Differential oscillator strengths and dipole polarizabilities for transitions of the helium sequence

The dipole radial integral for an initial discrete 1s state and a final continuum state has been calculated under the screened hydrogenic model. In this model, single-electron hydrogenic wave functions are employed and the initial and the final states are treated by two different effective-charge parameters. Numerical values of differential oscillator strengths for transitions from 1s 21S to the continuum for the helium sequence ions are obtained. Also calculated are the dipole polarizabilities, which are found to be in excellent agreement with the results of other authors.     

The maximum momentum transfer in proton-hydrogen collisions

The upper limit of momentum transfer by a proton to K-shell electrons is calculated in a restricted three-body classical model. The model shows that the infinite upper limit used in practice, is generally good except for low energy protons passing through an extremely rarefied gas.     

Telluro- and seleno-bridged TiIV-MII (M = Ni,Pd, Pt) heterobimetallic complexes

Summary Heterobimetallic complexes of the types [Cp₂Ti(-EAr)₂-M(dppe)] (ClO₄)₂ [(1)–(4); M, E = Ni, Te (1); Ni, Se (2); Pt, Te (3); Pt, Se (4); Ar = Ph (a), C₆H₄-4-Me (b), C₆H₄-4-OMe (c), C₆H₄-4-OEt (d)] and [Cp₂Ti(-TeAr)₂-MCl ₂] [M = Pd (5), Pt (6)] were obtained by the reactions of Cp₂Ti(EAr)₂ with M(dppe)(ClO₄)₂ and M(PhCN)₂Cl₂, respectively. While (1), (5) and (6) are stable in the solid state as well as in solution, (2)–(4) undergo dissociation to M(dppe)(EAr)₂ and Cp₂Ti(ClO₄)₂ in solution, as shown by multinuclear (³¹P{¹H},¹⁹⁵Pt{¹H}, ¹²⁵Te{¹H}) n.m.r. studies. The reaction of Cp₂Ti(SeAr)₂ with M(PhCN)₂Cl₂, however, leads to the formation of Cp₂TiCl₂ and a polymeric material [M(SeAr)₂] _n .     

Spectroscopic correlation for OH stretching frequency shifts of water in crystal hydrates

The shift of the uncoupled OH stretching frequency of water (from its free state position) in crystal hydrates has been plotted against a parameter r⁰ obtained by subtracting the H-bond (OH...Y) length from the sum of the free state ionic radii of O and Y. From an analysis of this curve it is inferred that MO_w coordination in hydrates reduces the ionic size of water oxygen and its effect on the OH stretching frequency is opposite to that of H-bonding.     

Thermal decomposition studies on manganese(III) selenito complexes

The heats of immersion of the systems B₂O₃P₂O₅ and Na₂OB₂O₃P₂O₅ in pyridine have been measured by the use of a solution microcalorimeter. In the composition range R R = atomic ratio, B/P) the heat of immersion was relatively small and was almost independent of R. The heat increased markedly with boron content in R > 1. The increase of heat qualitatively parallels that of surface acidity. Introduction of the Na₂O component reduced both heat of immersion and acidity. MgO was immersed in a benzene solution of benzoic acid. The heat of immersion increased with an increase of surface basicity.     

Siderophore production by a marine Pseudomonas aeruginosa and its antagonistic action against phytopathogenic fungi

A marine isolate of fluorescent Pseudomonas sp. having the ability to produce the pyoverdine type of siderophores under low iron stress (up to 10 μM iron in the succinate medium) was identified as Pseudomonas aeruginosa by using BIOLOG Breathprint and siderotyping. Pyoverdine production was optimum at 0.2% (w/v) succinate, pH 6.0, in an iron-deficient medium. Studies carried out in vitro revealed that purified siderophores and Pseudomonas culture have good antifungal activity against the plant deleterious fungi, namely, Aspergillus niger, Aspergillus flavus, Aspergillus oryzae, Fusarium oxysporum, and Sclerotium rolfsii. Siderophore-based maximum inhibition was observed against A. niger. These in vitro antagonistic actions of marine Pseudomonas against phytopathogens suggest the potential of the organism to serve as a biocontrol agent.     

Intensities of wagging and rocking bands of water in MnCl2 · 2H2O and CoCl2 · 2H2O

IR relative integrated intensities and half-widths of rocking (R) and wagging (W) bands of water in MnCl₂ · 2H₂O and CoCl₂ · 2H₂O are presented at 300 K and 120 K. Departure of observed intensity into D_W/D_R from those predicted by the fixed dipole model is attributed to anisotropic dynamic changes in dipole during these oscillations. A quantity representing the variation of this anisotropy between W and R oscillations is computed and its origin is discussed. An increase by 20% to 50% in both D_W and D_R on lowering the temperature has also been discussed.     

Efficient and environmentally benign synthetic protocol for the synthesis of structurally diverse annulated pyridopyrimidines

Structurally diverse annulated pyridopyrimidines have been synthesized by an efficient and environmentally benign synthetic protocol involving catalyzed four-component reaction of 2-aminobenzothiazoles with thiophene-2-carbaldehyde and carbonyl compounds in ethanol. Mild reaction conditions, operational simplicity, and structural diversity with excellent yields are some special attractions of the present protocol.     

Spectroscopic evidence for the localization of Skyrmions near nu = 1 as T --> 0

Optically pumped nuclear magnetic resonance measurements of 71Ga spectra were carried out in an n-doped GaAs/Al(0.1)Ga0.9As multiple quantum well sample near the integer quantum Hall ground state nu = 1. As the temperature is lowered (down to T approximately 0.3 K), a "tilted plateau" emerges in the Knight shift data, which is a novel experimental signature of quasiparticle localization. The dependence of the spectra on both T and nu suggests that the localization is a collective process. The frozen limit spectra appear to rule out a 2D lattice of conventional Skyrmions.