Syntheses, Characterization, Crystal Structures and Antimicrobial Activity of Schiff Base Copper(II) Complexes Derived from 2-Bromo-6-((2-(isopropylamino) ethylimino)methyl)phenol

Three new copper(II) complexes, [Cu(LH)2]Br2 (1), [Cu(LH)2]NCS2 (2), and [Cu(LH)2](NO3)2 (3), where LH is the zwitterionic form of 2-bromo-6-((2-(isopropylamino)ethylimino)methyl)phenol (HL), were synthesized and characterized by elemental analysis, IR and UV-vis spectroscopy. The structures of the complexes were further confirmed by single crystal X-ray structure determination. All compounds are mononuclear copper(II) complexes. The Cu atoms in the complexes are coordinated by two imino N and two phenolate O atoms from two LH ligands, forming square planar coordination. The compounds were assayed for their antimicrobial activities.

Synthesis and Spectral Studies of Some Homo Dinuclear Lanthanide(III) Complexes of a Mesogenic Schiff Base

A mesogenic Schiff base, N,N’-di(4-decyloxysalicylidene)-1’,8’-diamino-3’,6’-dioxaoctane (H2L) and a series of homo dinuclear lanthanide(III) complexes of the type [Ln2(LH2)3(NO3)4](NO3)2, (Ln = La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, and Ho) were synthesized and characterized by elemental analysis, mass spectrometry, FTIR, and NMR spectral techniques. The IR and NMR spectral evidences imply bonding of a neutral bidentate H2L species through two phenolate oxygen atoms in its zwitterionic form to LnIII, rendering the overall geometry of the complexes as a seven-coordinate polyhedron – possibly distorted mono-capped octahedron. Differential scanning calorimetry (DSC) and polarizing optical icroscopic (POM) studies reveal mesogenic properties (smectic-X, smectic-A and nematic mesophases) in the ligand over a wide range of temperature but none mesomorphism in the LnIII complexes synthesized under this study. Luminescence studies exhibit emissions of H2L and TbIII complex.

Study on Interaction of Carboxylic Acid Gemini Surfactant with Cocamidopropyl Betaine in Aqueous Solution

The interaction of carboxylic acid gemini surfactant 4,8-didodecyl-3,9-dioxo-6-hydroxy-4,8-diaza-1,11-undecanedicarboxylic acid (CGS12) with amphoteric surfactant cocamidopropyl betaine (CAPB) at 258C and pH 7.0 has been investigated using pH titration, surface tension, dynamic light scattering (DLS) and cryogenic transmission electron microscopy (Cryo-TEM) measurements. The pH titration results show that CGS12 exhibits anionic surfactant properties and CAPB exists as a zwitterionic form at pH 7.0. The surface tension results show that the critical micelle concentration (CMC) values of the CAPB/CGS12 mixture are low, and basically exhibit a decreasing trend with decreasing molar ratio of CAPB (XCAPB). The variation of the CMC of the mixture reveals that the mixing is close to ideal. The DLS results indicate that the CAPB/ CGS12 mixture mainly forms the larger aggregates with the hydrate radii approximately 70-145 nm at various XCAPB. The Cryo-TEM images further demonstrate the CAPB/CGS12 mixtures mainly form vesicles. The results indicate that the aggregate size and microstructure of the mixture change little with the variation of XCAPB.

Zinc(II) Complexes Derived from Schiff Bases: Syntheses, Structures, and Biological Activity

Three new zinc(II) complexes, [Zn2I2(L1)2] (1), [Zn(HL2)2(NCS)2] (2), and [ZnIL3] (3), where L1 is the anionic form of 2-[(6-methylpyridin-2-ylimino)methyl]phenol (HL1), HL2 is the zwitterionic form of 2-(cyclopropyliminomethyl)-5-fluorophenol (HL2), and L3 is the anionic form of 5-bromo-2-[(3-morpholin-4-ylpropylimino)methyl] phenol (HL3), have been prepared and characterized by elemental analyses, IR, UV and NMR spectra, and single crystal X-ray crystallographic determination. Complex 1 is a dinuclear zinc complex, and complexes 2 and 3 are mononuclear zinc complexes. The Zn atoms in the complexes are in tetrahedral coordination. The effect of the complexes on the antimicrobial activity against Staphylococcus aureus, Escherichia coli, and Candida albicans were evaluated.

Synthesis, structure and biological activity of four new picolinohydrazonamide derivatives

Four new picolinohydrazonamide derivatives, namely, 6-methyl-N′-(morpholine-4-carbonothioyl)picolinohydrazonamide, C12H17N5OS, 6-chloro-N′-(morpholine-4-carbonothioyl)picolinohydrazonamide methanol monosolvate, C11H14ClN5OS·CH3OH, 6-chloro-N′-(4-phenylpiperazine-1-carbonothioyl)picolinohydrazonamide, C17H19ClN6S, and 6-chloropicolinohydrazonamide, C6H7ClN4, have been synthesized and characterized by NMR spectroscopy and single-crystal low-temperature X-ray diffraction. In addition, their antibacterial and anti-yeast activities have been determined. The first three compounds adopt the zwitterionic form in the crystal structure regardless of the presence or absence of solvent molecules in the structure. They also adopt the same symmetry, i.e. P21/c (P21/n), unlike the fourth structure which is chiral and has the space group P212121. For all the studied cases, intermolecular N—H...O and N—H...N hydrogen bonds play an essential role in the formation of the structures.

Complexation of 5-aminovaleric acid zwitterions in aqueous/methanol solution by heterotopic tri-cationic receptors

Heterotopic tri-cationic receptor based on 4,10,16-triaza-18-crown-6 is capable of efficient and selective binding of the zwitterionic form of 5-aminovaleric acid (5-AVA) in aqueous/methanol solution.