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41.
Susanta Hazra Samit Majumder Michel Fleck Núria Aliaga-Alcalde Sasankasekhar Mohanta 《Polyhedron》2009,28(17):3707-3714
Synthesis, molecular and supramolecular structures, electrochemistry and magnetic properties of two diphenoxo-bridged dicopper(II) compounds [CuII2L(H2O)(ClO4)]·ClO4·2H2O (1) and [CuII2L(N3)2]·2H2O (2) derived from a tetraimino diphenolate macrocyclic ligand H2L, obtained on [2+2] condensation of 4-methyl-2,6-diformylphenol and 2,2′-dimethyl-1,3-diaminopropane, are presented. Supramolecular structure of both 1 and 2 are three-dimensional resulting from hydrogen bonding interactions. Interestingly, the 3-D self-assembly of 2 contains micropores having the dimension of 0.35 nm. Electrochemical analyses reveal that both of these compounds exhibit two-step couples in the reduction window. Variable-temperature (2–300 K) magnetic susceptibilities measurements of the two compounds reveal that the metal centers in both of the complexes are coupled by strong antiferromagnetic interactions with J values (H = ?JS1·S2) ?776 and ?836 cm?1 for 1 and 2, respectively. 相似文献
42.
Low levels of water (limit of detection 2-5 mg kg1?)can be determined in a non-polar organic solvents such as benzene, 1,2-dichloroethane (DCE) and n-hexane by utilizing the reaction of water with SnCl4 or SbCl5. The reaction results of hydrolysis in halide and is accompanied by a decrease in optical absorption. With SnSl4, the reaction is monitored near 300 nm and with SbCl5 it is monitored at lower wavelengths (350-420). Niether reactons proceeds well in media containing only DCE and n-hexane. For this reason, the arrangemens involves a halide reagent dissolved in benzene which is merged with a benzene/n-hexane/DCE carrier stream into which samlpe is injected. A configuration in which only 2μl of a concentrated halide reagent solution is injected into the flowing sample stream is also shown to be viable for the determination of water in benzene. A membrane-permeation-based calibration method for preparing trace water standards is described. 相似文献
43.
Banerjee K Dasgupta S Jadhav MR Naik DG Ligon AP Oulkar DP Savant RH Adsule PG 《Journal of AOAC International》2010,93(6):1957-1964
An analytical method is reported for residue analysis of the fungicide meptyldinocap in different fruit matrixes that involves extraction with ethyl acetate, hydrolysis of the residues with ethanolamine, and determination by LC/MS/MS. The method involves extraction of 10 g sample with 10 mL ethyl acetate; evaporation of the ethyl acetate phase to dryness, and subsequent hydrolysis of the residues to 4,6-dinitro-2-(1-methylheptyl) phenol on reaction with 1% ethanolamine. The pH of this hydrolyzed product was neutralized with formic acid and analyzed by LC/MS/MS. The hydrolysis reaction followed pseudo-first-order kinetics, and the reaction product was spectroscopically confirmed as 2-(1-methylheptyl)-4,6-dinitrophenol. The method offered > 80% recoveries at an LOQ of 10 ng/g for grape and mango, 25 ng/g for pomegranate with intralaboratory Horwitz ratio < 0.5, and measurement uncertainties < 10% at LOQ levels. Considering first-order rate kinetics, activation energy, enthalpy of activation, and entropy of activation varied as solvent > mango > grape > pomegranate. Free energy of activation at 298 K was higher than at 280 K and was similar for solvent and three matrixes at both temperatures. 相似文献
44.
Sounak Dutta Dibyendu Das Antara Dasgupta Prasanta Kumar Das Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(5):1493-1505
The gelation of ionic liquids is attracting significant attention because of its large spectrum of applications across different disciplines. These ‘green solvents’ have been the solution to a number of common problems due to their eco‐friendly features. To expand their applications, the gelation of ionic liquids has been achieved by using amino acid‐based low‐molecular‐weight compounds. Variation of individual segments in the molecular skeleton of the gelators, which comprise the amino acid and the protecting groups at the N and C termini, led to an understanding of the structure–property correlation of the ionogelation process. An aromatic ring containing amino acid‐based molecules protected with a phenyl or cyclohexyl group at the N terminus were efficient in the gelation of ionic liquids. In the case of aliphatic amino acids, gelation was more prominent with a phenyl group as the N‐terminal protecting agent. The probable factors responsible for this supramolecular association of the gelators in ionic liquids have been studied with the help of field‐emission SEM, 1H NMR, FTIR, and luminescence studies. It is the hydrophilic–lipophilic balance that needs to be optimized for a molecule to induce gelation of the green solvents. Interestingly, to maximize the benefits from using these green solvents, these ionogels have been employed as templates for the synthesis of uniform‐sized TiO2 nanoparticles (25–30 nm). Furthermore, as a complement to their applications, ionogels serve as efficient adsorbents of both cationic and anionic dyes and were distinctly better relative to their organogel counterparts. 相似文献
45.
Detection and analysis of paraffin oil adulteration in coconut oil using fiber optic long period grating sensor 总被引:1,自引:0,他引:1
A fiber optic sensing system for the detection of adulteration of coconut oil by paraffin oil is experimentally demonstrated. The sensing mechanism is based on the sensitive dependence of the resonance peaks of a long period grating (LPG) on the changes of the refractive index of the environmental medium surrounding the cladding surface of the grating. The wavelength shift of the attenuation bands of the LPG was measured with the sensor immersed in a mixture of paraffin oil and pure coconut oil in different proportions. Detection limit of adulteration was found to be 3% for coconut oil-paraffin oil binary mixture. 相似文献
46.
du Rietz R Hinde DJ Dasgupta M Thomas RG Gasques LR Evers M Lobanov N Wakhle A 《Physical review letters》2011,106(5):052701
The inhibition of fusion by quasifission is crucial in limiting the formation of superheavy elements in collisions of heavy nuclei. Time scales of ~10(-18) s inferred for fissionlike events from recent crystal blocking measurements were interpreted to show either that quasifission itself is slower than previously believed, or that the fraction of slow fusion-fission is higher than expected. New measurements of mass-angle distributions for (48)Ti and (64)Ni bombarding W targets show that in these reactions quasifission is the dominant process, typically occurring before the system formed after contact has made a single rotation, corresponding to time scales of ≤10(-20) s. 相似文献
47.
