of Ni2+ ion in edible oil and a wastewater sample from nickel electroplating industries. 相似文献