The systematics of hyperfine magnetic fields at sp impurities on the Z-sites in Co based Heusler alloys are investigated. New TDPAC measurements of Cd hyperfine fields are reported. 相似文献
Hydrophobic interactions control the morphologies of both surfactant aggregates and proteins. Globular proteins "denature" upon addition of excess amounts of denaturants such as urea. Understanding the microscopic basis of the urea effect on proteins or supramolecular aggregates such as micelles has always been a debated issue. Inspired by this need, the effect of urea (U), thiourea (TU), monomethylurea (MMU), dimethylurea(DMU), tetramethylurea (TMU), dimethylthiourea (DMTU), and tetramethylthiourea (TMTU) on the structural transition (spherical micelles to rod-shaped micelles, s --> r) in the sodium dodecylbenzenesulfonate (SDBS)-1-pentanol system has been investigated through dynamic light scattering(DLS) and viscosity measurements at 25 degrees C. 1-Pentanol, at 0.14 M, is found to promote s --> r in this system (0.2 M SDBS). The presence of the additives causes, in almost all cases, a decrease and increase in this 1-pentanol concentration depending upon the concentration and nature of the additive. These effects are explained in terms of an increased dielectric constant of the solvent medium due to the presence of additives and increased micellar hydration due to the repulsion of charged monomers caused by adsorption of the additives. Taken together, the data signal the exposure of biological assemblies to water at higher [additive], which causes a decrease in hydrophobic interactions responsible for compact structure formation (i.e., native protein). 相似文献
Metabolic activation of drug candidates to electrophilic reactive metabolites that can covalently modify cellular macromolecules may result in acute and/or idiosyncratic immune system-mediated toxicities in humans. This presents a significant potential liability for the future development of these compounds as safe therapeutic agents. We present here an example of an approach where sites of metabolic activation within a new drug candidate series were rapidly identified using online liquid chromatography/multi-stage mass spectrometry on an ion trap mass spectrometer. This was accomplished by trapping the reactive intermediates formed upon incubation of compounds with rat and human liver microsomes as their corresponding glutathione conjugates and mass spectral characterization of these thiol adducts. Based on the structures of the GSH adducts identified, potential sites and mechanisms of bioactivation within the chemical structure were proposed. These metabolism studies were interfaced with iterative structural modifications of the chemical series in order to block these bioactivation sites within the molecule. This strategy led to a significant reduction in the propensity of the compounds to undergo metabolic activation as evidenced by reductions in the irreversible binding of radioactivity to liver microsomal material upon incubation of tritium-labeled compounds with this in vitro system. With the efficiency and throughput achievable with such an approach, it appears feasible to identify and address the metabolic activation potential of new drug leads during routine metabolite identification studies in an early drug discovery setting. 相似文献
Summary The iron(III) compound, FeCl(OH)(MeCO2) · MeCO2H · 0.5 H2O, (1), interacts with the sample bidentate ligand, 2,2-bipyridyl (bipy), to form an aduct, Fe2Cl2(OH)2(MeCO2)2 · (bipy). By the loss of protons, anthranilic (anthH) and salicylic (salH2) acids behave as uninegative charged ligands to give FeCl(anth)2 · H2O and FcCl(salH)2 · H2O, respectively. The former decomposes on heatingin vacuo to form Fe2O(anth)4 while the latter yields Fe2O(sal)2. Acetylacetone (acacH) and 8-hydroxyquinoline (quinH) give FeCl(acac)2 and FeCl(quin)2 · (quinH). The latter desolvates at 140°/10–4 torr to form FeCl(quin)2. l.r. spectra, thermal decomposition, molar conductance and magnetic susceptibility studies at room temperature have been used to characterize these compounds. 相似文献
Trimethylsilyldiethylamine Me3SiNEt2 and MoOCl4 (1:1) undergo a free radical redox reaction in CH2Cl2 or Et2O to form MoCl3O(HNEt2). Reduction occurs even in aprotic media like CCl4 and CS2 to give MoV complexes Mo2Cl6O2(N2Et4) and Mo2Cl6O2[(SCNEt2)2S2], respectively. A 2:1 reaction in nonionizing protic solvents undergoes redox cum cleavage to provide MoCl2O(NEt2) (HNEt2) but a reaction at reflux temperature in 1,2-dichloroethane leads to diethylammonium salt, [Et2NH2][MoCl4O(HNEt2)]. Higher molar reactions (3:1, 4:1) in CH2Cl2 or Et2O are associated with redox reaction as well as oxygen atom abstraction to form de-oxo MoIV complex MoCl3(NEt2)(HNEt2)2, whereas, a 3:1 reaction in CS2 forms Mo2Cl4O(S2CNEt2)4. Compounds have been characterized by elemental analyses, redox titration, magnetic moment, conductance, infrared, electronic absorption and 1H-NMR measurements. 相似文献
JPC – Journal of Planar Chromatography – Modern TLC - A water-in-oil microemulsion has been used for the first time as a mobile phase in thin-layer chromatography of amino acids. A new... 相似文献
Copper(II) tetrafluoroborate has been found to be a new and highly efficient catalyst for Michael addition of thiols to α,β-unsaturated carbonyl compounds under solvent-free conditions and in H2O at room temperature. The reactions are very fast and are completed in 2 min to 1 h affording high yields. The rate of thiol addition was dependent on the steric hindrance at the β-carbon of the α,β-unsaturated carbonyl substrate. In the case of chalcones, the reactions are best carried out in MeOH as solvent. 相似文献
The Ramanujan Journal - This paper provides elementary proofs for several types of congruences involving multipartitions and self-convolutions of the divisor function. Our computations use... 相似文献
Summary The binuclear iron(III) compound, Fe2Cl(OH)2(MeCO2)3 2 AcOH combines with pyridine, -picoline and 2,2-bipyridyl (B) to form Fe2Cl(OH)2(AcO)3·B adducts. The secondary bases, pyrrolidine and diethylamine (RNH), on the other hand, combine with the complete elimination of chlorine to form, Fe2(NR)(OH)2(AcO)3. These products have been characterised by molecular weight, i.r. spectra, magnetic susceptibility and Mössbauer measurements. 相似文献
Life-threatening diseases, especially those caused by pathogens and harmful ultraviolet radiation (UV-R), have triggered increasing demands for comfortable, antimicrobial, and UV-R protective clothing with a long service life. However, developing such textiles with exceptional wash durability is still challenging. Herein, we demonstrate how to fabricate wash durable multifunctional cotton textiles by growing in situ ZnO-TiO2 hybrid nanocrystals (NCs) on the surface of cellulosic fabrics. The ZnO-TiO2 hybrid NCs presented high functional efficiency, owing to their high charge transfer/separation. Ultrafine fiber surface pores, utilized as nucleating sites, endowed the uniform growth of NCs and their physical locking. The resulting fabrics presented excellent UV protection factors up to 54, displayed bactericidal efficiency of 100% against Staphylococcus aureus and Escherichia coli, and optimum self-cleaning efficacy. Moreover, the functionalized textiles exhibited robust washing durability, maintaining antibacterial and anti-UV-R efficiency even after 30 extensive washing cycles.