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1.
We have presented an investigation of the induced focusing in Kerr media of two laser beams, the pump beam and the probe beam,
which could be either Gaussian or elliptic Gaussian or a combination of the two. We have used variational formalism to derive
relevant beam-width equations. Among several important findings, the finding that a very week probe beam can be guided and
focused when power of both beams are well below their individual threshold for self-focusing, is a noteworthy one. It has
been found that induced focusing is not possible for laser beams of any wavelength and beam radius. In case both beams are
elliptic Gaussian, we have shown that when power of both beams is above a certain threshold value then the effective radius
of both beams collapses and collapse distance depends on power. Moreover, it has been found that induced focusing can be employed
to convert a circular Gaussian beam into an elliptic Gaussian beam. 相似文献
2.
So-Yon Lim Matt Meyer Richard A Kjonaas Swapan K Ghosh 《Journal of immune based therapies and vaccines》2007,5(1):3-1
This is a correction article. 相似文献
3.
Breathers in discrete nonlinear ferrimagnetic spin lattices are investigated for both easy-axis and easy-plane configurations.
The region in frequency space of the formation of breathers is determined and the anticontinuum limit discussed. The monochromatic
and the coloured breathers are found out numerically for different parameters and different conditions of excitations. 相似文献
4.
J.S. Yadav B.V. Subba Reddy P. Vishnumurthy Swapan Kr. Biswas 《Tetrahedron letters》2007,48(38):6641-6643
α-Diazoketones undergo smooth allylation with successive bromide insertion with allylindium bromide generated in situ from allyl bromide and indium metal to produce 1-bromo-2-alkyl- or 2-arylpent-4-en-2-ols in high yields. Addition of propargylindium bromide produces 1-bromo-2-alkyl-or 2-arylpent-4-yn-2-ols under similar conditions. 相似文献
5.
Dinabandhu Pramanick Jyotish Sarkar Ramanath Bhattacharyya 《Journal of polymer science. Part A, Polymer chemistry》1988,26(5):1457-1463
The reactions of OH radical with Cl?, Br?, I?, and F? ions have been studied by entrapping the product radicals as polymer endgroup which have been detected and estimated by the sensitive dye partition technique. The rate constants of the reactions with Br?, Cl?, and F? ions have been determined to be 1.51 × 109, 1.32 × 109, and 0.92 × 109 L mol?1 s?1, respectively at 25°C and pH 1.00. Oxidation of I? ions liberates I, which inhibits the polymerization and the reaction could not be followed by polymer endgroup analysis. The observed order of reactivity Br? > Cl? > F? is in accordance with the electron affinities of the halide ions. The acidity of the reaction medium has a strong influence on the rate of reaction. With Br? ions, the rate constant of the reaction falls from 1.51 × 109 to 0.75 × 109 L mol?1 s?1 at 25°C as the pH is raised from 1.0 to 2.8. The method is simple and accurate and can be applied to study very reactive radicals. 相似文献
6.
In search for a cheaper anode catalyst for the oxidation of ethanol for development of direct alcohol fuel cells, Pd has been
considered here as an interesting substitute for Pt in Pt Ru binary electrodeposite. The binary catalyst when co-deposited
on nickel support has been found to increase the current density and decrease the anodic overvoltage significantly with respect
to pure Pt, Pd and Ni. Its electrocatalytic capability is also comparable with that of the Pt-Ru binary electrocatalyst on
Ni-support, when studied in 1 M EtOH containing 1 M NaOH solution. The effect of loading of Pd Ru electrocatalyst on Ni support has also been tested. The electrocatalytic activity
of the electrodes for oxidation of ethanol has been explained by studies of cyclic voltammetry, chronopotentiometry, steady-state
polarization, and conjugated scanning electron microscopy–energy dispersion X-ray spectroscopy. It has been found that electrode
containing the higher amount of deposit are less affected by carbonaceous poisons. 相似文献
7.
Summary The kinetics of reduction of [MnIII(cydta)]– (where H4cydta=trans-cyclohexane-1,2-diamine-N N N' N'-tetraacetic acid) by some thiourea reductants have been studied in aqueous solution by stopped-flow techniques in the pH ranges 2.5–4.5 and 9.2–10.2. An initial increase in absorbance followed by a steady decrease indicated the formation of a precursor complex prior to the electron transfer step. The reactions are first order in both oxidant and reductant. The observed increase in rate in going from low to high pH is attributed to the difference in reactivities of the aqua and hydroxo species of the MnIII complex; the higher reactivity of the latter is consistent with the formation of a ligand-bridged activated species prior to electron transfer. The reactivity order for the thiourea derivatives follows the order of their reported substituent effects. 相似文献
8.
A new crystal-engineering motif has been developed where a ditopic receptor 1 shows a novel syn-syn hydrogen-bonded polymeric supramolecular complex (Fig. 4b) (instead of a 1:1 dimeric syn-syn or polymeric syn-anti complex) giving rise to a hydrogen-bonded stair-like polymeric ribbon structure between the binding groups of the receptor pyridine amide and the carboxyl groups of the guest substrate. 相似文献
9.
D. Pramanick A. K. Chatterjee 《Journal of polymer science. Part A, Polymer chemistry》1980,18(8):2585-2595
Ceric-thiol systems are good initiators for the acid aqueous polymerization of some water-soluble Vinyl monomers although not for styrene (in aqueous emulsion) and vinyl acetate. Thiols used are 2-mercaptoethanol, thioglycolic acid, 2-mercaptoethylamine hydrochloride, and L -cysteine hydrochloride. The polymerization proceeds through a radical mechanism. End-group analysis of poly(methyl methacrylate) obtained by initiation with various ceric-thiol systems has been carried out using Palit's dye testes. Hydroxyl, carboxyl, and amine end groups (to the extent of about one per polymer molecule) were incorporated in poly(methyl methacrylate)s obtained by initiation with 2-mercaptoethanol, thioglycolic acid, and 2-mercaptoethylamine hydrochloride, respectively, each in combination with Ce4+ ions; both amine and carboxyl end groups were obtained using C4+/L -cysteine hydrochloride initiator system. From the end-group results, the initiating species have been identified and the initiation mechanism prooposed. The probable termination mechanism also has been discussed. 相似文献
10.
Chain transfer involving thiourea in radical polymerization of methyl methacrylate in acidic aqueous media has been studied by polymer endgroup analysis using the dye-partition technique. Thiourea has feeble reactivity in chain transfer, the transfer constant with respect to poly (methyl methacrylate) radicals being 1.21 × 10?4 at 42°. This chain transfer study led to the development of a new method for studying the tautomeric equilibrium between the thione and thiol forms of thiourea. The equilibrium is pH dependent and the equilibrium constant at 42° is 232. The ratios of the equilibrium concentrations of the thiol to thione forms of thiourea at various pH's have been calculated. The thiol form is responsible for the chain transfer reactivity; it predominates in strongly acidic media and is almost absent above pH 3.5. This new method may be used for studying the thione-thiol tautomerism of other thiourea derivates. 相似文献