The asymmetric unit of the 1:19 title co-crystal of 2-amino-4-(3,4-dimeth-oxy-phen-yl)-5,6-dihydro-benzo[h]quinoline-3-carbo-nitrile and 3-amino-1-(3,4-dimeth-oxy-phen-yl)-9,10-dihydro-phenanthrene-2,4-dicarbonitrile, 0.05C(22)H(19)N(3)O(2)·0.95C(24)H(19)N(3)O(2), has the atoms of the fused-ring system and those of the amino, cyano and dimeth-oxy-phenyl substitutents overlapped. The fused-ring system is buckled owing to the ethyl-ene linkage in the central ring with the two flanking aromatic rings being twisted by 31.9 (1)°. The ring of the dimeth-oxy-phenyl substituent is twisted by 72.4 (1)° relative to the amino- and cyano-bearing aromatic ring. In the crystal, mol-ecules are linked by duplex amine N-H⋯O(meth-oxy) hydrogen bonds in a cyclic association [graph-set R(2) (2)(7)], generating a helical chain structure extending along [201].
In the current work, we have examined the interaction activities of Pluronic F-68 with cationic conventional, cetyltrimethylammonium bromide (CTAB), and gemini surfactant, pentanediyl-1, 5-bis(dimethylcetylammonium bromide), (16-5-16) by means of surface tension and conductivity measurements. The critical micelle concentration (cmc) values of pure 16-5-16 and CTAB have been evaluated tensiometrically and conductometrically, while the cmc values of pure F-68 and binary mixtures were determined only from the surface tension plots. Various interfacial and micellar parameters including surface excess concentration (Γmax), minimum area per molecule (Amin), surface pressure at cmc (πcmc), packing parameter (p), and interaction parameter (β) have been estimated and discussed in detail. Various thermodynamic parameters including Gibbs free energy of micellization (), standard free energy of adsorption at the air–water interface (), excess free energy of micellization (ΔGex), and molar free energy at the maximum adsorption achieved at cmc (Gmin) have been calculated.
We have investigated the antibacterial activity of some new steroidal thiosemicarbazones and their Pd(II) metal complexes were prepared by the reaction of the thiosemicarbazones with [Pd(DMSO)(2)Cl(2)]. The steroidal thiosemicarbazones were prepared by the reaction of thiosemicarbazides with a steroidal ketone. The structures of these compounds were elucidated by IR, (1)H-NMR, (13)C-NMR, FAB mass spectroscopic methods, elemental analyses and TGA analysis. The antibacterial activity of these compounds were tested in vitro by the disk diffusion assay against two Gram-positive and two Gram-negative bacteria. The results showed that steroidal complexes are better inhibitors of both types of the bacteria (Gram-positive and Gram-negative) as compared to steroidal thiosemicarbazones. Compound Ia displays remarkable antibacterial activity as compared to amoxicillin.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.