Charge transfer states in GeO2-doped silicate fiber-optic waveguides and their role in second-harmonic generation

The concentration dependence of the broad-band luminescence arising in GeO₂-doped silicate fiber-optic waveguides is measured and interpreted. The spectra obtained show that electronic excitations of a new type that are absent in pure silicate glass — charge transfer excitons — arise in the doped system. Under the action of light an electron can be transferred both from a Ge center into the host and between Ge centers. Self-organization of these excitations in the field of a light wave (orientational ordering of their dipole moments) results in the appearance of a macroscopic electric field that destroys the initial centrosymmetry of the system and allows second-harmonic generation. Pis’ma Zh. éksp. Teor. Fiz. 68, No. 10, 737–740 (25 November 1998)     

Observation of an unprecedented Cu Bis-His site: crystal structure of the H129V mutant of nitrite reductase

Copper nitrite reductases contain both an electron-transfer type 1 Cu site and a catalytic type 2 Cu site. We have mutated one of the type 2 copper ligating histidines to observe the effect on catalytic turnover. This mutation has created a unique site where Cu is ligated by 2 His Nepsilon2 atoms alone.     

Dehydrogenation of methanol on low Cu and Re—Cu catalysts supported on sibunite

The activity and selectivity of mono- and bimetallic catalysts containing copper and rhenium on sibunite were studied in the decomposition of methanol to methyl formate (MF), water, H₂, CO, and CO₂at 200—400 °C. Methane is also formed on rhenium-containing catalysts at 300—400 °C. The dehydrogenating activity and selectivity to form MF are higher on the copper-sibunite catalysts than on the rhenium-sibunite samples. The introduction of 0.25% Re into the 4% copper-containing catalyst enhances its total activity and stability.     

Spectroscopic characterization of mineral crystals produced by the bacterium Azospirillum brasilense

The results of spectroscopic structural and trace elemental analyses of mineral crystals produced by the soil nitrogen-fixing bacterium Azospirillum brasilense cultivated in a synthetic medium are presented and discussed. The mineral formed is shown to have a structure close to struvite (MgNH(4)PO(4) x 6H(2)O; ASTM file No. 15-762) with some differences which may be attributed to the presence of isomorphic admixtures of other cations (struvite is known to have a variety of forms). AAS/AES and ion chromatography analyses for a number of biologically important microelements and their role in the formation of the crystal structure, as well as some questions related to biomineralization are also discussed.     

1H NMR and IR Spectroscopic Study of the Structure of the Major Component of the 99mTc HMPAO (Hexamethylpropyleneamino Oxime) Radiopharmaceutical Preparation

d,l-Hexamethylpropyleneamino oxime (HMPAO) was synthesized and isolated from a mixture of d,l - and meso-isomers. The structure of the conformers was studied using ¹H NMR spectroscopy over a broad range of pH. A method for estimating the amount of meso-form present in the mixture of isomers was proposed. It was shown that specific features of the IR spectra depend on the structure of the isomers and on the difference between the packing of molecules in the crystal lattice.     

Mathematical Model of Speeds Change Device on the Basis of Switched Differential Mechanisms

International Applied Mechanics - The geometry and kinematics of a dynamic system with several degrees of freedom and controllable friction clutches are considered. The necessary kinematic...