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1.
JPC – Journal of Planar Chromatography – Modern TLC - The lipophilic character of phytol derivatives has been studied using reverse-phase planar chromatographic procedures.... 相似文献
2.
K. Meena K. Muthu M. Rajasekar V. Meenatchi S. P. Meenakshisundaram S. C. Mojumdar 《Journal of Thermal Analysis and Calorimetry》2013,112(2):1077-1082
Single crystals of tris(thiourea)silver(I) nitrate have been grown by slow evaporation solution growth technique from an aqueous solution at 25 °C. The single crystal X-ray diffraction study reveals that the crystal belongs to tetragonal system and cell parameters are a = b = 14.2790(4) Å, c = 24.8900(7) Å, and V = 5074.8(2) Å3. The various functional groups present in the molecule are confirmed by Fourier transformed infrared spectroscopy (FT-IR). The structure and the crystallinity of the materials were further confirmed by powder X-ray diffraction analysis. Thermogravimetric and differential thermal analysis reveal the purity of the sample and no decomposition is observed up to the melting point. The crystal is further characterized by UV–Vis and Vickers microhardness analysis. 相似文献
3.
Shreyans K. Jain Samdarshi Meena Asif K. Qazi Aashiq Hussain Sunil K. Bhola Rajendra Kshirsagar Koteppa Pari Anamika Khajuria Abid Hamid R. Uma Shaanker Sandip B. Bharate Ram A. Vishwakarma 《Tetrahedron letters》2013
The chromone alkaloid dysoline (1), a new regioisomer of rohitukine (2) along with rohitukine and rohitukine-N-oxide (3) were isolated from the stem barks of Dysoxylum binectariferum. The structure of dysoline (1) was determined by extensive 2D-NMR studies and the absolute configuration was established by NOESY and CD spectra. Dysoline (1) consisted of a 5,7-dihydroxy-2-methylchromone nucleus substituted with a 2′-hydroxylated N-Me piperidine ring at the C-6 position. Dysoline differs from rohitukine by the position of the piperidine ring on the chromone nucleus. Dysoline displayed promising cytotoxicity in HT1080 fibrosarcoma cells with an IC50 of 0.21 μM, and also displayed significant inhibition of proinflammatory cytokines TNF-α and IL-6. 相似文献
4.
Synthesis and Characterization of Silver–PVA Nanocomposite for Sensor and Antibacterial Applications
Silver–polyvinyl alcohol (PVA) nanocomposite is synthesized by a simple chemical reduction method in aqueous media and characterized by various techniques such as UV–Visible spectroscopy, transmission electron microscopy, X-ray diffraction and infrared spectroscopy. The morphology of the obtained silver nanoparticles is spherical in shape with an average diameter of 24 nm. The prepared silver–PVA nanocomposite is demonstrated to detect the concentration of heavy metal contaminant cadmium in water based on linear change in surface plasmon resonance absorption strength. The antibacterial tests show the inhibiting action of this nanocomposite against pathogenic bacteria Escherichia coli and Pseudomonas aeruginosa (gram negative), Bacillus cereus and Staphylococcus aureus (gram positive), which are found commonly in water. These observed optical and antibacterial properties, suggest the possible utilization of prepared silver–PVA nanocomposite in the water purification application. 相似文献
5.
Reactions of [ZnAl2(OPri)8] [A] with acetoxime in different molar ratios in refluxing anhydrous benzene, yield complexes of the type [ZnAl2(OPri)8?n{(CH3)2CNO}n] {where, n = 1–4}. All the complexes are transparent viscous/foamy solids. They were characterized by elemental analyses, FT-IR and NMR (1H, 13C {1H}) spectral studies. 27Al NMR spectrum of [ZnAl2(OPri)4{(CH3)2CNO}4] [4] in CDCl3 suggests presence of four coordination around both the aluminum atoms. IR spectra suggest that the oximato ligands bind the aluminum atoms in a side on manner in all the complexes. The ESI-mass spectrum of the representative derivative [4] suggests its monomeric nature while the thermo-gravimetric curve shows its low thermal stability. Sol–gel transformations of the precursors (A), (1), and (4) yielded nano-sized ZnAl2O4 samples (a), (b) and (c) at ~500 °C, respectively. The XRD patterns of (a), (b) and (c) indicate formation of cubic phase nano-sized zinc aluminate in all the samples. Surface morphologies of these samples were investigated by SEM images. IR spectra as well as EDX analyses indicate formation of pure zinc aluminate in all the cases. TEM image of sample (c) shows spherical (~5–8 nm) morphology. 相似文献
6.
