Structural and magnetic properties of the phase transition in absorbed and non-absorbed copper(II) trans-1,4-cyclohexanedicarboxylate

A large amount of toluene can be absorbed into the 1-dimensional tunnels in copper(II) trans-1,4-cyclohexane dicarboxylate (Cu(trans-1,4-OOCC₆H₁₀C)) at room temperature, and it can be desorbed by evacuation at elevated temperatures. The reversible absorption/desorption behavior of toluene was studied by magnetic susceptibility measurements using SQUID magnetometer and by powder X-ray diffractometry with high-energy synchrotron radiation at SPring-8, Japan. The first order phase transition was observed at 160 K in the magnetic susceptibility curve for the empty (non-absorbed or desorbed) sample, and the structural difference between the low and high temperature phases was detected in the powder X-ray diffraction patterns. On the other hand, no phase transition was observed in fully toluene-absorbed sample, and the structure was similar to that of the low temperature phase of the empty sample. The absorption/desorption behavior observed in the present study coincides with the results of heat capacity measurements by adiabatic calorimetry reported previously.     

New oxidized isocularine alkaloids from sarcocapnos plants

Structures 1a, 3 and 6 were deduced for the new oxoisocularine alkaloids, oxosarcophylline, yagonine and aristoyagonine, respectively, on the basis of spectroscopic studies and synthesis.     

Compound-forming effect for the electrical resistivity of liquid IVB-Te alloys

The resistivity isotherm of liquid IVb(Sn,Pb)-Te alloys has a remarkable maximum and temperature coefficient of resistivity has large negative value around the equiatomic composition, suggesting that a kind of compound formation exists at this composition. The excess resistivities are interpreted in terms of resonance scattering by the compound of MTe(M=Sn, Pb) with a finite life time.     

Coenzym-Modelle. 5. Mitt. Additionsreaktion des Cyanidions an monomere und polymere Nicotinamide Beziehung zwischen den Gleichgewichts-und Reaktionsgeschwindigkeiten

Ohne Zusammenfassung     

An alternative theorem for set-valued maps via set relations and its application to robustness of feasible sets

Abstract

This paper contains a generalized Gordan-type alternative theorem for set-valued maps which characterizes set relations without any convexity assumptions using certain evaluation functions. As a direct consequence and as a good example, we discuss robustness (or stability) of linear programming problems for modelling error. Moreover, this theorem can be utilized for that of general vector optimization problems in special cases due to reformation of the evaluation functions.     

High-resolution photoassociation spectroscopy of ultracold ytterbium atoms by using the intercombination transition

We observed high-resolution photoassociation spectra of laser-cooled ytterbium (Yb) atoms in the spin-forbidden 1S0 - 3P1 intercombination line. The rovibrational levels in the 0u+ state were measured for red detunings of the photoassociation laser ranging from 2.9 MHz to 1.97 GHz with respect to the atomic resonance. The rotational splitting of the vibrational levels near the dissociation limit were fully resolved due to the sub-MHz linewidth of the spectra in contrast to previous measurements using the spin-allowed singlet transition. In addition, from a comparison between the spectra of 174Yb and those of 176Yb, a d-wave shape resonance for 174Yb is strongly suggested.     

Microstructure of Milled Mesophase Pitch-Based Carbon Fibers as an Anode Material for Li-ion Batteries

Abstract

The microstructure of milled mesophase pitch-based carbon fibers (mMPCFs) that have been developed as an anode material for Li ion batteries have been studied as a function of heat treatment temperature (HTT), by SEM, X-ray diffraction, and Raman spectroscopy. And the results obtained are compared with those by X-ray diffraction (XRD) and SEM observations, for the characterization of specific structural features of mMPCFs as a promising anode material.     

Mechanistic study of photocatalytic CO2 reduction using a Ru(ii)–Re(i) supramolecular photocatalyst

Supramolecular photocatalysts comprising [Ru(diimine)₃]²⁺ photosensitiser and fac-[Re(diimine)(CO)₃{OC(O)OC₂H₄NR₂}] catalyst units can be used to reduce CO₂ to CO with high selectivity, durability and efficiency. In the presence of triethanolamine, the Re catalyst unit efficiently takes up CO₂ to form a carbonate ester complex, and then direct photocatalytic reduction of a low concentration of CO₂, e.g., 10% CO₂, can be achieved using this type of supramolecular photocatalyst. In this work, the mechanism of the photocatalytic reduction of CO₂ was investigated applying such a supramolecular photocatalyst, RuC2Re with a carbonate ester ligand, using time-resolved visible and infrared spectroscopies and electrochemical methods. Using time-resolved spectroscopic measurements, the kinetics of the photochemical formation processes of the one-electron-reduced species RuC2(Re)−, which is an essential intermediate in the photocatalytic reaction, were clarified in detail and its electronic structure was elucidated. These studies also showed that RuC2(Re)− is stable for 10 ms in the reaction solution. Cyclic voltammograms measured at various scan rates besides temperature and kinetic analyses of RuC2(Re)− produced by steady-state irradiation indicated that the subsequent reaction of RuC2(Re)− proceeds with an observed first-order rate constant of approximately 1.8 s⁻¹ at 298 K and is a unimolecular reaction, independent of the concentrations of both CO₂ and RuC2(Re)−.

Formation processes and reactivity of an important intermediate of photocatalytic CO₂ reduction, one-electron reduced species of a Ru(ii)–Re(i) supramolecular photocatalyst with a carbonate ester ligand, were investigated in detail.