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The interaction of dibutyltin(IV) dichloride (DBT) with 1,4-diazacycloheptane (homopiperazine, HP) was investigated. In solutions, the complexes formed a 1:1 complex, its protonated and hydrolyzed forms. The formation constants of the complexes and thermodynamic parameters as ΔH° and ΔS° were estimated. The optimization of the structure of the (Bu)2Sn(HP)Cl2 complex reveals that the tin is six-coordinate in a distorted octahedral geometry, where the two nitrogen atoms of homopiperazine and the two chloride ions are in one plane. The solid (Bu)2Sn(HP)Cl2 complex with homopiperazine was synthesized, and the composition was assigned by elemental micro-analysis and mass spectrum. The complex was investigated by infrared, mass spectra, and thermal measurements. The ligand and its complex were tested against antimicrobial Staphylococcus aureus (+ve), Escherichia coli (−ve), and antifungal Candida albicans and Aspergillus flavus. Anticancer activities of homopiperazine and its dibutyltin(IV) complex were tested against breast cancer cell lines. The molecular docking investigations were performed to know the possible modes of binding to the most active sites of the breast cancer oxidoreductase receptor and those of Escherichia coli. [ABSTRACT FROM AUTHOR]

Pd(BHEP)Cl2was synthesized and characterized (BHEP = 1,4-bis(2-hydroxyethyl)piperazine). The complex decomposes in two steps, leaving a residue of palladium metal. Amino acid ester (L) reacts with [Pd(BHEP)(H2O)2]2+(BHEP = 1,4-bis(2-hydroxyethyl)piperazine), giving mixed-ligand complexes, [Pd(BHEP)L]2+. The kinetics of hydrolysis of [Pd(BHEP)L]2+have been studied by pH-stat technique, and rate constants were obtained. Rate acceleration observed for glycine methyl ester is high. The effect with methionine methyl ester is much less marked, as the mixed-ligand complexes with these ligands do not involve alkoxycarbonyl donors. Possible mechanisms for these reactions are considered. The thermal stability of Pd(BHEP)Cl2complex was investigated. The role of the complex in the catalysis of amino acid esters was studied. [ABSTRACT FROM AUTHOR]

The complex formation equilibria in the reaction of [Pd(en)(H2O)2]2+with 4,4′-bipiperidine (Bip) and DNA constituents such as inosine, inosine-5′-monophosphate, uracil, uridine, thymine, and thymidine were investigated at 25 °C and 0.1 M ionic strength. The [(H2O)(en)Pd(Bip)Pd(en)(H2O)]4+complex and its hydrolyzed species were formed. Substitution of coordinated water by inosine (Ino) as DNA constituent formed the complexes [(Ino)(en)Pd(Bip)Pd(en)(H2O)]3+and [(Ino)(en)Pd(Bip)Pd(en)(Ino)]2+. The formation of the binuclear complexes was further supported by spectral measurements. The formation constants of all possible mono- and binuclear complexes were determined and their speciation diagrams were evaluated. Binuclear complexes involving 4,4′-bipiperidine linkage of two Pd(en)2+species were investigated. The binding of DNA constituents to the binuclear complex was studied. [ABSTRACT FROM AUTHOR]