Über koordinativ ungesättigte Nickelkomplexe der Formazylreihe

Zusammenfassung Es wird die Darstellung einiger koordinativ ungesättigter Nickelkomplexe der heterocyclischen Formazylreihe beschrieben.     

Structural resolution of the stereochemistry of a spirooxirane derived from an α-arylidene heterocyclic carbonyl. The crystal and molecular structure of 2-(p-chlorophenyl)-5-phenyl-7-methyl-1-oxa-5,6-diazaspiro[2.4]hept-6-en-4-one

The stereochemical assignment of molecular geometry for α-arylidene carbonyl compounds and spirooxirane derived from them have continued to be a challenging problem for which the most satisfactory solution continues to be an x-ray diffraction structure determination. In that regard, the title compound (a spirooxirane) has been found to crystallize in the monoclinic space group P2_1/c with cell dimensions of a = 5.989(1)Å, b = 27.625(4)Å, c = 9.374(2)Å, β = 99.06(1)°. The structure of the compound has been determined, with the refinement to R = 0.059. The previous, tentative assignment of structure has been confirmed substantiating our prediction that the oxidation of the enone system proceeds with rotation of the phenyl group on the β-carbon away from the carbonyl group, minimizing adverse steric interactions and allowing orbitals of the carbonyl group to overlap with those of the carbanionic center during the closure of the oxirane ring. The agreement between predictions based on nmr data and the x-ray diffraction determination will support a stronger reliance on the nmr data predictions in subsequent studies.     

Twisted Orlicz algebras,II

Let G be a locally compact group, let be a 2‐cocycle, and let () be a complementary pair of strictly increasing continuous Young functions. We continue our investigation in [14] of the algebraic properties of the Orlicz space with respect to the twisted convolution ? coming from Ω. We show that the twisted Orlicz algebra posses a bounded approximate identity if and only if it is unital if and only if G is discrete. On the other hand, under suitable condition on Ω, becomes an Arens regular, dual Banach algebra. We also look into certain cohomological properties of , namely amenability and Connes‐amenability, and show that they rarely happen. We apply our methods to compactly generated group of polynomial growth and demonstrate that our results could be applied to variety of cases.     

Pretreatment,Anaerobic Codigestion,or Both? Which Is More Suitable for the Enhancement of Methane Production from Agricultural Waste?

Pretreatment and codigestion are proven to be effective strategies for the enhancement of the anaerobic digestion of lignocellulosic residues. The purpose of this study is to evaluate the effects of pretreatment and codigestion on methane production and the hydrolysis rate in the anaerobic digestion of agricultural wastes (AWs). Thermal and different thermochemical pretreatments were applied on AWs. Sewage sludge (SS) was selected as a cosubstrate. Biochemical methane potential tests were performed by mixing SS with raw and pretreated AWs at different mixing ratios. Hydrolysis rates were estimated by the best fit obtained with the first-order kinetic model. As a result of the experimental and kinetic studies, the best strategy was determined to be thermochemical pretreatment with sodium hydroxide (NaOH). This strategy resulted in a maximum enhancement in the anaerobic digestion of AWs, a 56% increase in methane production, an 81.90% increase in the hydrolysis rate and a 79.63% decrease in the technical digestion time compared to raw AWs. On the other hand, anaerobic codigestion (AcoD) with SS was determined to be ineffective when it came to the enhancement of methane production and the hydrolysis rate. The most suitable mixing ratio was determined to be 80:20 (Aws/SS) for the AcoD of the studied AWs with SS in order to obtain the highest possible methane production without any antagonistic effect.     

The activity structure of technology-based mathematics lessons: a case study of three teachers in English secondary schools

ABSTRACT

This article examines patterns of classroom organisation and interaction associated with the use of a particular type of digital technology – the dynamic software GeoGebra – in the lessons of an opportunity sample of three English secondary-school mathematics teachers. The concept of activity structure is used to organise this study, further informed by the concept of instrumental orchestration. While the case study analysis identifies structures already reported in those earlier papers, it also draws attention to the prevalence of a Predict-and-test format in tasks carried out by students at the computer. This study also shows how synthesising the activity structure and instrumental orchestration frameworks may be productive.     

