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A S Hilali

Publications and source records attributed to A S Hilali.

4 recordsLinked to original sources

Stereochemistry, structural and models of novel 5-(4'-derivatives phenyldiazo)-3-phenyl-2-thioxo-4-thiazolidinone complexes.

Copper(II) and cadmium(II) complexes of 5-(4'-derivatives phenyldiazo)-3-phenyl-2-thioxo-4-thiazolidinone (HLn) were prepared, their compositions and physicochemical properties were characterized by elemental analysis, magnetic suseptibility measurements, and infrared, electronic spectra. The novel complexes have the stoichiometric formulae [Cu(HLn)(OAc)n(H2O)(X)] (OAc = acetate, X = H2O or acetate) and [Cd(L)(OAc)(H2O)], respectively. Elemental analysis and IR spectra denote, that two types of complexes with different octahedral and tetrahedral structure for Cu(II) and Cd(II) ions. I.R. spectra show that the ligand is monobasic/neutral bidentate forming thereby a six-membered chelating ring and concomitant formation of an intramolecular hydrogen bond. The stoichiometeries of these complexes were determined conductometrically and indicated the formation of 1:1 and 1:2 (metal:ligand) complexes.

Azo Compounds↗

Substituents effect on the spectral studies on rutheninum(III) complexes of 5(-4'-derivatives phenyldiazo)-3-phenyl-2-thioxo-4-thiazolidinone.

A novel series of Ru(III) complexes with 5(-4'-derivatives phenyldiazo)-3-phenyl-2-thioxo-4-thiazolidinone (HLn) have been prepared. The ligands and structural composition of complexes were confirmed and characterized by various physico-chemical techniques. The spectral data were utilized to compute the important ligand field parameters B, beta and Dq. The effect of Hamett's constant on the ligand field parameters is also discussed. The spectral and magnetic results commensurate an octahedral environment around the Ru(III) ion. The B-values suggest a strong covalency in the metal-ligand sigma-bond and the Dq-values indicate a medium-strong ligand-field. IR spectra show that the ligand is neutral bidentate forming thereby a six-membered chelating ring and concomitant formation of an intramolecular hydrogen bond. The ligands are present in associated form in solution via intermolecular hydrogen bond and act as neutral bidentate coordinated to ruthenium(III).

Chemical Phenomena↗

Structural and models of dioxouranium(VI) with rhodanine azodyes--V.

The synthesis of several new coordination compounds of dioxouranium(VI) heterochelates with bidentate rhodanineazol compounds derived from rhodanine are described. The ligands and uranyl complexes have been charcaterized by various physico-chemical techniques. The bond lengths and the force constants have been calculated from asymmetric stretching frequency of O-U-O group. The infrared spectral studies showed a monobasic bidentate behaviour with the oxygen and azonitrogen donor system. The ligands contain intramolecular hydrogen bonds.

Electrons↗

Clicking hyoid.

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