Onur Şahin

4-hydroxy-2H-1,2-benzothiazine-3-carbohydrazide 1,1-dioxide-oxalohydrazide (1:1): X-ray structure and DFT calculations

The title compound, 4-hydroxy-2H-1,2-benzothiazine-3-carbohydrazide 1,1-dioxide-oxalohydrazide (1:1), is determined using X-ray diffraction techniques and the molecular structure is also optimized at the B3LYP/6-31G(d,p) level using density functional theory (DFT). The asymmetric unit consists of four independent molecules. The oxalohydrazide molecules have the centre of symmetry at the mid-point of the central C-C bond. Each thiazine ring adopts a half-chair conformation. Intermolecular C-H...O, N-H...O and N-H...N hydrogen bonds produce R22 (10), R22 (13), R33 (12) and R33 (15) rings, which lead to one-dimensional polymeric chains. An extensive three-dimensional supramolecular network of N-H...N, N-H...O, C-H...O and O-H...O hydrogen bonds is responsible for crystal structure stabilization.

Crystallographic Studies of Dehydration Phenomenon in Methyl 3-hydroxy-2-methyl-1,1,4-trioxo-1,2,3,4-tetrahydro-1λ6-benzo[e][1,2]thiazine-3-carboxylate

Methyl 3-hydroxy-2-methyl-1,1,4-trioxo-1,2,3,4-tetrahydro-1λ6-benzo[e][1,2]thiazine-3-carboxylate was synthesized in single step through in situ bromination of methyl 2-methyl-1,1,4-trioxo-1,2,3,4-tetrahydro-1λ6-benzo[e][1,2]thiazine-3-carboxylate using dibenzoyl peroxide & N-bromosuccinamide and was crystallized in acetone-ethyl acetate mixture (1:1). However, crystallization in methanol converted the title compound to methyl 3-methoxy-2-methyl-1,1,4-trioxo-1,2,3,4-tetrahydro-1λ6-benzo[e][1,2]thiazine-3-carboxylate, an unsymmetrical ether. The titled compound C11H11NO6S (3) crystallized in nonoclinic space group P21/c whereas, the compound C12H13NO6S (4) crystallized in triclinic space group P-1. X-ray studies shows that the molecules of 1 are linked into a one-dimensional framework structure by C–H···O and O–H···O hydrogen bonds, while in 4, intermolecular C–H···O and C–H···π hydrogen bonds and a π···π interaction result in the formation of infinite chains running along the [010] and [001] directions.Graphical Abstract

Chelate ring stacking interactions in the supramolecular assemblies of Zn(II)and Cd(II) coordination compounds: a combined experimental and theoretical study

The self-assembly of Zn(II) and Cd(II) ions with two isomeric tetradentate ligands, 2-pyridyl-isonicotinoylhydrazone (HL1) and 2-benzoylpyridyl-picolinoylhydrazone (HL2), was studied by elemental analysis, FT-IR spectroscopy and single-crystal X-ray diffraction. The reaction of zinc(II) and cadmium(II) salts with HL1 and HL2 in methanol under solvothermal conditions produced six monomer and one tetranuclear zinc(II) complexes, namely, Zn(HL1)Br2 (1), Zn(HL1)Cl2 (2), [Cd(HL1)2](NO3)2·H2O (3), Cd(HL2)Br2(4), Zn(HL2)Cl2 (5), Zn(HL2)Br2 (6) and [Zn4(L2)4I2][ZnI4]·2H2O (7). The structure of 7 includes a cationic tetranuclear cluster of four zinc ions, four ligands, and two anions, counterbalanced by ZnI42− ions. However, the reaction of zinc(II) and cadmium(II) salts with HL1 under the same conditions produced monomer compounds. Herein, the ligand effects on the complex structures were studied. Hirshfeld surface analysis and fingerprint plots facilitate the comparison of intermolecular interactions in compounds 1–7, which are crucial in building supramolecular architectures.

