Chlorido[N′-(2-oxidobenzil­idene)acetohydrazide-κ2 O,N′,O′]copper(II) dihydrate

In the title complex, [Cu(C9H9N2O2)Cl]·2H2O, prepared from the Schiff base ligand N′-(2-hydroxy­benzil­idene)aceto­hydrazide and copper(II) chloride, the CuII atom is coord­inated by two O atoms and one N atom from the ligand and by a Cl atom in a distorted square-planar geometry. The two donor O atoms of the tridentate Schiff base ligand are in a trans arrangement. In the crystal structure, there is an extensive inter­molecular hydrogen-bonding network; N—H⋯O, O—H⋯O and O—H⋯Cl inter­actions, involving the uncoordinated water mol­ecules, lead to the formation of a two-dimensional network parallel to the ab plane

Synthesis and X-ray crystallography of (1R,3aR,7aR)-1-((S)-1-((2R,5S)-5-(3-hydroxypentan-3-yl)tetrahydrofuran-2-yl)ethyl)-7a-methyloctahydro-4H-inden-4-one

The crystal of the title compound, C21H36O3 contains an oxolane ring, and six defined stereocenters which are unambigously established by the crystallography study. A three dimensional supramolecular architecture is ensured by hydrogen bonds from the hydroxy group which is both engaged in inter (O-H···O2) and intramolecular C-H···O-H) hydrogen bonds. Weak C-H···O=C hydrogen bonds are involved also into the consolidation of the network

Bis(2-benzamido­benzimidazolato-κ2 N 1,O)(N,N-dimethyl­formamide-κO)copper(II)

In the title compound, [Cu(C14H10N3O)2(C3H7NO)], the CuII atom is five-coordinated by two N,O-bidentate 2-benzamido­benzimidazolate anions and one O-coordinated dimethyl­formamide (DMF) mol­ecule, resulting in a distorted square-based pyramidal CuN2O3 geometry for the metal atom, with the DMF O atom at the apical site. In the crystal structure, inter­molecular N—H⋯N hydrogen bonds result in chains of mol­ecules propagating along [100]

Bis(imidazole-κN 3)bis­(nitrato-κO)zinc(II)

The title complex, [Zn(NO3)2(C3H4N2)2], contains a ZnII centre with a slightly distorted tetra­hedral coordination environment, involving two N atoms from imidazole ligands and two O atoms from nitrate anions. The imino NH groups participate in inter­molecular N—H⋯O hydrogen bonds

1,2-Bis(N′-benzoyl­thio­ureido)benzene

The title compound, C22H18N4O2S2, was characterized by 1H and 13C NMR, solid-state IR spectroscopy and X-ray crystallographic techniques. The crystal structure determination reveals that the twisting modes of the two side arms are different [C—N—C—O and C—N—C—N torsion angles = −1.2 (3) and 1.1 (3)°, respectively, in one arm and 24.1 (3) and −5.1 (3)°, respectively, in the other]. The crystal structure involves N—H⋯O and N—H⋯S hydrogen bonds

N,N′-Dibenzyl-N′′-(4-bromo­benzo­yl)-N,N′-dimethyl­phospho­ric triamide

In the title compound, C23H25BrN3O2P, the P atom has a distorted tetra­hedral coordination. In the crystal structure, the mol­ecules form centrosymmetric dimers via pairs of essentially linear N—H⋯O hydrogen bonds

Lanthanide(III) complexes with tridentate Schiff base ligand, antioxidant activity and x-ray crystal structures of the Nd(III) and Sm(III) complexes

