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151.
Solvent-free reactions were used for the synthesis of a series of imidazolium-based ionic salts: 3,3′-[pyridine-2,6-diylbis(methylene)]bis(1-R-1H-imidazol-3-ium)chloride; (R = methyl, ethyl, butyl, isobutyl, hexyl, and benzyl). A simple and effective filtration process was used to isolate all the products in high purity and with yields ?93% within a 24 h period. The highly pure ionic compounds which are precursors to N-heterocyclic carbene ligands used in catalysis were fully characterized as gray-white hygroscopic salts. 相似文献
152.
Ullah Irfan Baloch Musa Kaleem Ullah Imran Mustaqeem Muhammad 《Journal of solution chemistry》2014,43(8):1360-1373
Journal of Solution Chemistry - The development of a meaningful dissolution procedure for drug products with limited water solubility has been a challenge to both the pharmaceutical industry and... 相似文献
153.
K.K. Abdul Khader Ayyiliath M. Sajith M. Syed Ali Padusha H.P. Nagaswarupa A. Muralidharan 《Tetrahedron letters》2014
In this Letter we report a rapid and facile access to C2-substituted imidazo[4,5-b]pyridine analogues utilizing palladium mediated Buchwald–Hartwig cross-coupling reactions. The use of enolizable heterocycles as cross-coupling partners resulted in a wide range of imidazo[4,5-b]pyridine analogues which are prone to have medicinal relevance. Xantphos and Pd(OAc)2 were found to be more effective for the coupling of 2-halo imidazo[4,5-b]pyridines with pyridone nucleophiles. A regioselective approach for the synthesis of 2-substituted 3H-imidazo[4,5-b]pyridine and 1H-imidazo[4,5-b]pyridine is also reported. 相似文献
154.
155.
Haladhara Naik Ashok Goswami Guinyun Kim Kwangsoo Kim Sung-Chul Yang Muhammad Sahid Muhammad Zaman Manwoo Lee Sung-Gyun Shin Moo-Hyun Cho 《Journal of Radioanalytical and Nuclear Chemistry》2014,299(3):1335-1343
The independent isomeric-yield ratios of 89m,gNb for the 93Nb(γ, 4n) 89m,gNb reaction with bremsstrahlung energies of 45-, 50-, 55-, 60-, and 70-MeV were measured by the activation and the off-line γ-ray spectrometric technique at 100 MeV electron linac of the Pohang accelerator laboratory. The isomeric-yield ratios of 89m,gNb for the natZr(p, xn) 89m,gNb and the 89Y(α, 4n) 89m,gNb reactions were measured by using a stacked-foil activation technique with the proton energies of 19–45 MeV and alpha energies of 38.9-, 40.5-, and 42.5-MeV at the MC-50 cyclotron of Korea Institute of Radiological and Medical Sciences. The measured isomeric-yield ratio of 89m,gNb from the 93Nb(γ, 4n), natZr(p, xn), and 89Y(α, 4n) reactions were compared with the similar literature data in the 89Y(3He, 3n) reaction. It was found that the isomeric yield ratio of 89m,gNb increases with projectile energy, which indicate the effect of excitation energy. However, for the similar compound nucleus with the same excitation energy, the isomeric-yield ratios of 89m,gNb in the 89Y(α, 4n) and 89Y(3He, 3n) reactions are higher than those in the 93Nb(γ, 4n) and natZr(p, xn) reactions, which indicates the role of input angular momentum. The isomeric-yield ratios of 89m,gNb in the 93Nb(γ, 4n), natZr(p, xn), 89Y(α, 4n), and 89Y(3He, 3n) reactions were also calculated theoretically using computer code TALYS 1.4. The theoretical isomeric-yield ratios of 89m,gNb from four reactions increase with excitation energy. However, the theoretical value are significantly higher than the experimental data in the 93Nb(γ, 4n) and natZr(p, xn) reactions but slightly lower or comparable in the 89Y(α, 4n) rand 89Y(3He, 3n) reactions. 相似文献
156.
Polyvinylimidazole/sol–gel composite as a novel solid‐phase microextraction coating for the determination of halogenated benzenes from aqueous solutions
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Manoochehr Farjaminezhad Mohammad Saber Tehrani Parviz Aberoomand Azar Syed Waqif Hussain Shahab Bohlooli 《Journal of separation science》2014,37(12):1475-1481
A polyvinylimidazole/sol–gel composite is proposed as a novel solid‐phase microextraction fiber to extract five halobenzenes from the headspace of aqueous solutions in combination with gas chromatography with mass spectrometry. The prepared fiber was characterized by scanning electron microscopy and Fourier transform infrared spectroscopy. The obtained results showed that porous polyvinylimidazole/sol–gel composite was chemically deposited on fused silica fiber. The effect of important extraction parameters including extraction temperature, extraction time, and salt content were investigated. The optimum conditions were as follows: extraction temperature 25°C, extraction time 20 min, and salt concentration 30 w/v%. Detection limits and relative standard deviations of the developed method for halogenated benzenes were below 0.1 pg/mL and 15%, respectively. Repeatability of the proposed method, explained by relative standard deviation, varied between 5.48 and 9.15% (n = 5). The limits of detection (S/N = 3) ranged between 0.01 and 0.10 ng/L using gas chromatography with mass spectrometry with selected ion monitoring mode. For real sample analysis, three types of water samples with different matrices (ground, surface, and tap water) were studied. The optimized procedure was applied to extraction and method validation of halogenated benzenes in spiked water samples. 相似文献
157.
