Publications by authors named "Mohamed Ghazzali"

A new paramagnetic ligand, 4-(2'-4-(2''-furyl)-pyrimidyl)-1,2,3,5-dithiadiazolyl (furylpymDTDA) and three transition metal coordination complexes, M(hfac)(furylpymDTDA) M=Mn, Co, Ni; hfac=1,1,1,5,5,5-hexafluoroacetylacetonato-), are reported. The solid-state structures are influenced by the geometry of the coordination sphere of the M(II) centers: trigonal (Mn) vs. octahedral (Co and Ni).

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New first-row transition-metal compounds with the ligand norharmane (9H-Pyrido[3,4-b]indole; Hnor) are reported. The compounds have the general formula [M(LL)(Hnor)(NO)](MeOH) (M=Co, Ni, Cu, Zn; LL=2,2'-bipyridyl (bpy), 1,10-phenanthroline (phen)) and have been characterized by physical and analytical methods. X-ray structural analysis revealed that the compound of formula [Cu(phen)(Hnor)(NO)], (1) has a distorted 6-coordinated octahedrally-based geometry, with a planar-based [CuNO] core, where Cu-L varies between 1.

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Three new compounds containing the bis(triphenylphosphane)iminium cation (PPN(+)) with ClO4(-), BF4(-) and [AgCl2](-) as counter anions have been synthesized and structurally characterized. The two derivatives with ClO4(-) and BF4(-) were found to be isostructural by single crystal X-ray diffraction. Interestingly, the three compounds show extremely potent antiproliferative effects against the human cancer cell line SKOV3.

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Four different-anion Ag(I) compounds with the ligand norharmane (9H-Pyrido[3,4-b]indole; Hnor) and having the general formula [Ag(Hnor)2](anion) (anion=ClO4(-), NO3(-) and BF4(-)) [Ag(Hnor)2(MeCN)](PF6) are reported, and studied in detail regarding their coordination mode and in vitro antiproliferative effects. X-ray structural analysis revealed that the complex with the PF6(-) anion has a MeCN solvent molecule weakly coordinated to Ag(I), making the metal coordination T-shaped, while the other compounds present the classical linear Ag(I) coordination. The compounds showed certain cell growth inhibitory effects in two different cancer cell lines, with the perchlorate containing complex being the most toxic and in fact comparable to cisplatin.

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Novel 6-aryl-2-methylnicotinic acid hydrazides 4a-c and their corresponding hydrazones 5a-c and 6a-i were synthesized. X-ray single crystal diffraction of 6h confirmed the chemical structure of hydrazones 6a-i. Antiproliferative activity of the synthetic compounds was investigated against K562 leukemia cell lines.

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3-Carb-oxy-pyridinium nitrate.

Acta Crystallogr Sect E Struct Rep Online

July 2012

In the crystal structure of the title compound, C(6)H(6)NO(2) (+)·NO(3) (-), the protonated cations are linked by N-H⋯O hydrogen bonds into chains along the b axis. The cations and anions are also linked by N-H⋯O and O-H⋯O hydrogen bonds. C-H⋯O inter-actions also occur.

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When the ligand 1,4,5-triazanaphthalene (abbreviated as tan) is reacted with Cu(II) BF(4)(-) and ClO(4)(-) salts, a variety of mononuclear compounds has been found, all with the [Cu(tan)(4)] unit and varying amounts of weakly coordinating axial ligands and lattice solvents. Reproducible compounds formed include two purple compounds, analyzing as [Cu(tan)(4)](ClO(4))(2)(CH(3)OH)(2)(H(2)O) (1) and [Cu(tan)(4)](BF(4))(2)(CH(3)OH)(1.5)(H(2)O) (3), and two blue compounds, analyzing as [Cu(tan)(4)](ClO(4))(2)(H(2)O)(2) (2) and [Cu(tan)(4)](2)(BF(4))(2)(H(2)O)(2) (4).

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2-Chloro-pyrimidin-4-amine.

Acta Crystallogr Sect E Struct Rep Online

February 2012

In the title pyrimidine derivative, C(4)H(4)ClN(3), the 2-chloro and 4-amino substituents almost lie in the mean plane of the pyrimidine ring, with deviations of 0.003 (1) Å for the Cl atom, and 0.020 (1) Å for the N atom.

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Both the acetyl and phenyl substituents of the central pyrazole ring in the title compound, C(24)H(20)N(2)O(3)S, are twisted with respect to the pyrazole ring, with the twist involving the phenyl ring being greater [67.4 (1) and 29.6 (2)°].

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In the title Schiff base, C(18)H(14)N(4)O, the amido -NH- unit is connected to one of the two pyridyl N atoms at an N(-H)⋯N distance of 2.624 (2) Å. The mol-ecular packing features an inter-molecular C-H⋯N R(2) (2)(6) hydrogen-bonding ring motif.

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In the title compound, [Fe(NCS)(2)(C(12)H(10)N(4))(CH(4)O)(2)](n), at 153 (2) K, the Fe atom is located on an inversion centre, as is the centre of the N-N bond in the ligand molecule. The structure contains a one-dimensional coordination polymer with an Fe..

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The title compound, [Ru(C(12)H(8)N(2))(3)](2)[Fe(NCS)(4)](ClO(4))(2), crystallizes in a tetragonal chiral space group (P4(1)2(1)2) and the assigned absolute configuration of the optically active molecules was unequivocally confirmed. The Delta-[Ru(II)(phen)(3)](2+) complex cations (phen is 1,10-phenanthroline) interact along the 4(1) screw axis parallel to the c axis, with an Ru..

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In the crystal structures of the title compounds, C(12)H(12)N(4)(2+).2BF(4)-, (I), and C(12)H(11)N(4)+.ClO(4)-, (II), respectively, infinite two- and one-dimensional architectures are built up via N-H.

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The title compound, [Cd(C(2)O(4))(C(3)H(7)NO)(2)](n), is isostructural with its Mn(II) analogue. The structure comprises zigzag polymeric chains with the oxalate groups situated on inversion centres and the Cd(II) atoms located on twofold rotation axes. The coordination geometry around Cd(II) is distorted octa-hedral and the intra-chain Cd⋯Cd distance is 5.

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