Two-component Bose-Einstein condensates with a large number of vortices

We consider the condensate wave function of a rapidly rotating two-component Bose gas with an equal number of particles in each component. If the interactions between like and unlike species are very similar (as occurs for two hyperfine states of (87)Rb or (23)Na) we find that the two components contain identical rectangular vortex lattices, where the unit cell has an aspect ratio of sqrt[3], and one lattice is displaced to the center of the unit cell of the other. Our results are based on an exact evaluation of the vortex lattice energy in the large angular momentum (or quantum Hall) regime.     

Chemisorbed halogen adlayers on Fe(110): Electronic band structure and surface geometry

A series of overlayer structures, starting with a c(3 × 1) geometry are formed during the dissociative chemisorption of chlorine, bromine, and iodine on Fe(110). These adlayers provide an opportunity to systematically examine the corresponding changes in electronic band structure as a function of coverage and adsorbate. At coverage levels greater than low-energy electron diffraction patterns obtained from the halogen-covered Fe(110) surface evolve continuously with coverage. The electronic band structure was examined as a function of coverage and adsorbate species via angle-resolved ultraviolet photoelectron spectroscopy. It is concluded that the electronic band structure measurements support an incommensurate structural model for halogen overlayer geometry on Fe(110) in which an overlayer lattice, that is in general incommensurate with the substrate, rotates and compresses with increases in coverage. An alternative interpretation of the diffraction results based on antiphase domain boundaries within the overlayer is not consistent with the photoemission data. The incommensurate model emphasizes adatom-adatom interactions over adatom-substrate interactions while the reverse is true for the antiphase boundary model.     

Search for nucleon resonances of mass up to 8.5 GeV

Missing mass spectra were obtained by measuring recoil protons from the reaction p+p→p+X in the Jacobian peak region. Data were taken during the acceleration ramp of the Fermilab machine using an internal hydrogen gas jet target. We observe the well known N¹(1688) and N¹(2190) resonances but no significant structures at higher mass.     

Theory of electronic structure of non-dilute transition metal alloys : Ni-Cu

The density of states for the Ni-Cu alloy system has been calculated as a function of concentration by the supercell method. This method takes into account inter-site interactions in contrast with current effective medium or single site theories. We show that the method is practical for the study of disordered systems. Comparison is made with previous work as well as with photoemission data.     

Measurement of internuclear distances in solid-state NMR by a background-filtered REDOR experiment

A background-filtered version of the rotational-echo double resonance (REDOR) experiment is demonstrated. The experiment combines a traditional REDOR pulse sequence with a double-cross-polarization (DCP) sequence to select only those signals coming from spin pairs of interest. The relatively inefficient DCP sequence, which transfers polarization from (1)H to (15)N and subsequently to (13)C, is improved by the use of adiabatic passages through the (-1) sideband of the Hartmann-Hahn matching condition. The result is an efficient 2D-REDOR pulse sequence that does not require a reference experiment for removal of background signals. The data produced by the experiment are ideally suited to analysis by newly developed dipolar transform methods, such as the REDOR transform. The relevant features of the experiment are demonstrated on simple labeled amino acids. Relative efficiencies of several other potential filtering methods are also compared. Copyright 2000 Academic Press.     

Synthesis of 5-acetyloxazoles and 1,2-diketones from β-alkoxy-β-ketoenamides and their subsequent transformations

Lithiated alkoxyallenes, nitriles, and carboxylic acids have been employed as precursors in a three-component reaction leading to highly substituted β-alkoxy-β-ketoenamides. Upon treatment with trifluoroacetic acid, these enamides could be easily cyclized to 5-acetyloxazole derivatives. The synthesis is very flexible with respect to the substitution pattern at C-2 and C-4 of the oxazole core. A mechanistic suggestion for the oxazole formation is presented on the basis of (18)O-labeled compounds and their mass spectrometric analysis. In several cases, 1,2-diketones are formed as side products or even as major components. The acetyl moiety at C-5 of the oxazole derivatives can efficiently be converted into alkenyl or alkynyl moieties, which allows a multitude of subsequent reactions. Condensation reactions of the acetyl group provided the expected oxime or hydrazone. By applying a Fischer reaction, the phenylhydrazone could be transferred into an indole, which emphasizes the potential of 5-acetyloxazoles for the preparation of highly substituted (poly)heterocyclic systems. The alkynyl group at C-2 is prone to addition reactions, providing an enamine with interesting photophysical properties. Sonogashira couplings were performed with 5-alkynyl-substituted oxazoles, furnishing the expected aryl-substituted products. This alkynyl unit was employed for the preparation of a new, star-shaped trisoxazole derivative. The ability of this multivalent compound to form self-assembled monolayers between the basal plane of highly oriented pyrolytic graphite and 1-phenyloctane was demonstrated by scanning tunneling microscopy (STM). The star-shaped compound seems to prefer the C(3)-symmetric arrangement in this two-dimensional crystal. Two 1,2-diketones were smoothly converted into functionalized quinoxaline derivatives.