Crystallized vortex crystals

Numerical simulations of the equations of motion of 300 charged particles confined to a plane with an additional magnetic field orthogonal to the plane reproduce recently observed self-organization of non-neutral plasmas into a small number of interacting vortices. In the presence of damping we observe crystallized vortices, i.e. vortices with regular internal structure. We also observe crystallized vortex crystals, i.e. geometric patterns of crystallized vortices. Fractal vortex arrangements are investigated and found to be stable. Our results are relevant for quantum dots and artificial atoms. Received: 24 February 1998 / Revised: 4 March 1998 / Accepted: 4 May 1998     

Über galvinole und galvinoxyl-mehrspinsysteme—I : Eine neue metallorganische synthese von mono- und oligo-galvinolen

The synthesis of the so far unknown organometallic compound (2,6 - di - tert. - butyl - 4 - lithiumphenoxy) - trimethylsilane is most useful for the general introduction of the 3,5 - di - tert. - butyl - 4 - hydroxyphenyl group. Using the esters of aromatic mono-, di-, and tricarboxylic acids mono-, bis-, and tris-galvinoles are obtainable, while nitriles and dimethyl formamide are converted into ketones and the 3,5 - di - tert. - butyl - 4 - hydroxybenzaldehyde, respectively. In the present paper the experimental procedure and structure determination of the compounds in question are described.     

Threshold Photoelectron Spectroscopy of IO and HOI

Iodine oxides appear as reactive intermediates in atmospheric chemistry. Here, we investigate IO and HOI by mass-selective threshold photoelectron spectroscopy (ms-TPES), using synchrotron radiation. IO and HOI are generated by photolyzing iodine in the presence of ozone. For both molecules, accurate ionization energies are determined, 9.71±0.02 eV for IO and 9.79±0.02 eV for HOI. The strong spin-spin interaction in the ³Σ⁻ ground state of IO⁺ leads to an energy splitting into the Ω=0 and Ω=±1 sublevels. Upon ionization, the I−O bond shortens significantly in both molecules; thus, a vibrational progression, assigned to the I−O stretch, is apparent in both spectra.     

Short monolithic beds: history and introduction to the field

The history of the development of short monolithic beds is described.     

Assignment of carbon chain molecules in cryogenic matrices by selective laser-induced oxidation

We tested and applied a laser-induced oxidation method for identifying the IR-active stretching mode absorptions of linear C(2)(n)(+1) molecules which have known strong UV-vis absorptions. For this purpose, we trapped the molecules of carbon vapor in non-inert matrices (pure O(2) and Ar-O(2) mixtures) at temperatures providing molecular growth. The matrix was exposed to laser light tuned to the wavelength of the UV-vis transition of a specific carbon species. We observed a bleaching of that UV-vis absorption and a correlated decrease of lines in the IR spectra for C(9), C(11), C(13), C(15), and C(21). The data suggest that the strongest IR absorptions of the C(2)(n)(+1) (n > or = 4) chains form a regular pattern with increasing n. To obtain information about IR absorptions of carbon chain oxides, oxygen matrices with replaced (16)O --> ( 18)O isotopes were applied. Our data revise some of the IR assignments existing in the literature.     

Kinetic control in the acid-catalyzed isomerization of trans-2-,vinyl-1,6-dimethylbicyclo[4.3.O]non-2-en-7-one

The acid-catalyzed isomerization of the title compound (2) to the thermodynamically-favored Z isomer 4 proceeds first to the E-isomer 3.     

The synthesis of bicyclo[2.2.2]octan-2-ones by sequential michael reactions

The reaction of cross-conjugated dienolate anions derived from substituted cyclohexenones with methyl acrylate and vinyl ketones has been studied. Bicyclo[2.2.2]octan-2-ones are formed by a sequential Michael mechanism; however, the reactions of vinyl ketones must be conducted under amine-free conditions. Unexpecedly, the conjugate base from 2,3-dimethylcyclohex-2-enone gives only a single Michael adduct with vinyl ketones, and if forced to react further undergoes an intramolecular aldol condensation. An alternative Diels-Alder approach to the bicyclo[2.2.2]octanone products is shown to be effective.     

High-performance membrane chromatography of serum and plasma membrane proteins.

Porous discs made of poly(glycidyl methacrylate) were used for high-performance membrane chromatography (HPMC) of proteins. In model experiments, separations of standard proteins by anion-exchange HPMC using a DEAE disc were carried out. The influences of sample distribution and disc diameter and thickness on separation performance were studied. The separation disc allowed a scaling-up from analytical (diameter 10 mm) to semi-preparative (diameter 50 mm) dimensions. In an application study, separations with anion-exchange and affinity HPMC were carried out using different complex samples such as rat serum and plasma membrane proteins. In all experiments the results on poly(glycidyl methacrylate) discs were comparable to those achieved on adequate high-performance liquid chromatographic (HPLC) columns. However, the separations on HPMC discs could be carried out faster than corresponding separations on HPLC columns. The pressure drop on the discs was low even at high flow-rates. The experiments show that the poly(glycidyl methacrylate) discs used are especially suitable for the isolation of proteins and other biopolymers which occur in a diluted state in complex mixtures.