Propagation of sound pulses in a semiinfinite stratified medium

We consider the propagation of sound pulses due to a line source in the inhomogeneous, semi-infinite mediumy ≥ 0 with the boundary conditionφ=0 or?φ/(?y)=0 aty=0, whereφ is the acoustic velocity potential. We suppose that the velocity of wave propagation,c, is given byc ^?2=p ?qe ^?ay , wherep, q, α are real and positive andp>q. The method of dual integral transformation is used. The solution in terms of pulse propagation modes yields the diffracted pulse and the method of steepest descents gives the geometrical acoustic field.     

Kelvin Helmholtz Instability in a Magnetoplasma

Two dimensional transverse Kelvin-Helmholtz (K-H) instability has been studied at the interface between the two fluids (plasma medium) of finite thickness in relative motion to each other. The perturbations on the interface are assumed to be electromagnetic and a dispersion relation is obtained. The interface (boundary) has been found to be unstable for a wide range of perturbation wavelengths (wave numbers kx, ky). It is shown that the modification introduced by electromagnetic (quasi-electrostatic) perturbations in comparison to electrostatic one is to reduce the growth rate of perturbations. The growth rate maximizes when kx = ky. The applications of this study have been discussed to explain some of the observed ionospheric (auroral arc formation) and magnetospheric (unstable magnetopause boundary, hydromagnetic pulsations) phenomena.     

Raman and infrared spectra of tere-phthalaldehyde

The laser Raman spectrum of tere-phthalaldehyde powder has been recorded on a Jobin Yvonhg 2S spectrophotometer with a~100 mW Argon-Ion laser. The infrared spectrum of the solid substance has been recorded on a Perkin-Elmer 621 spectrophotometer in the region 300–4000 cm^-1 using KBr and nujol mull techniques. The observed frequencies have been assigned in terms of the fundamentals, overtones and combinations assumingD _2h point-group symmetry.     

Valence transition and magnetic ordering in Sn doped EuPd2Si2

The sharp, temperature induced, continuous valence transition in EuPd₂Si₂ is drastically changed by doping with Sn at the Si site upto 5 at. %. Only a first order valence transition occurs for a 3% Sn doped sample and the 2⁺ component which survives the valence transition orders magnetically at 4.2 K. No valence transition at all occurs for a 5% Sn doped sample right up to 1.9 K and magnetic ordering sets in around 30 K.     

The interplay of hydrophobic and electrostatic effects in the surfactant-induced aggregation/deaggregation of chlorin p6

The aggregation/deaggregation of chlorin p6 with the surfactants CTAB, SDS, and TX 100 have been studied by using absorption, fluorescence, and light scattering techniques. The ionic surfactants are found to cause aggregation of fluorophore at submicellar concentrations. The aggregates dissolve at higher surfactant concentrations to yield micellized monomers. This is rationalized by the interplay of electrostatic and hydrophobic effects. A prominent pH effect is observed in the ionic surfactant induced aggregation process as the charge on the fluorophore is controlled by the pH of the medium. Interestingly, the neutral TX-100 also induces aggregation of chlorin p6 at low concentrations, indicating that hydrophobic effects by themselves can cause aggregation unless there is a hindrance by repulsive electrostatic effects.     

Total synthesis of carbazoquinocin C: application of the o-benzannulation of Fischer carbene complexes to carbazole-3,4-quinone alkaloids

[reaction: see text] The photoinduced o-benzannulation of 3-(2-vinyl)indolylcarbene complexes provides a direct route to carbazole derivatives that are oxygenated in the 3- and 4-positions. This reaction is quite efficient and provides for a unique synthesis of the lipid peroxidation inhibitor carbazoquinocin C.     

Quantitative detection of singlet O2 by cavity-enhanced absorption

A method for the practical determination of the absolute concentration of single (a1delta(g)) oxygen is discussed. The method is based on sensitive off-axis integrated-cavity-output spectroscopy (ICOS). Off-axis ICOS allows narrowband, continuous-wave lasers to be used in conjunction with optical cavities to record sensitive absorption measurements. The details of the method as well as spectroscopic data confirming the first observation of the (1, 0) band of the b1sigma(g)(+) - a1delta(g) Noxon system are presented. The absolute transition probabilities for the b1sigma(g)(+) - a1delta(g) Noxon system, which are not known precisely from experiments, are determined by quantum chemistry theory.     

Measurement of two-photon absorption cross-section in organic molecular salt with linear and circular polarized radiation

We report on the investigation of two-photon absorption (TPA) in 4-Diethylamino-N-Methyl-4-Stilbazolium Tosylate (DEST) with 40 picosecond, 1064 nm linear and circular polarization laser radiation. The TPA cross-section ₂ measured is larger for linear polarized radiation (948 GM) than that for the circular polarized radiation (840 GM). The large TPA cross-section of DEST facilitates highly directional and efficient TPA induced upconverted emission in the range of 590–640 nm even though the fluorescence efficiency of DEST is very low (0.5%). The net single pass efficiency of upconversion is 7%. PACS 42.65.-k; 42.70.Jk     

Enzymatic synthesis of oligosaccharides, alkyl and terpenyl glucosides, by recombinant Escherichia coli-expressed Pichia etchellsii β-glucosidase II

The biosynthetic activity of yeast Pichia etchellsii β-glucosidase II (BglII) expressed in recombinant Escherichia coli was utilized for synthesis of cellooligosaccharides, alkyl and terpene glucosides. Cellooligosaccharides with a degree of polymerization of 3 and greater were resolved by thin-layer chromatography (TLC) using an ethyl acetate: 1-propanol:2-propanol:water (8:5:1:1) solvent system followed by visualization with 0.2% naphthoresorcinol reagent. Using 2M cellobiose and 15 IU of partially purified BglII, 57 mmol/L of oligosaccharides (comprising mostly cellotriose and cellopentaose) was synthesized in 16 h. Similarly, alkyl glucosides with chain lengths from 6 to 10 carbons were synthesized and products extracted to near purity by ethylacetate extraction. The same extraction method was employed to separate, to near purity, various monoterpenyl (nerol, geraniol, citronellol) glucosides. A reliable and simple method for separation of cellooligosaccharides using a combination of Bio-Gel P-2 gel filtration and charcoal celite adsorption chromatography was developed. The cellooligosaccharides were separated to purity as confirmed by TLC. The enzyme was among the very few that could synthesize a wide variety of glycoconjugates.     

Measurements of F2 and xF(nu)(3) - xF(nu;)(3) from CCFR nu(mu)-Fe and nu;(mu)-Fe Data in a Physics Model-Independent Way

We report on the extraction of the structure functions F2 and DeltaxF(3) = xF(nu)(3)-xF(nu;)(3) from CCFR nu(mu)-Fe and nu;(mu)-Fe differential cross sections. The extraction is performed in a physics model-independent (PMI) way. This first measurement of DeltaxF(3), which is useful in testing models of heavy charm production, is higher than current theoretical predictions. The ratio of the F2 (PMI) values measured in nu(mu) and mu scattering is in agreement (within 5%) with the predictions of next-to-leading-order parton distribution functions using massive charm production schemes, thus resolving the long-standing discrepancy between the two sets of data.