A luminescent zero-dimensional organic-inorganic hybrid indium halide (TUH)[InSbBr]Br (TU = thiourea, 0 ≤ ≤ 0.0998) was synthesized via the solvothermal method. In structures, resolved by single-crystal X-ray diffraction, isolated distorted [InBr] and [SbBr] octahedra are linked to organic TUH cations by intermolecular N-H···Br and N-H···S hydrogen bonds.
View Article and Find Full Text PDFThe primary aim of the study was to assess cerebral circulation in healthy young subjects during an ultra-short (45 min) session of ground-based microgravity modeled by "dry" immersion (DI), with the help of a multifunctional Laser Doppler Flowmetry (LDF) analyzer. In addition, we tested a hypothesis that cerebral temperature would grow during a DI session. The supraorbital area of the forehead and forearm area were tested before, within, and after a DI session.
View Article and Find Full Text PDFPhysical mechanisms underlying the multilevel resistive tuning over seven orders of magnitude in structures based on TiO/AlO bilayers, sandwiched between platinum electrodes, are responsible for the nonlinear dependence of the conductivity of intermediate resistance states on the writing voltage. To improve the linearity of the electric-field resistance tuning, we apply a contact engineering approach. For this purpose, platinum top electrodes were replaced with aluminum and copper ones to induce the oxygen-related electrochemical reactions at the interface with the AlO switching layer of the structures.
View Article and Find Full Text PDFDetecting the folding/unfolding pathways of biological macromolecules is one of the urgent problems of molecular biophysics. The unfolding of bacterial luciferase from is well-studied, unlike that of , despite the fact that both of them are actively used as a reporter system. The aim of this study was to compare the conformational transitions of these luciferases from two different protein subfamilies during equilibrium unfolding with urea.
View Article and Find Full Text PDFFeO@SiO core-shell nanoparticles (NPs) were synthesized with the co-precipitation method and functionalized with NH amino-groups. The nanoparticles were characterized by X-ray, FT-IR spectroscopy, transmission electron microscopy, selected area electron diffraction, and vibrating sample magnetometry. The magnetic core of all the nanoparticles was shown to be nanocrystalline with the crystal parameters corresponding only to the FeO phase covered with a homogeneous amorphous silica (SiO) shell of about 6 nm in thickness.
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