Dattatray J. Late Mahendra A. More Sucharita Sinha K. Dasgupta Pankaj Misra B. N. Singh Lalit M. Kukreja Sudha V. Bhoraskar Dilip S. Joag 《Applied Physics A: Materials Science & Processing》2011,104(2):677-685
The paper deals with the comparative study of nanocrystalline Lanthanum hexaboride (LaB6) thin films grown on various substrates by Pulsed laser deposition and Arc plasma method. Field emission studies were carried
out on LaB6 films deposited on various substrates show metallic behavior of the emitters. The high value of field enhancement factors,
indicating that the electron emission from LaB6 nanoscale protrusions deposited on emitter surface. The post field emission surface morphology of the emitters showed no
significant erosion of the films during continuous operation. The observed behavior indicates that it is linked with the growth
of LaB6 films on substrate crystal structure. The LaB6 nanocrystallites/nanowires films were synthesized using arc plasma method shows good emission current stability. The LaB6 micro/nanocrystallites were also obtained by picosecond laser irradiation which gives high enhancement β factor, and good emission current stability along with high current density. The results reveal that nanocrystalline LaB6 films, exhibit high resistance to ion bombardment and excellent structural stability and are more promising emitters for
practical applications in field emission based new generation devices. 相似文献
48.
M Dasgupta D J Hinde R D Butt A C Berriman C R Morton J O Newton K Hagino 《Pramana》1999,53(3):513-520
The availability of precisely measured fusion excitation functions have allowed the determination of experimental fusion barrier
distributions. This concept is utilised in 9Be+208Pb reaction, to reliably predict the expected complete fusion cross-sections. However, the measured cross-sections are found
to be only 68% of those predicted. The large cross-sections observed for incomplete fusion products support the interpretation
that this suppression of fusion is caused by 9Be breaking up into charged fragments before reaching the fusion barrier. 相似文献
49.
Sawalha MF Sengupta MK Ohira S Idowu AD Gill TE Rojo L Barnes M Dasgupta PK 《Talanta》2008,77(1):372-379
A gas phase chemiluminescence (GPCL)-based method for trace measurement of arsenic has been recently described for the measurement of arsenic in water. The principle is based on the reduction of inorganic As to AsH3 at a controlled pH (the choice of pH governs whether only As(III) or all inorganic As is converted) and the reaction of AsH3 with O3 to produce chemiluminescence (Idowu et al., Anal. Chem. 78 (2006) 7088-7097). The same general principle has also been used in postcolumn reaction detection of As, where As species are separated chromatographically, then converted into inorganic As by passing through a UV photochemical reactor followed by AsH3 generation and CL reaction with ozone (Idowu and Dasgupta, Anal. Chem. 79 (2007) 9197-9204). In the present paper we describe the measurement of As in different soil and dust samples by serial extraction with water, citric acid, sulfuric acid and nitric acid. We also compare parallel measurements for total As by induction coupled plasma mass spectrometry (ICP-MS). As(V) was the only species found in our samples. Because of chloride interference of isobaric ArCl+ ICP-MS analyses could only be carried out by standard addition; these results were highly correlated with direct GPCL and LC-GPCL results (r2 = 0.9935 and 1.0000, respectively). The limit of detection (LOD) in the extracts was 0.36 μg/L by direct GPCL compared to 0.1 μg/L by ICP-MS. In sulfuric acid-based extracts, the LC-GPCL method provided LODs inferior to those previously observed for water-based standards and were 2.6, 1.3, 6.7, and 6.4 μg/L for As(III), As(V), dimethylarsinic acid (DMA) and monomethylarsonic acid (MMA), respectively. 相似文献
50.
Jyotirmoy Chakravarty Rupak Dasgupta Jayanta K Ray Usha R Ghatak 《Proceedings Mathematical Sciences》1977,86(3):317-325
The gross structures of the cyclised products from the acid-catalysed cyclisations of 2-benzyl-1, 3-dimethylcyclohexanol (6) and 1-benzyl-3, 5-dimethylcyclohexanol (11) revealing the influence of the structure of the benzylcyclohexanol derivative, and of the cyclisation reagent, have been evaluated. Polyphosphoric acid and aluminium chloride catalysed cyclisations of (6) result in the formation of predominantly 1, 4a-dimethyl-1, 2, 3, 4, 4a, 9a-hexahydrofluorene (7) and 4, 9-dimethyl-7, 8-benzobicyclo [3.3.1] non-7-ene (9) respectively. Under the same conditions, (11) produced cyclised products consisting mostly the benzobicyclo [3.3.1] non-7-ene derivative (12), characterised through 1,3-dimethyl-7,8-benzobicyclo [3.3.1] non-6-oxo-7-ene (14) by oxidation with chromium trioxide. Phosphorus pentoxide induced cyclisation of (6), followed by oxidation gave a mixture of the bridged-ring ketone (10) and the 9-oxohydrofluorene (8) in a ratio ofca. 3 : 2, whereas 2-benzyl-5-methylcyclohexanol (19) resulted in mostly 2-methyl-7,8-benzobicyclo [3.3.1] non-6-oxo-7-ene (19). 相似文献