The tridentate N4-type Schiff base was synthesized from the condensation reaction of 2-hydrazinopyridine and pyridine-2-carbaldehyde. Neodymium and Samarium complexes were isolated when the corresponding nitrate salt was added to the solution of the ligand. The isolated compounds were characterized by elemental analyses, IR study, room temperature magnetic measurements and single X-ray crystal diffraction of the two crystals. Both complexes crystallize in the monoclinic system with space group P21/c. The cell parameters of the Nd complex are a=11.0927(8) Å, b=17.9926 (13) Å, c=11.9395(9)Å and β = 115.274(5) ° while the Sm complex shows parameters cell of a = 11.0477(8) Å, b = 17.9254(13) Å, c = 11.9149(8) Å and β =115.489(5) °. The X-ray study reveals isotopic Nd/Sm binuclear structures were each metal ion is nine-coordinated in the same fashion. Both metal centers have distorted tricapped trigonal prism geometry, with the Schiff base acting as tridentate ligand. The DPPH· radical scavenging effects of the Schiff base ligand and its Ln(III) complexes were screened. The Ln(III) complexes were significantly more efficient in quenching DPPH· than the free Schiff base ligand.Keywords: Lanthanide complexes, hydrazino, antioxidant activity, X-ray structur

4,6-Dimethyl-2-thioxo-1,2-dihydro­pyrimidin-3-ium chloride–thio­urea (1/1)

In the title compound, C6H9N2S+·Cl−·CH4N2S, the 4,6-di­methyl-2-thioxo-1,2-dihydro­pyrimidin-3-ium cation is proton­ated at one of the pyrimidine N atoms. The cations are bridged by the chloride anions through a pair of N—H⋯Cl hydrogen bonds. The amino groups of each thio­urea adduct inter­act with the chloride anions through a pair of N—H⋯Cl hydrogen bonds and the S atom of another thio­urea adduct through a pair of N—H⋯S hydrogen bonds. These inter­actions result in a layered hydrogen-bonded network propagating parallel to the bc plane. Except for two H atoms, all atoms are on special positions

Synthesis, physical studies and crystal structure determination of Y(III) and Er(III) complexes of 1-(pyridin-2-yl)-2-(pyridine-2-ylmethylene)hydrazine

Two isotype mononuclear yttrium(III) and erbium(III) complexes, {[Y(HL)(OAc)2(H2O)2]. (H2O)∙(NO3)} (1) and {[Er(HL) (OAc)2(H2O)2].(H2O)∙(NO3)} (2), where HL is the neutral Schiff base ligand 1-(pyridin-2-yl)-2-(pyridine-2-ylmethylene)hydrazine, and OAc is the acetate anion, have been synthesized and characterized by physicochemical methods and single crystal X-ray determination. Both complexes crystallizes in the triclinic space group Pī with unit cell dimensions for complex of Y(III) a = 7.909 (2) Å, b = 11.718 (4) Å, c = 12.497 (3) Å,    α = 78.907 (3)°, b = 73.840 (3)°, γ = 72.074 (3)°, V = 1051.26 (6) Å3, Z = 2, R1 = 0.051 and    wR2 = 0.112 and for complex of Er(III)a = 7.913 (1) Å, b = 11.719 (2) Å, c = 12.487 (2) Å,          α = 78.832 (1)°, α = 73.674 (1)°, γ = 72.012 (1)°, V = 1049.64 (3) Å3, Z = 2, R1 = 0.028, and   wR2 = 0.062. In both complexes, the coordination polyhedra around Ln(III) atoms are best described as a distorted tricapped trigonal prism. Antioxidant activities of the ligand and its Y(III) and Er(III) complexes are studied

Poly[di-μ-aqua-diaqua-di-μ6-malonato-cobalt(II)dipotassium(I)]

In the title complex, [CoK2(C3H2O4)2(H2O)4]n, the Co atom is located on a position with site symmetry 2/m, the K atom and one water mol­ecule are located on a mirror plane, and the malonate and one water mol­ecule are located on a twofold rotation axis. The KI atom is seven-coordinated by four carboxyl­ate O atoms from four malonate ligands and by three water O atoms, forming a distorted polyhedron. The CoII atom is in an almost octa­hedral environment formed by four carboxyl­ate O atoms from two malonate ligands and two water O atoms. The structure consists of layers parallel to (20) built up from edge-sharing KO7 and CoO6 polyhedra, which are connected by O—H⋯O hydrogen bonding including water mol­ecules into a three-dimensional network