The synthesis, characterization, and theoretical hydrogen gas adsorption properties of copper(II)-3,3′-thiodipropionate complexes with imidazole derivatives

Three new coordination polymers, [Cu(μ3-tdp)(im)2]n (1), {[Cu(μ3-tdp)(1-mim)2]·0.5H2O}n (2) and {[Cu2(μ3-tdp)2(4-mim)4]·H2O}n (3) [tdpH2 = 3,3′-thiodipropionic acid, im = imidazole, 1-mim = 1-methylimidazole and 4-mim = 4-methylimidazole], have been prepared and characterized by spectroscopic techniques (IR and UV–Vis), elemental analyzes, magnetic measurements, thermal analyzes, and single-crystal X-ray diffraction. Complexes 1–3 crystallize in the monoclinic system with space groups of C2/c and P21/c, respectively. In 1–3, tdp is a bridging ligand to form 1-D chains, which are extended into a 2-D layer by hydrogen bonding and π···π interactions. The 3,3′-thiodipropionate exhibits an unexpected coordination mode in 1–3. Simulations were used to assess the potential of the complexes in H2 storage applications.

Hydrothermal synthesis, structural investigation, and magnetic properties of 2-D layered lanthanide (Ln = Pr, Eu, Gd, Tb, and Er) coordination polymers possessing infinite 1-D nanosized cavities

Five 2-D Ln(III) coordination polymers, [Ln(PDA)(PDAH)]n (PDA = 2,6-pyridinedicarboxylate), have been obtained under mild hydrothermal condition. In each coordination polymer, PDA is tetradentate and pentadentate, while lanthanides have coordination number eight to generate trigonal prismatic, triangular face bicapped LnO6N2 geometry having 9 triangular and 2 square faces. Two different types of bridging oxygens are responsible to grow the 2-D coordination polymers providing open channels possessing infinite 1-D nanosized cavities. Adjacent 2-D chains are further extended to a 3-D hydrogen-bonded layered network through intermolecular π–π interactions and C–H⋯O hydrogen bonds. Four lanthanides are arranged roughly at the vertices of a square and bridged by eight carboxylates leading to the overall tetrahedral shape of the secondary building units. The abnormal behavior of lanthanide contraction for the atomic radii of europium can be attributed to overlapping of electron clouds. The overall magnetic behavior is typical for the presence of antiferromagnetic exchange coupling interactions. Thermal decomposition analysis reveals that the coordination polymers have significant thermal stability. The coordination polymers are further characterized using elemental analysis and FT-IR spectroscopy. Tetrahedral SBUs to construct 2D net having nanosized cavities.

A new decavanadate polyoxovanadate nanocluster: synthesis, characterization and rapid adsorption of methylene blue

Abstract A new decavanadate polyoxovanadate nanocluster, [2-ampH]6[V10O28]∙2H2O (1), was synthesized through reaction between ammonium vanadate and 2-aminopyridine at pH = 2. Nanocluster 1 was characterized by IR, elemental analysis, and X-ray crystallography. 1 was found to adsorb and desorb dyes and may have widespread application in wastewater treatment. The utility of 1 for adsorption of methylene blue was studied. The adsorbed dyes can be easily desorbed, and 1 has full efficiency after five cycles.

Phthalocyanine and azaphthalocyanines containing eugenol: synthesis, DNA interaction and comparison of lipase inhibition properties

Novel eugenol-substituted zinc(II) azaphthalocyanines (ZnAzaPcs) were synthesised and their lipase inhibition and DNA binding properties compared with phthalocyanines (Pcs) containing eugenol. This is the first study on lipase inhibition and DNA binding of Pcs and AzaPcs containing a pharmacophore group, such as eugenol. The novel ZnAzaPcs were characterised using a combination of FT-IR,

Guaiacol Substituted AzaPCs: A Novel Synthesis Method and Investigation of Photophysical Properties

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