On the nature of the magnetoplastic effect in a beryllium condensate

The effect of a weak constant magnetic field on the temperature and amplitude dependences of the effective shear modulus, low-frequency internal friction, and the ratio of velocities of the dislocation motion in a magnetic field and without it in a beryllium condensate has been investigated. It has been shown that the simultaneous action of a constant magnetic field, mechanical stresses, and a variable temperature results in sign reversal of the magnetoplastic effect in beryllium. It has been found that the sign reversal of the magnetoplastic effect is accompanied by the sign reversal of the ratio of velocities of the dislocation motion, as well as by oscillations in the temperature dependence of this ratio. Possible mechanisms of manifestation of the magnetoplastic effect in beryllium have been discussed in terms of the results of the comprehensive analysis of the amplitude dependences of the studied characteristics.     

What can we learn from N2O isotope data? – Analytics,processes and modelling

The isotopic composition of nitrous oxide (N₂O) provides useful information for evaluating N₂O sources and budgets. Due to the co-occurrence of multiple N₂O transformation pathways, it is, however, challenging to use isotopic information to quantify the contribution of distinct processes across variable spatiotemporal scales. Here, we present an overview of recent progress in N₂O isotopic studies and provide suggestions for future research, mainly focusing on: analytical techniques; production and consumption processes; and interpretation and modelling approaches. Comparing isotope-ratio mass spectrometry (IRMS) with laser absorption spectroscopy (LAS), we conclude that IRMS is a precise technique for laboratory analysis of N₂O isotopes, while LAS is more suitable for in situ/inline studies and offers advantages for site-specific analyses. When reviewing the link between the N₂O isotopic composition and underlying mechanisms/processes, we find that, at the molecular scale, the specific enzymes and mechanisms involved determine isotopic fractionation effects. In contrast, at plot-to-global scales, mixing of N₂O derived from different processes and their isotopic variability must be considered. We also find that dual isotope plots are effective for semi-quantitative attribution of co-occurring N₂O production and reduction processes. More recently, process-based N₂O isotopic models have been developed for natural abundance and ¹⁵N-tracing studies, and have been shown to be effective, particularly for data with adequate temporal resolution. Despite the significant progress made over the last decade, there is still great need and potential for future work, including development of analytical techniques, reference materials and inter-laboratory comparisons, further exploration of N₂O formation and destruction mechanisms, more observations across scales, and design and validation of interpretation and modelling approaches. Synthesizing all these efforts, we are confident that the N₂O isotope community will continue to advance our understanding of N₂O transformation processes in all spheres of the Earth, and in turn to gain improved constraints on regional and global budgets.     

Christensen measurable solutions of some functional equation

Let X be a separable F-space over the field K of reals or complex numbers. We characterize solutions of the equation

f(x+M(f(x))y)=f(x)f(y)     

Effective Use of Empirical Data for Virtual Screening against APJR GPCR Receptor

Alzheimer’s disease is a neurodegenerative disorder incompatible with normal daily activity, affecting one in nine people. One of its potential targets is the apelin receptor (APJR), a G-protein coupled receptor, which presents considerably high expression levels in the central nervous system. In silico studies of APJR drug-like molecule binding are in small numbers while high throughput screenings (HTS) are already sufficiently many to devise efficient drug design strategies. This presents itself as an opportunity to optimize different steps in future large scale virtual screening endeavours. Here, we ran a first stage docking simulation against a library of 95 known binders and 3829 generated decoys in an effort to improve the rescoring stage. We then analyzed receptor binding site structure and ligands binding poses to describe their interactions. As a result, we devised a simple and straightforward virtual screening Stage II filtering score based on search space extension followed by a geometric estimation of the ligand—binding site fitness. Having this score, we used an ensemble of receptors generated by Hamiltonian Monte Carlo simulation and reported the results. The improvements shown herein prove that our ensemble docking protocol is suited for APJR and can be easily extrapolated to other GPCRs.     

Polarographische Gehaltsbestimmung des Chlordiazepoxids (Librium®) in seinen Arzneiformen

Chlorodiazepoxide (I), in its ten different commercial formulations, can be assayed by dc-polarography very rapidly with a relative standard deviation of 2%, without the need for initial separation from other drugs or excipients. This method provides a distinct improvement over most u.v. spectroscopic methods. In addition, differential pulse polarography is a very useful and sensitive method for determination of I in single dóse preparations.     

Polarographische Gehaltsbestimmung des Chlordiazepoxids (Librium?) in seinen Arzneiformen

Zusammenfassung Chlordiazepoxid (I) läßt sich in seinen 10 verschiedenen handelsüblichen Arzneiformen ohne Abtrennung weiterer Wirkstoffe bzw. galenischer Hilfsstoffe gleichspannungspolarographisch mit relativen Standardabweichungen um 2% rasch bestimmen. Zum Vergleich mit Hilfe der Spektralphotometrie erarbeitete Resultate sind z.T. deutlich schlechter. Vorzüglich eignet sich auch die differentielle Pulspolarographie zur I-Bestimmung in einzelnen Dragees, Kapseln usw.Wir danken dem Fonds der Chemischen Industrie, Frankfurt a. M., für finanzielle Unterstützung und Herrn O. Schreiber für stets umsichtige Mitarbeit. F. I. Sengün dankt der Alexander von Humboldt-Stiftung für ein zweijähriges Forschungsstipendium.     

