Infrared spectra and relative stability of the F3CH/NH3 H-bonded complex in liquefied Xe

FTIR spectra of mixtures of fluoroform (F3CH) and ammonia (NH3), have been studied in liquid xenon between 5400 and 500 cm-1. Spectroscopic evidence for the formation of a hydrogen bonded complex has been found and the complexation enthalpy Delta(LXe)H degrees in the temperature interval between 173 and 215 K, was determined to be 14.4 (7) kJ mol-1. The parallel fundamentals nu1 and nu2 of ammonia reveal a strong narrowing effect upon complex formation, whereas the perpendicular fundamentals nu3 and nu4 show a modest decrease of their width. CP corrected ab initio calculations at the MP2(FULL)/6-311++G(3df,2pd) level predict a linear geometry for the complex, characterized by a small red shift of the CH stretch frequency of fluoroform. The ab initio interaction energy was found to be compatible with the isolated molecule complexation energy extrapolated from the experimental Delta(LXe)H degrees .     

A cryosolution infrared study of the complexes of fluoroform with ammonia and pyridine: Evidence for a C-H...N pseudo blue-shifting hydrogen bond

Mid-infrared spectra of mixed solutions in liquid xenon containing fluoroform and either ammonia or pyridine have been investigated at temperatures between 173 and 213 K. For both Lewis bases, a new band is found in the CH stretching region at a frequency approximately 5 cm(-1) higher than that of monomer fluoroform, which is assigned to a complex between fluoroform and the Lewis base. A detailed analysis of the nu1/2nu(4) Fermi resonance in the proton donor shows that the blue shifts observed for the complexes are not caused by a strengthening of the CH bond during the complexation, but are due to the changes in the Fermi resonance interactions. Information on the nu1/2nu(4) Fermi resonance was also obtained for the complexes of fluoroform with dimethyl ether and trimethyl amine.     

Radiation-Induced Heterogeneous Processes of Water Decomposition in the Presence of Mixtures of Silica and Zirconia Nanoparticles

The radiation-induced heterogeneous processes of water decomposition on mixtures of silicon dioxide (n-SiO₂) and zirconium dioxide (n-ZrO₂) nanoparticles have been studied. The kinetics of buildup of molecular hydrogen in the radiolytic processes of water decomposition in the test systems has been examined. The reaction rates and the radiation-chemical yield of hydrogen in the radiolysis of water in the presence of n-SiO₂–n-ZrO₂ mixtures with different ratios between the components have been determined. It has been found that the rates and radiation-chemical yields decreased on going from n-ZrO₂ to n-SiO₂. The individual components (n-SiO₂ and n-ZrO₂) and the mixtures of n-SiO₂–n-ZrO₂ and n-SiO₂–n-ZrO₂ + H₂O before and after γ-irradiation have been examined by Fourier-transform IR spectroscopy in order to reveal interactions between the components and to study the mechanism of radiolytic processes. It has been found that the adsorption of water in the test systems occurs via both molecular and dissociative mechanisms. It has been shown that there is no noticeable interaction between the components of the oxide nanoparticles under the conditions of the experiments.     

Shape of the IR bands of CH4: The CH4-Kr system in different phase states

The IR absorption spectrum of mixtures of CH₄ with Kr in the range 800–6000 cm^?1 is studied in the region of the gas-liquid and liquid-crystal phase transitions. It is found that, as the system density increases, the ratio of the ν₄ band intensity to that of the ν₃ band becomes larger and the measured values of the second spectral moment of the ν₄ band become smaller than the corresponding calculated values. The quantum counterpart of the generalized J-diffusion model was used to describe the shape of the ν₃ and ν₄ bands, and the rotational relaxation times of CH₄ in solutions were obtained. It was shown that, as the density increases, a broad 1470-cm^?1 band appears in the region of the “forbidden” (induced by a Coriolis interaction) ν₂ band (ν_Q=1535 cm^?1) detected in a low-density gas. The intensity of this band is appreciably higher than that of the ν₂ band.     

IR spectra of halothane–acetone complex in liquefied noble gases (Kr and Xe)

The interaction of semiconductor quantum dots and silver nanoparticles (AgNPs) with bacteriorhodopsin (BR), a membrane protein contained in the purple membrane (PM) of Halobacterium salinarum, is studied. It is shown that both types of nanoparticles are adsorbed efficiently on the surface of the purple membranes, modulating the parameters of the bacteriorhodopsin photocycle. Electrostatic interactions are found to be the main cause of the effect of nanoparticles on the bacteriorhodopsin photocycle. These results explain our earlier data on the “fixation” of the bacteriorhodopsin photocycle for protein molecules trapped after incubation of the purple membranes with silver nanoparticles near the location of the “hot spots” of the effect of surface-enhanced Raman scattering (SERS). It is demonstrated that exposure of silver nanoparticles with bacteriorhodopsin in SERS-active regions lowers the amount of bacteriorhodopsin molecules involved in phototransformations.     

FTIR Cryospectroscopic Study of Fermi Resonance Polyads νs ≈ 2νb in CHF3

Optics and Spectroscopy - The sequences of Fermi resonances νs ≈ 2νb in the IR spectrum of a fluoroform solution (CHF3) in liquefied krypton have been studied. Here, νs is the...     

Pyrogallol azo derivatives as analytical reagents for determining nickel(II)

Reagents based on bis-(2,3,4-trihydroxyphenylazo)benzidine and 2,2′,3,4-tetrahydroxy-3′-sulfo-5′-nitroazobenzene were used for the spectrophotometric determination of nickel. The optimum complexation conditions were found and the stability constants of the nickel complexes were determined. The effect of foreign ions and masking substances on the complexation was studied. The procedure was used for the photometric determination of nickel in volcanogenic rocks.     

IR spectroscopy study of the radiation-thermal decomposition of water on nanosized zirconium dioxide

Radiation-thermal decomposition of water on nanosized ZrO₂ in the temperature range of 300–673 K has been studied by FTIR spectroscopy. It has been revealed by the X-ray diffraction method that the sample used has the centrsymmetric monoclinic crystal structure. It has been shown that nanosized zirconium dioxide adsorbs water on via the molecular and dissociative mechanisms. Intermediate products of the radiation-induced heterogeneous decomposition of water, namely, the molecular oxygen and hydrogen peroxide radical ions, zirconium hydride, and hydroxyl radicals have been detected. A comparative analysis of changes in the absorption bands of molecular water and surface hydroxyl groups with temperature has been conducted, and the stimulating role of radiation in the radiation-thermal process of water decomposition has been revealed.