Preliminary study of the thermally stimulated blue luminescence of ulexite

In this paper, novel results on the blue thermally stimulated luminescence (TSL) emission of ulexite (NaCaB₅O₆(OH)₆·5H₂O) have been studied. The four maxima appearing at 60, 110, 200 and 240°C on the TSL glow curves of this borate could be respectively associated to: (i) the first dehydration (NaCaB₅O₆(OH)₆·5H₂O→NaCaB₅O₆(OH)₆·3H₂O), (ii) the creation-annihilation of the three-hydrated phase, (iii) the Na-coordinated chains dehydroxylation and the starting point of the alkali self-diffusion through the lattice and (iv) the amorphisation of the lattice. These results are fairly well correlated with the differential thermal analyses (DTA), in situ thermal observations under environmental scanning electron microscope (TESEM) and thermal X-ray diffraction (TXRD) techniques.     

Dynamic spin-orbit interaction of heavy ions in semiclassical calculations of elastic scattering

Experimental results of the 1st rank analyzing power for elastic scattering of⁶Li and⁷Li could be only understood when including coupling to inelastic channels in the calculations. This finding — established for some time — yet presents some open questions regarding the energy dependence of the spin and polarization effects. Semiclassical calculations presented here might clarify the relevant physical background of the earlier quantummechanically exact results.     

Semiclassical theory of analysing powers for polarised heavy-ion elastic scattering

A unified semiclassical theory of analysing powers of all ranks for polarised heavy-ion elastic scattering from a spin-zero target at energies above the Coulomb barrier is presented. Illustration is provided for by specialising to the two interactions, spin-orbit and tensor. The present approach recovers the phenomenological result, obtained by taking the difference of the nuclear overlap between unpolarised and aligned projectiles (shape-effect model), which successfully explained the structureless pattern of rank-2 observables for aligned ⁷Li + ⁵⁸Ni at E_lab ～ 20 MeV. Deviations observed for ⁷Li + ¹²C (oscillations) are interpreted as due to interference between diffraction (positive-angle) and negative-angle scattering terms.     

Titanium Dioxide/Electrolyte Solution Interface: Electron Transfer Phenomena

Electron transfer between a titanium dioxide/electrolyte solution interface has been studied. As found by other researchers of similar interfaces (TiO(2)- and ZnO-electrolyte solution), a slow consumption of OH(-) ions takes place in this type of interface. A theoretical model has been developed for calculating the change in the Fermi energy of both electrolyte solution and semiconductor, showing that ion consumption from the solution is favoured by the decrease of the difference between their Fermi energies. A kinetic constant (upsilon) is found to characterise the consumption process, its value increasing with electrolyte and semiconductor mass concentrations. Furthermore, this process may be used to estimate the point of zero charge of a titanium dioxide colloidal dispersion. Copyright 2000 Academic Press.     

Dichlorocarbene Addition to

In contrast to the terminal phosphinidene complex PhPW(CO)(5) (2), which adds to [5]metacyclophane (1) in a 1,4-fashion, dichlorocarbene preferentially adds in a 1,2-fashion to the formal "anti-Bredt" type double bond of the aromatic ring of 1 to afford the norcaradiene 11b, which immediately rearranges to the bridged cycloheptatriene 12b and further by a [1,5] sigmatropic chlorine migration to the isomeric 13b as the first observable product. More slowly, the latter isomerizes via a dissociative mechanism to give 15b. A computational study supports the notion that the [1,5] chlorine migration in the rearrangement 12b --> 13b, for which an activation barrier of 70.2 kJ mol(-)(1) was calculated, is essentially concerted with minor charge separation. In contrast, the analogous [1,5] chlorine migration in the flat model compound 7,7-dichlorocycloheptatriene (12a) displays features of a dissociative pathway.