Archana Chaudhary Ram Gopal Meena Nagar Rakesh Bohra 《Journal of Sol-Gel Science and Technology》2014,69(1):102-106
Some oxime modified complexes of the type [Zr{OPri}4?n{L}n] {where, n = 1–4 and LH=(CH3)2C=NOH (1–4) and C9H16C=NOH (5–8)} have been synthesized by the reaction of [Zr(OPri)4·PriOH] with oximes, in anhydrous refluxing benzene. These synthesized complexes were characterized by elemental analyses, molecular weight measurements, ESI-mass, FT-IR and NMR (1H and 13C{1H}) spectral studies. The ESI-mass spectral studies indicate dimeric nature for [Zr{OPri}2{ONC(CH3)2}2] (2), [Zr{OPri}3{ONC10H16}] (5) and [Zr{OPri}{ONC10H16}3] (7) and monomeric nature for [Zr{ONC10H16}4] (8). Oximato ligands appear to bind the zirconium in side on manner in all the complexes. Thermogravimetric curves of (2) and (8) exhibit multi-step decomposition with the formation of ZrO2, under nitrogen atmosphere. Sol–gel transformations of precursors (5), (6), (7) and (8) in organic medium, yielded nano-sized tetragonal phase of zirconia samples (a), (b), (c) and (d), respectively, on sintering at ~600 °C. All these samples were characterized by Powder XRD patterns and EDX analyses. Surface morphologies of these samples were investigated by SEM images. 相似文献
7.
A simple and efficient three-component procedure has been developed for the synthesis of a series of spiro-isoxazolo[5,4-b]pyridines/quinolines by one-pot condensation of isatins, 3-methylisoxazol-5-amine and enolizable cyclic carbonyl compounds. The protocol has been accomplished under solvent-free conditions by grinding the components at room temperature in presence of catalytic CH3COOH. The described process offers environmentally benign reaction conditions for the synthesis of pharmacologically important spirooxindole fused heterocycles with the advantages ofoperational simplicity, short reaction time and good to excellent yields of isolated pure product. 相似文献
8.
Mazaahir Kidwai Preeti Misra Bhavesh Dave Kumar R. Bhushan Rajendra K. Saxena Meena Singh 《Monatshefte für Chemie / Chemical Monthly》2000,17(3):1207-1212
A novel synthesis of 6-fluoro-7-(5-aryl-1,3,4-thiadiazol/oxadiazol-2-yl-sulfanyl)-4-quinolone-3-carboxylic acids from 7-chloro-6-fluoro-4-quinolone-3-carboxylic acid and 5-substituted 1,3,4-thiadiazoles/oxadiazoles on basic alumina under microwave activation is described. All compounds were screened for their in vitro antibacterial activity against B. lichenformis, 2689, K. aerogens 2281, S. typhimurium 2501, E. herbicola 2491, and P. vulgaris 2027 and found to possess activities comparable to that of the standard drug norfloxacin. 相似文献
9.
Low‐temperature sol–gel transformation of methyl silicon precursors to silica‐based hybrid materials
Veena Dhayal Rakesh Bohra Meena Nagar Ajay Kaushik Sanjay Mathur Sven Barth 《应用有机金属化学》2008,22(11):629-636
Six new methyl silicon (IV) precursors of the type [MeSi{ON?C(R)Ar}3] [when R = Me, Ar = 2‐C5H4N ( 1 ), 2‐C4H3O ( 2 ) or 2‐C4H3S ( 3 ); and when R = H, Ar = 2‐C5H4N ( 4 ), 2‐C4H3O ( 5 ) or 2‐C4H3S ( 6 )] were prepared and structurally characterized by various spectroscopic techniques. Molecular weight measurements and FAB (Fast Atomic Bombardment) mass spectral studies indicated their monomeric nature. 1H and 13C{1H} NMR spectral studies suggested the oximate ligands to be monodentate in solution, which was confirmed by 29Si{1H} NMR signals in the region expected for tetra‐coordinated methylsilicon (IV) derivatives. Thermogravimetric analysis of 1 revealed the complex to be thermally labile, decomposing to a hybrid material of definite composition. Two representative compounds ( 2 and 4 ) were studied as single source molecular precursor for low‐temperature transformation to silica‐based hybrid materials using sol–gel technique. Formation of homogenous methyl‐bonded silica materials (MeSiO3/2) at low sintering temperature was observed. The thermogravimetric analysis of the methylsilica material indicated that silicon‐methyl bond is thermally stable up to a temperature of 400 °C. Reaction of 2 and Al(OPri)3 in equimolar ratio in anhydrous toluene yielded a brown‐colored viscous liquid of the composition [MeSi{ON?C(CH3)C4H3O}3.Al(OPri)3]. Spectroscopic techniques 1H, 13C{1H}, 27Al{1H} and 29Si{1H} NMR spectra of the viscous product indicated the presence of tetracoordination around both silicon and aluminum atoms. On hydrolysis it yielded methylated aluminosilicate material with high specific surface area (464 m2/g). Scanning electron micrography confirmed a regular porous structure with porosity in the nanometric range. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
10.