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991.
Petroselli G Mandal MK Chen LC Ruiz GT Wolcan E Hiraoka K Nonami H Erra-Balsells R 《Journal of mass spectrometry : JMS》2012,47(3):313-321
A group of rhenium (I) complexes including in their structure ligands such as CF(3)SO(3)-, CH(3)CO(2)-, CO, 2,2'-bipyridine, dipyridil[3,2-a:2'3'-c]phenazine, naphthalene-2-carboxylate, anthracene-9-carboxylate, pyrene-1-carboxylate and 1,10-phenanthroline have been studied for the first time by mass spectrometry. The probe electrospray ionization (PESI) is a technique based on electrospray ionization (ESI) that generates electrospray from the tip of a solid metal needle. In this work, mass spectra for organometallic complexes obtained by PESI were compared with those obtained by classical ESI and high flow rate electrospray ionization assisted by corona discharge (HF-ESI-CD), an ideal method to avoid decomposition of the complexes and to induce their oxidation to yield intact molecular cation radicals in gas state [M](+·) and to produce their reduction yielding the gas species [M](-·). It was found that both techniques showed in general the intact molecular ions of the organometallics studied and provided additional structure characteristic diagnostic fragments. As the rhenium complexes studied in the present work showed strong absorption in the UV-visible region, particularly at 355?nm, laser desorption ionization (LDI) mass spectrometry experiments could be conducted. Although intact molecular ions could be detected in a few cases, LDI mass spectra showed diagnostic fragments for characterization of the complexes structure. Furthermore, matrix-assisted laser desorption ionization (MALDI) mass spectra were obtained. Nor-harmane, a compound with basic character, was used as matrix, and the intact molecular ions were detected in two examples, in negative ion mode as the [M](-·) species. Results obtained with 2-[(2E)-3-(4-tert-buthylphenyl)-2-methylprop-2-enylidene] malononitrile (DCTB) as matrix are also described. LDI experiments provided more information about the rhenium complex structures than did the MALDI ones. 相似文献
992.
Suman Kumar Saha Rajib Kar Durbadal Mandal Sakti Prasad Ghoshal 《Memetic Computing》2013,5(4):311-321
In this paper, a new optimization method named gravitational search algorithm (GSA) is adopted for designing optimal linear phase finite impulse response band pass (BP) and band stop (BS) digital filters. Other various population based evolutionary algorithms like real coded genetic algorithm, conventional particle swarm optimization, differential evolution (DE), bee swarm optimization have also been applied for the sake of comparative study of the same optimal designs. In GSA, particles are considered as objects and their performances are measured by their masses. All these objects attract each other by gravity forces, and these forces produce global movements of all objects towards the objects with heavier masses. GSA guarantees the exploitation step of the algorithm and it is apparently free from premature convergence. Extensive simulation results justify superior optimization capability of GSA over the afore-mentioned optimization techniques for the solution of the multimodal, non-differentiable, highly non-linear, and constrained filter design problems. 相似文献
993.
Sangeeta Mondal Sakti Prasad Ghoshal Rajib Kar Durbadal Mandal 《Journal of Optimization Theory and Applications》2012,155(1):315-324
This paper proposes one novel algorithm called differential evolution with wavelet mutation for the optimal design of linear phase finite impulse response filters. For comparative performance study, the Parks–McClellan algorithm and some evolutionary algorithms like the real coded genetic algorithm, conventional particle swarm optimization, and conventional differential evolution have also been applied. 相似文献
994.
Optical nonlinear materials have been used for several digital logic and arithmetic operations. These operations are conducted in real time domain as per their operational speed is concerned. In this paper authors propose a new method of all optical half adder scheme. This type of switching is based on polarization properties of light along with nonlinear properties of material. As the state of polarization of light ensures that the field intensity level of the light signal is the same in whole operation, the scheme may be extended to some wide applications in all optical parallel computation and information processing. 相似文献
995.
Bi1–xBaxFeO3 (0.0≤x≤0.25) ceramics are prepared by chemical synthesis route. At room temperature, antiferromagnetic BiFeO3 is converted to ferromagnetic on doping Ba. A large change in the magnetization is observed around 370 °C which is close to the Neel temperature (TN) of parent compound. Another magnetic transition is also observed near 600 °C. Spin canting or impurity phase could be a probable reason for the origin of ferromagnetism in both cases. Ferroelectric and magnetic transitions of the compounds shift towards higher temperature with Ba-doping concentration. Anomaly in the dielectric constant is also observed near the TN of BiFeO3. The composition x=0.15 shows the maximum magnetic moment at room temperature while better fatigue resistance and maximum magnetoelectric coupling are observed for x=0.20 composition. 相似文献
996.
