Analysis of the fine structure of XANES spectra over Ni<Emphasis Type="Italic">K</Emphasis> edge in Ni(EtOCS<Subscript>2</Subscript>)<Subscript>2</Subscript>

The NiK edge X-ray absorption near edge spectra (XANES) of the Ni(EtOCS₂)₂ complex were measured. The theoretical NiK edge XANES spectra were calculated by the total multiple scattering and finite difference methods; the potential was calculated with a muffin-tin approximation and without it. It is shown that inclusion of the non-muffin-tin effects is important for modeling the NiK XANES spectrum for the Ni(EtOCS₂)₂ complex; good agreement with experiment was achieved only in the calculations with the total potential (without the muffin-tin approximation for the shape of the potential).     

Experimental and theoretical study of X-ray <Emphasis Type="Italic">K</Emphasis> edges absorption spectra of carbon and nitrogen in the phthalocyanine H<Subscript>2</Subscript>Pc molecule

The study of the electronic structure of H₂Pc was carried out to examine the structure of the lowest unoccupied molecular orbitals (LUMO) of molecule phthalocyanine by X-ray absorption spectroscopy using quantum-chemical calculations. The theoretical calculations were performed on the stationary theory (frozen orbital approximation, Z+1 model) and time-dependent density functional theory (TDDFT). A consideration of K edges absorption spectra of carbon and nitrogen in the common scale of binding energies allows estimating the contributions of AO of all phthalocyanine atoms to the LUMO, defining the sequence of levels, the binding energies of the corresponding levels, and also the character of electronic interactions between individual atoms. It was shown that the best agreement between the experimental and theoretical pre-edge structures of the absorption spectra of nitrogen and carbon for H₂Pc is observed in the case of the application of stationary density functional theory in Z+1 model to account for an X-ray hole. In this case the 2p _π AO of the Nα_(1,2) and Сα atoms make a predominant contribution to the LUMO. The 2p _π AO of the Nα_(1,2) atoms mainly contribute to the boundary LUMO with the energy ~–2.3 eV.     

Electronic structure and Mn<Emphasis Type="Italic">K</Emphasis> absorption spectra of MnO clusters in nanocomposites

The products of the thermobaric treatment (P = 1–4 GPa, T = 2000°C) of the ultrafine powder Re_0.67Rh_0.33 (crystallite size 50 Å) were studied. For one of the products, the (Vickers) microhardness is 1200 kg/mm², which is significantly higher than the literature values for alloys in the Re-Rh system. This effect is attributed to the formation of a binary carbide with an anti-NiAs type of structure.     

Molecular structure,vibrational spectra and potential energy distribution of protopine using <Emphasis Type="Italic">ab initio</Emphasis> and density functional theory

This work is devoted to theoretical study on molecular structure of protopine. The equilibrium geometry, harmonic vibrational frequencies and infrared intensities were calculated by ab initio Hartree-Fock and density functional B3LYP methods with the 6-31G(d) basis set and were interpreted in terms of potential energy distribution (PED) analysis. The internal coordinates were optimized repeatedly for many times to maximize the PED contributions. A detailed interpretation of the infrared spectra of protopine is reported. The calculations are in agreement with experiment. The thermodynamic functions of the title compound were also performed at HF/6-31G(d) and B3LYP/6-31G(d) level of theory. The FT-IR spectra of protopine were recorded in solid phase.