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A new measure of the crystal-field strength, complementary to the conventional one, is defined. It is based on the rotational invariants |B_{k0}|_{av} or |sum_{k}B_{k0}|_{av}, k=2,4,6, of the crystal-(ligand)-field (CF) Hamiltonian H_{CF} parametrizations, i.e. on the axial CF parameters modules averaged over all reference frame orientations. They turn out to be equal to |H_{CF}^{(k)}|_{av} and |H_{CF}|_{av}, respectively. While the traditional measure is established on the parametrization modules or on the second moment of the CF energy levels, the introduced scale employs rather the first moment of the energy modules and has better resolving power. The new scale is able to differentiate the strength of various iso-modular parametrizations according to the classes of rotationally equivalent parametrizations. Using both the compatible CF strength measures one may draw more accurate conclusions about the Stark levels arrays and particularly their total splitting magnitudes.
To contribute to the understanding of noncovalent binding of halogenated molecules with a biological activity, electrostatic potential (ESP) maps of more than 2,500 compounds were thoroughly analysed. A peculiar region of positive ESP, called $sigma$
New charge transfer crystals of $pi$-conjugated, aromatic molecules (phenanthrene and picene) as donors were obtained by physical vapor transport. The melting behavior, optimization of crystal growth and the crystal structure is reported for charge t
We consider the problem of photon creation from vacuum inside an ideal cavity with vibrating walls in the resonance case, taking into account the interaction between the resonant field mode and a detector modeled by a quantum harmonic oscillator. The
Fe-gluconate, Fe(C_6H_11O_7_2xH_2O is a well-known material widely used for iron supplementation. On the other hand, it is used in food industry as a coloring agent, in cosmetic industry for skin and nail conditioning and metallurgy. Despite of wide
Nuclear Magnetic Resonance (NMR) spectroscopy is particularly well-suited to determine the structure of molecules and materials in powdered form. Structure determination usually proceeds by finding the best match between experimentally observed NMR c