Drozd M Baran J 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2006,64(4):867-879
Polarised IR-microscope spectra of C(NH(2))(3)*HSO(4) small single crystal samples were measured at room temperature. The spectra are discussed on the basis of oriented gas model approximation and group theory. The stretching nuOH vibration of the hydrogen bond with the Ocdots, three dots, centeredO distance of 2.603A gives characteristic broad AB-type absorption in the IR spectra. The changes of intensity of the AB bands in function of polariser angle are described. Detailed assignments for bands derived from stretching and bending modes of sulphate anions and guanidinium cations were performed. The observed intensities of these bands in polarised infrared spectra were correlated with theoretical calculation of directional cosines of selected transition dipole moments for investigated crystal. The vibrational studies seem to be helpful in understanding of physical and chemical properties of described compound and also in design of new complexes with exactly defined behaviors. 相似文献
997.
Samaddar S Mandal AK Mondal SK Sahu K Bhattacharyya K Roy S 《The journal of physical chemistry. B》2006,110(42):21210-21215
The nature of solvent molecules around proteins in native and different non-native states is crucial for understanding the protein folding problem. We have characterized two compact denatured states of glutaminyl-tRNA synthetase (GlnRS) under equilibrium conditions in the presence of a naturally occurring osmolyte, l-glutamate. The solvation dynamics of the compact denatured states and the fully unfolded state has been studied using a covalently attached probe, acrylodan, near the active site. The solvation dynamics progressively becomes faster as the protein goes from the native to the molten globule to the pre molten globule to the fully unfolded state. Anisotropy decay measurements suggest that the pre-molten-globule intermediate is more flexible than the molten globule although the secondary structure is largely similar. Dynamic light scattering studies reveal that both the compact denatured states are aggregated under the measurement conditions. The implications of solvation dynamics in aggregated compact denatured states have been discussed. 相似文献
998.
Swadhin K. Mandal 《Journal of organometallic chemistry》2006,691(13):2969-2977
The chemistry of η3-allyl palladium complexes of the diphosphazane ligands, X2PN(Me)PX2 [X = OC6H5 (1) or OC6H3Me2-2,6 (2)] has been investigated.The reactions of the phenoxy derivative, (PhO)2PN(Me)P(OPh)2 with [Pd(η3-1,3-R′,R″-C3H3)(μ-Cl)]2 (R′ = R″ = H or Me; R′ = H, R″ = Me) give exclusively the palladium dimer, [Pd2{μ-(PhO)2PN(Me)P(OPh)2}2Cl2] (3); however, the analogous reaction with [Pd(η3-1,3-R′,R″-C3H3)(μ-Cl)]2 (R′ = R″ = Ph) gives the palladium dimer and the allyl palladium complex [Pd(η3-1,3-R′,R″-C3H3)(1)](PF6) (R′ = R″ = Ph) (4). On the other hand, the 2,6-dimethylphenoxy substituted derivative 2 reacts with (allyl) palladium chloro dimers to give stable allyl palladium complexes, [Pd(η3-1,3-R′,R″-C3H3)(2)](PF6) [R′ = R″ = H (5), Me (7) or Ph (8); R′ = H, R″ = Me (6)].Detailed NMR studies reveal that the complexes 6 and 7 exist as a mixture of isomers in solution; the relatively less favourable isomer, anti-[Pd(η3-1-Me-C3H4)(2)](PF6) (6b) and syn/anti-[Pd(η3-1,3-Me2-C3H3)(2)](PF6) (7b) are present to the extent of 25% and 40%, respectively. This result can be explained on the basis of the steric congestion around the donor phosphorus atoms in 2. The structures of four complexes (4, 5, 7a and 8) have been determined by X-ray crystallography; only one isomer is observed in the solid state in each case. 相似文献
999.
Mallick A Mandal MC Haldar B Chakrabarty A Das P Chattopadhyay N 《Journal of the American Chemical Society》2006,128(10):3126-3127
Tuning of the sensory capability of a potentially bioactive indoloquinolizine system, namely, 3-acetyl-4-oxo-6,7-dihydro-12H-indolo-[2,3-a]-quinolizine (AODIQ), is described in a biomimicking micellar nanocage. It has been shown that surfactant concentration dictates the sensing behavior of the fluorophore toward physiologically essential trace metals, such as Cu2+. This is a simple, efficient, and general technique that allows one to utilize the sensor to its maximum efficiency. 相似文献
1000.
Perchloric acid adsorbed on silica-gel (HClO4-SiO2) was found to be a new, highly efficient, inexpensive and reusable catalyst for chemoselective N-tert-butoxycarbonylation of amines at room temperature and under solvent-free conditions. 相似文献