The shell model within the 2s1d0g7/20h11/2 shell is applied to calculate nuclear structure properties of the even Z = 52 − 62, N = 82 isotones. The results are compared with experimental data and with the results of a quasiparticle random-phase approximation (QRPA) calculation. The interaction used in these calculations is a realistic two-body G-matrix interaction derived from modern meson-exch...

Taking into account the notion of BL-general fuzzy automaton, in the present study we define the notation of BL-intuitionistic general L-fuzzy automaton and I-bisimulation for BL-intuitionistic general L-fuzzy automaton.Then for a given BL-intuitionistic general L-fuzzy automaton, we obtain the greatest I-bisimulation. According to this notion, we give the structure of quotient BL-intuiti...

la polymerisation thermique des huiles siccatives, en particulier l'huile de lin, semble etre une reaction bien connue . tandis que la structure des macromolecules n'est pas encore definie avec precision. on a montre que, lors de la standolisation de l'huile de jin, il se forme des aeides dimeres (c36) et trirneres (c54) , par le mecanisme de la synthese dienique, l'etude ex...

A flavonol, kaempferol, isolated from the fresh flower petals of C. sativus L. (Iridaceae) as the sole component. The structure of the compound was determined by chemical and spectroscopic methods.

A flavonol, kaempferol, isolated from the fresh flower petals of C. sativus L. (Iridaceae) as the sole component. The structure of the compound was determined by chemical and spectroscopic methods.

From the aerial parts of Tanacetum balsamita L. (Compositae) a flavonol aglycon was iso­lated using chromatographic techniques. The structure of this compound was determined using spectroscopic methods (UV, H-NMR and MS) as 3',4',5,7-Tetrahydroxy flavonol (Quercetin).

From the aerial parts of Tanacetum balsamita L. (Compositae) a flavonol aglycon was iso­lated using chromatographic techniques. The structure of this compound was determined using spectroscopic methods (UV, H-NMR and MS) as 3',4',5,7-Tetrahydroxy flavonol (Quercetin).