Infra-Red Spectra of the Nitrogen-15 Labelled Triphosphonitrilic Chloride

Although the vibrational spectra of triphosphonitrilic chloride, (PNCl₂)₃ (1), have been studied by numerous investigators^1–8, there is no general agreement about the frequency of completely inactive A₂ ring vibration. Besides, assignment of some overtones and combination bands is doubtful.     

Synthesis,structural characterization and anticancer properties of p-cymene Ru(II) complexes with 2-(N-methyl-1H-1,2,4-triazol-3-yl)pyridines

Transition Metal Chemistry - The structures of new p-cymene Ru(II) complexes with 2-(1-methyl-1H-1,2,4-triazol-3-yl)pyridine and 2-(1-methyl-1H-1,2,4-triazol-5-yl)pyridine were established based on...     

Order-Unity 13C Nuclear Polarization of [1-13C]Pyruvate in Seconds and the Interplay of Water and SABRE Enhancement

Signal Amplification By Reversible Exchange in SHield Enabled Alignment Transfer (SABRE-SHEATH) is investigated to achieve rapid hyperpolarization of ¹³C₁ spins of [1-¹³C]pyruvate, using parahydrogen as the source of nuclear spin order. Pyruvate exchange with an iridium polarization transfer complex can be modulated via a sensitive interplay between temperature and co-ligation of DMSO and H₂O. Order-unity ¹³C (>50 %) polarization of catalyst-bound [1-¹³C]pyruvate is achieved in less than 30 s by restricting the chemical exchange of [1-¹³C]pyruvate at lower temperatures. On the catalyst bound pyruvate, 39 % polarization is measured using a 1.4 T NMR spectrometer, and extrapolated to >50 % at the end of build-up in situ. The highest measured polarization of a 30-mM pyruvate sample, including free and bound pyruvate is 13 % when using 20 mM DMSO and 0.5 M water in CD₃OD. Efficient ¹³C polarization is also enabled by favorable relaxation dynamics in sub-microtesla magnetic fields, as indicated by fast polarization buildup rates compared to the T₁ spin-relaxation rates (e. g., ∼0.2 s⁻¹ versus ∼0.1 s⁻¹, respectively, for a 6 mM catalyst-[1-¹³C]pyruvate sample). Finally, the catalyst-bound hyperpolarized [1-¹³C]pyruvate can be released rapidly by cycling the temperature and/or by optimizing the amount of water, paving the way to future biomedical applications of hyperpolarized [1-¹³C]pyruvate produced via comparatively fast and simple SABRE-SHEATH-based approaches.     

Separation of 167Tm, 165Er and 169Yb from erbium targets irradiated by 60 MeV alpha particles

Journal of Radioanalytical and Nuclear Chemistry - Thin natEr2O3 targets were irradiated on cyclotron by 60 MeV alpha particles. Thulium and ytterbium radioisotopes, formed during...     

A Molecular Photosensitizer in a Porous Block Copolymer Matrix-Implications for the Design of Photocatalytically Active Membranes

Recently, porous photocatalytically active block copolymer membranes were introduced, based on heterogenized molecular catalysts. Here, we report the integration of the photosensitizer, i. e., the light absorbing unit in an intermolecular photocatalytic system into block copolymer membranes in a covalent manner. We study the resulting structure and evaluate the orientational mobility of the photosensitizer as integral part of the photocatalytic system in such membranes. To this end we utilize transient absorption anisotropy, highlighting the temporal reorientation of the transition dipole moment probed in a femtosecond pump-probe experiment. Our findings indicate that the photosensitizer is rigidly bound to the polymer membrane and shows a large heterogeneity of absolute anisotropy values as a function of location probed within the matrix. This reflects the sample inhomogeneity arising from different protonation states of the photosensitizer and different intermolecular interactions of the photosensitizers within the block copolymer membrane scaffold.     

Enhanced laser induced K X-rays generation during microchannel formation inside the object positioned in air

The increasing of yield of X-rays more than two times from femtosecond laser plasma produced in the target microchannel positioned in air compared to the case from fresh target’s surface was registered and the angular dependence of output of X-rays was firstly observed.     

On multiplicities of simple subquotients in generalized Verma modules

We reduce the problem on multiplicities of simple subquotients in an -stratified generalized Verma module to the analogous problem for classical Verma modules.     

Melting of ultrathin lubricant film due to dissipative heating of friction surfaces

Melting of an ultrathin lubricant film during friction between atomically smooth surfaces is studied. Additive noise of shear stress and strain as well as of film temperature is introduced and the phase diagram is constructed. On the diagram, the noise intensity for this temperature and the temperature of friction surfaces determine the regions of sliding, dry, and stick-slip friction. As a result of numerical analysis of the Langevin equation for various regions of the diagram, time series of stresses are constructed, which make it possible to explain the experiment on friction, in which intermittent motion is observed. Lubricant melting due to dissipative heating of friction surface is considered and the experimental time dependences of friction force are interpreted.     

Study of selective Fischer-Tropsch catalysts synthesized by the destruction of bimetallic carbonyl complexes on activated γ-Al2O3 support

The bimetallic catalysts obtained by the deposition of a Fe?Co binuclear cluster on the dehydroxylated γ-Al₂O₃ are studied and compared to some other relative systems. These bimetallic catalysts are found to be active and selective in olefin synthesis. This is connected with the formation of Fe?Co contact which is detectable by Mössbauer spectroscopy.