Muhammad Imran Malik Tooba Mahboob Shakil Ahmed 《Analytical and bioanalytical chemistry》2014,406(25):6311-6317
Poly(2-vinylpyridine)s (P2VPs) are important polymers with extensive applications in modern day material science. P2VP is an exceptional case for liquid chromatography because of certain polar interactions with most of the stationary phases. In the present study, we established the critical adsorption point (CAP) of P2VP for the first time. The effectiveness of the method is demonstrated by analyses of blends and block copolymers of P2VP and PMMA. The CAP of PMMA is established for determination of molar mass of P2VP component of above mentioned blends and block copolymers. The methods successfully demonstrate the separation of both types of homopolymers from the rest of the samples in conjunction with the determination of molar mass distribution of noncritical block or component. Graphical Abstract
? 相似文献
158.
Muhammad Tariq Saqib Ali Muhammad Nawaz Tahir Nasir Khalid Jafir Hussain Shirazi 《Journal of the Iranian Chemical Society》2014,11(3):839-846
A series of six organotin(IV) carboxylates [Me2SnL2] (1), [n-Bu2SnL2] (2), [n-Oct2SnL2] (3), [Me3SnL] (4), n-Bu3SnL (5) and [Ph3SnL] (6), where L = 3-(4-cyanophenyl) acrylic acid have been synthesized and characterized by elemental analysis, FT-IR and NMR (1H, 13C). The complex (4) was also analyzed by single crystal X-ray analysis which showed distorted trigonal bipyramidal geometry with polymeric bridging behavior. The complexes 1–6 were screened for antimicrobial activities and cytotoxicity. The results showed significant activity with few exceptions. The catalytic activity of complexes was assessed in transesterification reaction of Brassica campestris oil (triglycerides) to produce biodiesel (fatty acid methyl esters). The results showed that triorganotin(IV) complexes exhibited good catalytic activity than their di-analogues. 相似文献
159.
Formation of the complex of ethyl viologen in its cationic (Ev+?) and neutral (Ev°) forms with β-cyclodextrin (β-CD) was investigated by means of voltammetric technique in buffer solution of pH 7.00. The number of βCD (n or m) per viologen species (Ev+?) or (Ev°), bonding equilibrium constants as well as bonding rate constants was calculated. The calculated values of $K_{\text{eq}}^{(1)}$ and $K_{\text{eq}}^{ ( 2)}$ (pertaining to the bonding of Ev+? and Ev° with βCD) are 13.6 M–n and 2.1 × 103 M?m , respectively, whereas the calculated values of n and m are 0.54 and 1.25, respectively. The bimolecular rate constant for the Ev°?βCD inclusion complex formation is 3.03 × 103 M?1s?1. These results are supported by the simulation of the experimental cyclic voltammograms. This study also highlights the significance of the proposed electrochemical method as compared to earlier studies on viologen-Cyclodextrin systems. 相似文献
160.
Yetkin Gök Senem Akkoç Mehmet Akkurt Muhammad Nawaz Tahir 《Journal of the Iranian Chemical Society》2014,11(6):1767-1774
The nine new heteroaryl-substituted imidazolidinium (1a–c), pyrimidinium (2a–c) and diazepinium (3a–c) salts as N-heterocyclic carbene (NHC) precursors were synthesized in good yields and entirely characterized using elemental analyses and conventional spectroscopic methods. In situ formed complexes from heterocyclic salts (1–3), Pd(OAc)2 and in the presence of KOBu t as a base were tested as catalysts for the Mizoroki–Heck coupling reaction in an aqueous media and very high yields were achieved. 1,3-Di(5-methylthiophen-2-ylmethyl)pyrimidinium hexafluorophosphate salt (2b) was structurally characterized by single-crystal X-ray diffraction. In the 2b compound (C16H21N2S2)+[PF6]?, the terminal thiophene rings are twisted with a dihedral angle of 72.8(3)°. In the pyrimidine ring, the three successive C atoms between the N atoms are disordered over two positions [occupancy ratio 0.753(12):0.247(12)]. In the crystal, neighboring molecules are linked by C–H…F hydrogen bonds, running along the b axis. 相似文献