Some Reactions of 5-(3 or 4-Pyridyl)-1,3,4-Oxadiazoles with Amines and Hydrazines

2-Amino-and 2-hydrazino-5-(3 or 4-pyridyl)-1, 3, 4-oxadiazoles [II_i-k] have been prepared by racting 2-chloro derivatives with the corresponding amines or hydrazines, the 2-hydrazino (II_i-k) compounds that obtained were heated with carbon disulphide and alcoholic potassium hydroxide where 5-(3 or 4-pyridyl)-1,3,4-oxadiazolo (2,3-C)-1,2,4-triazole 5-thione (III_a-c) were obtained, the given structures were biologically screened.     

THE REACTIONS OF N3P3CL6 AND RELATED COMPOUNDS WITH DIFUNCTIONAL REAGENTS. COMPARISONS AND CONTRASTS

Abstract

The reactions of N₃P₃Cl₆ with a variety of difunctional reagents are discussed. NMR spectroscopic and X-ray crystallographic investigations are presented.     

New Schiff base complexes of tetrachlorouranium

Summary Tetrachlorouranium complexes containing a Schiff base ligand, p-XC₆H₄NH=CHC₆H₄OH(L), derived from p-XC₆H₄NH₂ and salicylaldehyde, have been prepared. Atris complex was obtained when X=NO₂ andbis complexes for the other p-substituted Schiff bases when X=Cl, Br, OH and Me.     

The synthesis and ultraviolet spectra of some N-aryl-2,3-dihydro-3-oxo-4H-1,4-oxazine derivatives

Two new derivatives of the 1,4-oxazine ring system ( 3a and 3b ) derived from p-aminobenz-amides have been synthesized. The uv absorption spectra of sixteen representative 1,4-oxazines all show two high intensity bands (? ～ 10⁵) between 220-400 ran. The positions and intensities of the absorption maxima have been correlated with the steric and electronic effects of the oxazine ring substituents.     

Improved results on robust exponential stability criteria for neutral-type delayed neural networks

In this paper, we investigate the problem of robust global exponential stability analysis for a class of neutral-type neural networks. The interval time-varying delays allow for both slow and fast time-varying delays. The values of the time-varying uncertain parameters are assumed to be bounded within given compact sets. Improved global exponential stability condition is derived by employing new Lyapunov-Krasovskii functional and the integral inequality. The developed nominal and robust stability criteria is delay-dependent and characterized by linear-matrix inequalities (LMIs). The developed results are less conservative than previous published ones in the literature, which are illustrated by representative numerical examples.     

Semiempirical molecular orbital calculations of anisotropic 1H, 13C and 19F hyperfine coupling constants in hydrocarbon and fluorocarbon radicals

The anisotropic hyperfine coupling constants (AHCC) from the electron spin resonance (E.S.R.) spectra of a variety of atoms in organic radicals have been calculated by means of semiempirical molecular orbital wavefunctions in the INDO approximation. Hyperfine tensors involving ¹H, ¹³C and ¹⁹F nuclei are obtained for the ?H, ?H₃, CH₃?H₂, (CH₃)₃? hydrocarbon radicals, malonic acid radical, ?H₂F, ?F₂H, ?F₃ and CF₃?H₂ radicals. The calculated values are compared with available experimental, non-empirical and semiempirical values for these radicals. All integrals of the operator entering the electronic contributions have been evaluated over Slater type orbitals. The introduction of deorthogonalized wavefunctions gives generally better calculated results. In particular, the tensor components of the ¹⁹F AHCC are in good agreement with the experimental results without the necessity of readjusting the effective nuclear charges.