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A trinuclear copper complex [Cu3(napxshz)2(phen)2] has been synthesised using a tribasic naproxen‐appended ligand [H3napxshz = 2‐hydroxy‐N′‐(2‐[6‐methoxynaphthalen‐2‐yl] propanoyl) benzohydrazide] and 1,10‐phenanthroline. The complex was characterised by different spectroscopic methods such as Fouriertransform infrared (FT‐IR), ultraviolet‐visible (UV–Vis) and electrospray ionisation (ESI)‐mass spectroscopy. The solid‐state structure of the ligand and complex 1 was established by single‐crystal X‐ray diffraction analysis. The interaction of the complex and the ligand with DNA was investigated by UV–visible spectroscopy and fluorometric titrations. The calculated binding constants (Kb) of the complex and the ligand with ct‐DNA show that the complex has a higher binding affinity than the ligand H3napxshz. Quantum chemical calculations were performed to understand the structural aspects of the complex and its interactions with DNA. The molecular docking study reveals the interaction between DNA, and the complex is in intercalative mode. [ABSTRACT FROM AUTHOR]

Abstract: Phase behavior of sodium oleate (NaOl)/isoamyl alcohol‐based lamellar gel phase in cedar oil/water medium in the presence of the nonionic polymer hydroxyethyl cellulose (HEC) and its hydrophobic modified product (HMHEC) is investigated for the development of polymer‐embedded surfactant gels. HMHEC is more soluble in oil‐in‐water (o/w) microemulsions, but nonionic HEC shows limited solubility in the lamellar microemulsion (o/w type). Quantitative estimation of rate of adsorption of the polymer on lamellae bilayers can be easily done by Sudan solubilization and methylene blue complexation methods. Addition of HMHEC to the lamellar gel phase increases the polymer solubilization limit of lamellar gels as well as the viscoelasticity and thermal stability. The polymer‐embedded microemulsion gel acts as a “clean gel” since it exhibits good solubilization in different hydrocarbon media at ambient conditions. Elastic modulus of the polymer‐embedded gel influences directly the suspension performance of gels at high temperature and yields a reasonable sand‐settling velocity acceptable according to fracturing standards. The thermal characteristics and viscoelastic properties of polymer‐embedded gel were found to be suitable for moderate‐temperature reservoir stimulation where the bottom hole temperature is in the range 70–75 °C. Already a large amount of experimental data on pure microemulsions (without polymer) exists. Our studies indicate that the developed polymer‐embedded microemulsion gel has great potential as a model system for the study of polymer–microemulsion interactions. [ABSTRACT FROM AUTHOR]

A supramolecular compound, catena-poly{[Cu2(1,3-μ2-(1 a))2(μ2-ter)2(H2O)2] n·(6H2O) n} (1) has been synthesized using (1 a) [(1 a = N1, N3, N5-trimethyl- N1, N3, N5-tris((pyridin-4-yl)methyl)-1,3,5-benzene tricarboxamide] and terephthalate (ter) as the pillaring unit by self-assembly. The terephthalate units are connected by copper(II) ions forming a single strand, while a pair of such strands are then linked by (1 a) via two pyridyl terminal arms bound to copper(II) nodes on either side forming a one-dimensional double stranded assembly propagating along the c axis. The compound crystallizes in the Fdd2 space group. The cavity created in the interior of this double strand assembly trap six water molecules and are stabilized by hydrogen bonding with the host. The arrangement of the pair of acyclic water trimers in isolated cavities of (1) is such that it resembles a closed-bracket-like formation. The Hirshfeld surface analysis of (1) reveals the presence of strong intermolecular hydrogen-bonding interactions between one-dimensional ladder-like units and with the water trimer in the host cavity. The copper(II)-containing coordination polymer also acts as an efficient catalyst for the Glaser-Hay homo-coupling reaction. [ABSTRACT FROM AUTHOR]

Discusses the coordination chemistry of thiosemicarbazones, due to their interesting physicochemical and biological properties. Means in which the thiosemicarbazones act as chelating ligands with copper (II) ion; Arrangement of two inversion-symmetry-related monomers; Coordination of the azomethine nitrogen atom to the central copper (II) ion.

A coordination driven Pd2LIG4 self-assembly is synthesized using a new semi rigid dipodal ligand. [ABSTRACT FROM AUTHOR]

In the title centrosymmetric binuclear complex, [V2(C17H17N4S)2O4], pairs of V atoms are linked by two oxo bridges. The coordination geometry at each VV atom is distorted octa­hedral, involving a pyridine N atom, a thiol­ate S atom, an azomethine N atom from the 1-[phen­yl(2-pyrid­yl)methyl­ene]-2-(pyrrolidin-1-ylthio­carbon­yl)hydrazine(−) ligand, and one terminal O and 2 bridging O atoms. The crystal structure is stabilized by weak inter­molecular C—H⋯O inter­actions. [ABSTRACT FROM AUTHOR]

The title compound, [Cu2(C17H17N4S)2Cl2], exhibits a dimeric structure related by a centre of symmetry. The monomers are linked to each other by the longest Cu-S apical distance observed to date among Cu(II) square-pyramidal complexes of N4-substituted thiosemicarbazones. Each Cu(II) atom deviates from the coordination square plane, which contains the pyridyl and imine N atoms, the thiolate S atom and the Cl- anion, towards the S atom of the adjacent monomer. The dimers pack in a zigzag manner through the crystal.