Iterative solutions for low lying excited states of a class of SchrSdinger equation

The convergent iterative procedure for solving the groundstate Schr?dinger equation is extended to derive the excitation energy and the wavefunction of the low-lying excited states. The method is applied to the one-dimensional quartic potential problem. The results show that the iterative solution converges rapidly when the coupling g is not too small.     

Reactivity of γ-chloro-gem-trichloroalkanes with chromous chloride

CrCl₂-mediated condensation of γ-chloro-gem-trichloroalkanes with aldehyde generates homoallylic alcohols through a hydride rearrangement followed by a Nozaki-Hiyama allylation.     

The epitaxial sexiphenyl (0 0 1) monolayer on TiO2(1 1 0): A grazing incidence X-ray diffraction study

A para-sexiphenyl monolayer of near up-right standing molecules (nominal thickness of 30 Å) is investigated in-situ by X-ray diffraction using synchrotron radiation and ex-situ by atomic force microscopy. A terrace like morphology is observed, the step height between the terraces is approximately one molecular length. The monolayer terraces, larger than 20 μm in size, are extended along the [0 0 1] direction of the TiO₂(1 1 0) substrate i.e. along the Ti-O rows of the reconstructed substrate surface. The structure of the monolayer and its epitaxial relationship to the substrate is determined by grazing incidence X-ray diffraction. Extremely sharp diffraction peaks reveal high crystalline order within the monolayer, which was found to have the bulk structure of sexiphenyl. The monolayer terraces are epitaxially oriented with the (0 0 1) plane parallel to the substrate surface (out-of-plane order). Four epitaxial relationships are observed. This in-plane alignment is determined by the arrangement of the terminal phenyl rings of the sexiphenyl molecules parallel to the oxygen rows of the substrate.     

Probing antiferromagnetic order with heat capacity in exchange-biased structures

We explore the magnetic heat capacity in exchange-biased ferromagnet/antiferromagnet bilayers theoretically. We show that changes in the antiferromagnetic structure due to the reversal of the ferromagnet layer can be detected by distinct features in the heat capacity. This offers a method for probing antiferromagnetic domains in exchange-biased systems.     

Baer orderings with noninvariant valuation ring

We construct division algebras with involution containing a Baer ordering with noninvariant order ring. This gives a negative answer to a question of Holland, whether the order ring is always invariant under inner automorphisms. Furthermore, we give examples of any index. Previously, the only known examples of division algebras containing Baer orderings were of index 2 ⁿ or of indexp forp a prime of the form 4m + 3. Supported in part by the National Science Foundation.     

Neutron emission under particular nonequilibrium conditions from Pd and Ti electrolytically charged with deuterium

Summary We report on neutron emission in palladium and titanium electrolitically charged with deuterium. The detection of neutrons is observed after thermal treatment of the electrode. In the hypothesis that neutrons came from cold fusion processes, we estimate a fusion rate as high as 1.3·10⁻²¹ fusions/deuteron pair/second.     

Superfield equations forN=1 massive multiplets

We consider equations of motion for some massiveN=1 supermultiplets of fields, using superfields and their superderivatives. The formalism is based on the superprojectors.     

Electrochemical Fluorosulfation of Fluoroalkenes: Factors Determining the Process Selectivity

A comparison of results of indirect and direct electrochemical fluorosulfation of nonsaturated fluorocarbons shows that the main or the only product in potentiostatic conditions is vicinal fluorosulfates. Owing to a high rate of the electrochemical step, which exceeds the rate of desorption of intermediate radicals from the electrode surface into solution, it is possible to improve the process selectivity by increasing the contribution of the ionic reaction route.     

Interaction of metals with an organic semiconductor: Ag and In on PTCDA

The interaction of Ag and In with a thin film of 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA) was studied by near-edge X-ray absorption fine structure (NEXAFS). Upon Ag deposition on a PTCDA film of 20 nm thickness the relative intensities and lineshapes, as well as the angular dependence of the spectra remains unchanged, illustrating the formation of a chemically unreactive Ag/PTCDA interface. On the other hand, the adsorption of 0.3 nm In strongly decreases the intensity of the π^* resonances in C and O K-edge NEXAFS spectra. This is attributed to a strong charge transfer between In and PTCDA, leading to a redistribution of the charge in the molecule. However, the absence of a strong shift or new features and negligible dependence of peak intensities corresponding to π^* resonances on the In thickness indicate that the interaction between In and PTCDA is not accompanied by a covalent bond formation.