Quantitavive Proton Magnetic Resonance Analysis of Ranitidine in Solid Dosage Forms

A rapid and specific proton magnetic resonance (PMR) spectroscopic method was developed for determining ranitidine hydrochloride in tablets. 2-Choloroacetophenon was used as the internal standard and DMSO-d₆ served as the PMR solvent. The concentration of drug per unit dose was calculated from the integration values for the resonance signals of ranitidine hydrochloride at 4.32 δ ppm and int. st. at 5.19 δ ppm. The method using commercial products gave comparable results to those obtained by the methods of UV spectroscopy and USP XXIII.     

Decay Pion Spectroscopy of Electro-Produced Hypernuclei

The investigation of light hypernuclei is quite important for understanding the basic YN interaction and the mechanism of hypernuclear structure. We started the commissioning of the decay pion spectroscopy of light hypernuclei at MAMI-C in 2011. In order to realize the K⁺ tagging efficiently, some detectors on KAOS spectrometer were upgraded or newly installed. The existing and well-studied spectrometers, SpekA, SpekC were used as pion spectrometers. The analysis is ongoing to estimate the detectors performance and develop the spectrometers for future experiments with higher beam intensity. The preliminary results of the particle identification are presented in this article.     

Investigation of the kinetics of OH∗ and CH∗ chemiluminescence in hydrocarbon oxidation behind reflected shock waves

The temporal variation of chemiluminescence emission from OH^?(A² Σ ⁺) and CH^?(A² Δ) in reacting Ar-diluted H₂/O₂/CH₄, C₂H₂/O₂ and C₂H₂/N₂O mixtures was studied in a shock tube for a wide temperature range at atmospheric pressures and various equivalence ratios. Time-resolved emission measurements were used to evaluate the relative importance of different reaction pathways. The main formation channel for OH^? in hydrocarbon combustion was studied with CH₄ as benchmark fuel. Three reaction pathways leading to CH^? were studied with C₂H₂ as fuel. Based on well-validated ground-state chemistry models from literature, sub-mechanisms for OH^? and CH^? were developed. For the main OH^?-forming reaction CH+O₂=OH^?+CO, a rate coefficient of k ₂=(8.0±2.6)×10¹⁰ cm³?mol^?1?s^?1 was determined. For CH^? formation, best agreement was achieved when incorporating reactions C₂+OH=CH^?+CO (k ₅=2.0×10¹⁴ cm³?mol^?1?s^?1) and C₂H+O=CH^?+CO (k ₆=3.6×10¹²exp(?10.9 kJ?mol^?1/RT) cm³?mol^?1?s^?1) and neglecting the C₂H+O₂=CH^?+CO₂ reaction.     

Molecular structure and EPR spectra studies of saccharinate complexes with 4-acetylpyridine

The crystal structures of [Co(4-acpy)₂(H₂O)₄] (sac)₂ (1) and [Zn(4-acpy)₂(H₂O)₄] (sac)₂ (2) (4-acpy: 4-acetylpyridine, sac: saccharinate) complexes have been investigated by X-ray diffraction techniques. The magnetic environments of Cu²⁺ doped [Co(4-acpy)₂(H₂O)₄] (sac)₂ and [Zn(4-acpy)₂(H₂O)₄] (sac)₂ complexes have been identified by electron paramagnetic resonance (EPR) technique. Principal values of g and hyperfine tensors are determined and the ground state wave functions of Cu²⁺ ions are obtained using EPR parameters. The vibrational spectra were also discussed in relation with the other compounds containing saccharinate and 4-acetylpyridine complexes.     

Microstructural and superconducting properties of C6H6 added bulk MgB2 superconductor

The effect of aromatic hydrocarbon (benzene, C₆H₆) addition on lattice parameters, microstructure, critical temperature (T_c), critical current density (J_c) of bulk MgB₂ has been studied. In this work only 2 mol% C₆H₆ addition was found to be very effective in increasing the J_c values, while resulting in slight reduction of the T_c. J_c values of 2 mol% C₆H₆ added MgB₂ bulks reached to 1.83×10⁶ A/cm² at 15 K and 0 T. Microstructural analyses suggest that J_c enhancement is associated with the substitution of carbon with boron and which also results in the smaller MgB₂ grain size. The change in the lattice parameters or the lattice disorder is claimed as a cause of the slight reduction in the T_c by carbon addition. We note that our results show the advantages of C₆H₆ addition include homogeneous mixing of precursor powders, avoidance of expansive nanoadditives, production of highly reactive C, and significant enhancement in J_c of MgB₂, compared to un-doped samples.