Magnetoelectronic transport of the two-dimensional electron gas in CdSe single quantum wells

Hall mobility and magnetoresistance coefficient for the two-dimensional (2D) electron transport parallel to the heterojunction interfaces in a single quantum well of CdSe are calculated with a numerical iterative technique in the framework of Fermi-Dirac statistics. Lattice scatterings due to polar-mode longitudinal optic (LO) phonons, and acoustic phonons via deformation potential and piezoelectric couplings, are considered together with background and remote ionized impurity interactions. The parallel mode of piezoelectric scattering is found to contribute more than the perpendicular mode. We observe that the Hall mobility decreases with increasing temperature but increases with increasing channel width. The magnetoresistance coefficient is found to decrease with increasing temperature and increase with increasing magnetic field in the classical region.      

Dioxovanadium(V) Complexes Incorporating Tridentate ONO Donor Hydrazone Ligands Derived from Acetylhydrazide and 2-hydroxybenzaldehyde/2-hydroxyacetophenone. Synthesis, Characterization and Reactivity

Reaction of VOSO₄ with the tridentate ONO donor ligand derived from the condensation of acetylhydrazide with either 2-hydroxybenzaldehyde (H₂L¹) or 2-hydroxyacetophenone (H₂L²) (general abbreviation H₂L) in an equimolar ratio in the presence of two equivalents of sodium acetate in aqueous-methanolic medium in air produces yellow dioxovanadium(V) complexes of the type, [V^vO₂(H⁺-L)], (1) and (2) in good yield. Aerial oxygen is most likely the oxidant (for the oxidation of V^IV→V^V) assisted by the ligand basicity. Complexes are characterized by elemental analyses and by i.r., n.m.r. and u.v.–vis. spectroscopies. I.r. spectra of the complexes indicate the tridentate dinegative forms of the ligands. The ¹H-n.m.r. spectrum of (2) in CD₃CN solvent indicates the presence of a strongly deshielded N–H proton. Conductivity measurements in DMF solution indicate that the complexes are non-electrolytic and so the H⁺ ion is strongly bonded probably with the uncoordinated imine-N nitrogen of the coordinated Schiff base moiety. Both complexes exhibit only the LMCT band in the u.v. region in MeOH and they are electroactive, displaying an irreversible reduction peak near −0.35 V versus s.c.e. in methanol solution. Methanol solutions of the complexes are reversibly reduced by ascorbic acid to the corresponding V^IV analogue as is evident from their u.v.–vis. spectra. The CH₂Cl₂ suspension of these complexes (1) and (2) reacts separately with 8-hydroxyquinoline (Hhq) in air to produce the mixed-ligand complexes of the type [V^vO(L)(hq)].     

A linear time algorithm to remove winding of a simple polygon

In this paper, we present a linear time algorithm to remove winding of a simple polygon P with respect to a given point q inside P. The algorithm removes winding by locating a subset of Jordan sequence that is in the proper order and uses only one stack.     

QCD phase transition in rotating neutron star,neutrino beaming and gamma-ray bursters

We have studied the emission of neutrinos from a rotating hybrid star. We find that the emission is predominantly confined to a very small angle, provided the core of the star is in a mixed phase of quarks and hadrons and the size of such a mixed phase is small. Annihilation of neutrinos to produce gamma rays has been discussed. The estimated duration of the burst is found to be within the observational range.     

Visual sensing of fluoride ions by dipyrrolyl derivatives bearing electron-withdrawing groups

Two new, easy-to-prepare dipyrrolyl derivatives endowed with electron-withdrawing quinone or dicyano functionalities in their architecture permit the detection of fluoride ions under visual (naked-eye) as well as optical (absorption and fluorescence) and electrochemical conditions in organic solvents     

Theorie. Methode

Ohne Zusammenfassung     

Exotic cosmic family events. Aspects of observations and theories

Summary Against the background of the experimental reports obtained so far some very recent theoretical approaches to the understanding of the exotic family events in cosmic-ray physics have been traced in a comprehensive manner. The main trends in the observations have been highlighted and the limitations of the theoretical attempts have been pointed out.     

A comparative study of Gaussian geostatistical models and Gaussian Markov random field models

Gaussian geostatistical models (GGMs) and Gaussian Markov random fields (GMRFs) are two distinct approaches commonly used in spatial models for modeling point-referenced and areal data, respectively. In this paper, the relations between GGMs and GMRFs are explored based on approximations of GMRFs by GGMs, and approximations of GGMs by GMRFs. Two new metrics of approximation are proposed : (i) the Kullback-Leibler discrepancy of spectral densities and (ii) the chi-squared distance between spectral densities. The distances between the spectral density functions of GGMs and GMRFs measured by these metrics are minimized to obtain the approximations of GGMs and GMRFs. The proposed methodologies are validated through several empirical studies. We compare the performance of our approach to other methods based on covariance functions, in terms of the average mean squared prediction error and also the computational time. A spatial analysis of a dataset on PM_2.5 collected in California is presented to illustrate the proposed method.     

Kinetic study of the reactions of p‐nitrophenyl acetate and p‐nitrophenyl benzoate with oximate nucleophiles

The reactions of p‐nitrophenyl acetate (PNPA) and p‐nitrophenyl benzoate (PNPB) with α‐nucleophile oximates, that is, butane 2,3‐dione monoximate, pralidoximate, and other oximates have been studied in the presence of different cationic surfactants. The first‐order rate constant increases with increasing surfactant concentration. The extent of acceleration is dependent on the head group structure of surfactants. The PNPA is more reactive than PNPB toward all the nucleophiles at higher concentration of surfactants. © 2008 Wiley Periodicals, Inc. Int J Chem Kinet 41: 57–64, 2009