Side-Chain Liquid-Crystalline Polymers with Polystyrene Backbone

Abstract

A series of liquid-crystalline polystyrene derivatives with pendant mesogenic groups has been prepared and characterized. The side-chain is connected to the polystyrene backbone by a methyleneoxyhexyloxy spacer. The mesogenic group is a 4-alkoxy substituted biphenyl group. The length of the alkoxy end-group varied from a methoxy group to an octyloxy group. The polymers were synthesized by a radical reaction. Molar masses (M _n) varied between 17,000 and 46,000, with a molar mass distribution between 1.6 and 2.0. All the polymers were liquid-crystalline, with enantiotropic smectic phases. The polymers were characterized with polarizing microscopy, NMR spectroscopy, and calorimetry.     

Succinobucol's new coat--conjugation with steroids to alter its drug effect and bioavailability

Synthesis, detailed structural characterization (X-ray, NMR, MS, IR, elemental analysis), and studies of toxicity, antioxidant activity and bioavailability of unique potent anti-atherosclerotic succinobucol-steroid conjugates are reported. The conjugates consist of, on one side, the therapeutically important drug succinobucol ([4-{2,6-di-tert-butyl-4-[(1-{[3-tert-butyl-4-hydroxy-5-(propan-2-yl)phenyl]sulfanyl}ethyl)sulfanyl]phenoxy}-4-oxo-butanoic acid]) possessing an antioxidant and anti-inflammatory activity, and on the other side, plant stanol/sterols (stigmastanol, β-sitosterol and stigmasterol) possessing an ability to lower the blood cholesterol level. A cholesterol-succinobucol prodrug was also prepared in order to enhance the absorption of succinobucol through the intestinal membrane into the organism and to target the drug into the place of lipid metabolism-The enterohepatic circulation system. Their low toxicity towards mice fibroblasts at maximal concentrations, their antioxidant activity, comparable or even higher than that of ascorbic acid as determined by direct quenching of the DPPH radical, and their potential for significantly altering total and LDL cholesterol levels, suggest that these conjugates merit further studies in the treatment of cardiovascular or other related diseases. A brief discussion of succinobucol's ability to quench the radicals, supported with a computational model of the electrostatic potential mapped on the electron density surface of the drug, is also presented.     

Microscopic calculations of isospin-breaking corrections to superallowed beta decay

The superallowed β-decay rates that provide stringent constraints on physics beyond the standard model of particle physics are affected by nuclear structure effects through isospin-breaking corrections. The self-consistent isospin- and angular-momentum-projected nuclear density functional theory is used for the first time to compute those corrections for a number of Fermi transitions in nuclei from A=10 to A=74. The resulting leading element of the Cabibbo-Kobayashi-Maskawa matrix, |V(ud)|=0.97447(23), agrees well with the recent result of Towner and Hardy [Phys. Rev. C 77, 025501 (2008)].     

Hydrolysis of Phosphodiester Bonds within RNA Hairpin Loops in Buffer Solutions: the Effect of Secondary Structure on the Inherent Reactivity of RNA Phosphodiester Bonds

The hydrolysis of phosphodiester bonds of chimeric 2′-O-methyloligoribonucleotides was studied in buffer solutions. Pseudo-first-order rate constants for cleavage of phosphodiester bonds within hairpin loops were calculated and compared with those for cleavage of phosphodiester bonds within double-stranded stems and linear single-stranded oligonucleotides. No large differences in reactivity were observed: some of the hairpin structures studied were slightly less and others slightly more reactive than the linear reference. These results suggest that phosphodiester bonds within small hairpin loops are conformationally free to cleave by an in-line mechanism, but also that the secondary structure may influence the reactivity of phosphodiester bonds.     

Suppressor current switching: a simple and effective means to reduce background noise in ion chromatography

Background noise in ion chromatography with suppressed conductivity detection was significantly reduced for the period of time when the electric current to an anion self regenerating suppressor (ASRS) running in the recycle mode was turned-off. With high capacity AS11-HC columns, it was possible to maintain current free conditions from the beginning of the run past the chloride peak, which enables routine high sensitivity analysis of early to mid eluting peaks. This suppressor current switching was utilized for the analysis of bromate in drinking water with large volume injection using on-line removal of chloride by an On-Guard Ag+-cartridge. The method detection limit (MDL) was 0.21 microg/l in fortified reagent water. Coelution of bromate with an unknown compound was observed, but it was solved by the optimization of gradient program.     

Synthesis of (-)-matairesinol, (-)-enterolactone,and (-)-enterodiol from the natural lignan hydroxymatairesinol

[reaction: see text] We describe here a four-step semisynthetic method for the preparation of enantiomerically pure (-)-enterolactone starting from the readily available lignan hydroxymatairesinol from Norway spruce (Picea abies). Hydroxymatairesinol was first hydrogenated to matairesinol. Matairesinol was esterified to afford the matairesinyl 4,4'-bistriflate, which was deoxygenated by palladium-catalyzed reduction to 3,3'-dimethylenterolactone. Demethylation of 3,3'-dimethylenterolactone and reduction with LiAlH(4) yielded (-)-enterolactone and (-)-enterodiol, respectively.     

The method of invariants applied to the analysis of 57Fe Mössbauer spectra

The performance of proposed antihydrogen spectroscopy or gravity experiments will crucially depend on the temperature of the initial antihydrogen sample. Measurements by ATRAP and ATHENA have shown that antihydrogen produced with the nested-trap technique is much hotter than the temperature of the surrounding trap. Therefore, novel schemes for antihydrogen recombination as well as for the pre-cooling of antiprotons are being considered. We are investigating a possible antiproton cooling technique based on the laser cooling of negative osmium ions. If demonstrated to be successful, it will allow the sympathetic cooling of antiprotons—or any negatively charged particles—to microkelvin temperatures. As a first milestone toward the laser cooling of negative ions, we have performed collinear laser spectroscopy on negative osmium and determined the transition frequency and the cross-section of the relevant bound–bound electric-dipole transition.