Synthesis of Fluorescent Naphthoquinolizines via Intramolecular Houben–Hoesch Reaction

The repertoire of synthetic methods leading to aza‐analogues of polycyclic aromatic heterocycles has been enlarged by the discovery of the rearrangement of 10‐substituted benzo[h]quinolines into compounds bearing an azonia‐pyrene moiety. Acid‐mediated intramolecular cyclization of derivatives bearing ‐CH₂CN and ‐CH₂CO₂Et groups led to compounds bearing a 5‐substituted benzo[de]pyrido[3,2,1‐ij]quinolinium core. Advanced photophysical studies including time‐correlated single photon counting (TCSPC) and transient absorption spectroscopy of 5‐aminobenzo[de]pyrido[3,2,1‐ij]quinolin‐4‐ium salt and 5H‐benzo[de]pyrido[3,2,1‐ij]quinolin‐5‐one showed their promising optical properties such as high fluorescence quantum yields (37–59 %), which was almost independent of the solvent, and high tenability of the absorption band position upon changing the solvent. The benzo[de]pyrido[3,2,1‐ij]quinolinium salt selectively stains nucleic acids (in the nucleus and mitochondria) in eukaryotic cells.     

Hydrogen bonding mediated by key orbital interactions determines hydration enthalpy differences of phosphate water clusters

Electronic structure calculations have been carried out to provide a molecular interpretation for dihydrogen phosphate stability in water relative to that of metaphosphate. Specifically, hydration enthalpies of biologically important metaphosphate and dihydrogen phosphate with one to three waters have been computed with second-order M?ller-Plesset perturbation and density functional theory (B3LYP) with up to the aug-cc-pvtz basis set and compared to experiment. The inclusion of basis set superposition error corrections and supplemental diffuse functions are necessary to predict hydration enthalpies within experimental uncertainty. Natural bond orbital analysis is used to rationalize underlying hydrogen bond configurations and key orbital interactions responsible for the experimentally reported difference in hydration enthalpies between metaphosphate and dihydrogen phosphate. In general, dihydrogen phosphate forms stronger hydrogen bonds compared to metaphosphate due to a greater charge transfer or enhanced orbital overlap between the phosphoryl oxygen lone pairs, n(O), and the antibonding O-H bond of water. Intramolecular distal lone pair repulsion with the donor n(O) orbital of dihydrogen phosphate distorts symmetric conformations, which improves n(O) and sigma*(O-H) overlap and ultimately the hydrogen bond strength. Unlike metaphosphate, water complexed to dihydrogen phosphate can serve as both a hydrogen bond donor and a hydrogen bond acceptor, which results in cooperative charge transfer and a reduction of the energy gap between n(O) and sigma*(O-H), leading to stronger hydrogen bonds. This study offers insight into how orbital interactions mediate hydrogen bond strengths with potential implications on the understanding of the kinetics and mechanism in enzymatic phosphoryl transfer reactions.     

Chemical Composition,Antioxidant and Antimicrobial Activity of Some Types of Honey from Banat Region,Romania

Honey is a natural product with multiple health benefits. The paper presents the chemical characterization and the antioxidant and antimicrobial potential of ten types of honey (knotweed, linden, wild cherry, acacia, honeydew, oilseed rape, sunflower, phacelia, plain polyflora and hill polyflora) from the Banat region, Romania. We studied the water content, dry matter, impurities, acidity and pH of honey. We also determined the content of reducing sugar, minerals and flavonoids and the total phenolic content. All honey samples analysed showed good nutritional characteristics according to the standard codex for honey. From the analysis of the mineral content of the honey samples, we observed a variability in the macro and microminerals, influenced by the botanical origin, ranging between 0.25% (wild cherry honey) and 0.54% (honeydew). The toxic metals’ (Cd and Pb) levels met the standard for almost all samples analysed except for knotweed. The flavonoid content of the samples ranged from 9.29 mg QE/100 g for wild cherry honey to 263.86 mg QE/100 g for linden honey, and for polyphenols between 177.6 mgGAE/100 g for acacia honey and 1159.3 mgGAE/100 g for honeydew. The best antioxidant capacity was registered in the case of linden honey (79.89%) and honeydew (79.20%) and the weakest in acacia (41.88%) and wild cherries (50.4%). All studied honey samples showed antimicrobial activity, depending on the type of honey, concentration and strain analysed. The novelty of this study is given by the complex approach of the study of honey quality, both from the perspective of chemical attributes and the evaluation of the antimicrobial potential on specific strains in correlation with the botanical and geographical origin of the analyzed area.