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The title complex, [Cu2(C10H4N4)(C41H39P3)2](BF4)2·CH2Cl2, was synthesized and characterized. Two copper(I) ions are bridged by 4,4′-di-4-pyridyl­diazene (more commonly as 4,4′-azobi­pyridine). The discrete dinuclear cation contains two distorted tetrahedral copper(I) centers. Each CuI atom is coordinated by one 1,1,1-tris­(di­phenyl­phosphino­methyl)­ethane mol­ecule and one 4,4′-azobi­pyridine ligand. The complex sits on a center of symmetry; the solvent molecule is disordered across another center of symmetry. On irradiation of the copper(I) complex in di­chloro­methane at 365 nm, the trans/cis ratio of the complex is reversed.

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The title compound, C18H17N3O2·CH4O, is a Schiff base compound, which is derived from the condensation of equimolar amounts of 4-amino­antipyrine and 4-hydroxy­benzaldehyde. In the crystal structure, the MeOH molecules are linked to the Schiff base molecules through intermolecular O—H...O hydrogen bonds.

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The title compound, C20H19N3O, is a Schiff base compound derived from 4-amino­antipyrine and cinnam­aldehyde. As expected, the molecular structure adopts a trans configuration about the central C=N double bond.

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The title compound, C17H12ClNO, is a Schiff base compound derived from the condensation of equimolar quantities of 5-chloro­salicyl­aldehyde and 1-naphthyl­amine. The structure displays a trans configuration with respect to the imine C=N double bond. The N atom is also involved in an intramolecular O—H...N hydrogen bond. In the crystal structure, the mol­ecules stack along the b axis.

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In the mononuclear title compound, [Zn(C13H15ClNO)2], the ZnII atom is four-coordinated by two N atoms and two O atoms from two Schiff base ligands in a slightly distorted tetra­hedral geometry.

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In the mononuclear title compound, [Co(C13H15ClNO)2], the Co atom is four-coordinated by two N atoms and two O atoms from two Schiff base ligands in a slightly distorted tetra­hedral geometry.
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