Abstract

The title compound, [PdCl2(C28H24N2)]·CH3OH, was pre­pared from the reaction of PdCl2(DMSO)2 (DMSO is di­methyl sulfoxide) and N,N′-bis­(4-methyl­phen­yl)-1,2-di­phenyl­ethane-1,2-di­imine in methanol. The chelating di­imine core of the title compound deviates slightly from planarity, with an N—C—C—N torsion angle of 5.3 (3)°. Delocalization in the di­imine core is indicated by N—C and C—C bonds that are, respectively, longer and shorter than those found in related nonchelating di­imines. The distorted square-planar coordination environment around the PdII atom is manifested as bond angles that are smaller and larger than 90°, and palladacycle torsion angles of −173.22 (16) and 167.06 (16)°. These deviations are attributed to the small bite angle of 79.13 (8)° of the di­imine chelate. The crystal packing exhibits weak inter­molecular hydrogen-bonding inter­actions involving aromatic H atoms, Cl atoms and inter­calated methanol solvent mol­ecules, defining layers parallel to (010).

Highlights

  • The title compound, [PdCl2(C28H24N2)]CH3OH, was prepared from the reaction of PdCl2(DMSO)2 (DMSO is dimethyl sulfoxide) and N,N0 -bis(4-methylphenyl)-1,2-diphenylethane1,2-diimine in methanol

  • Delocalization in the diimine core is indicated by N—C and C—C bonds that are, respectively, longer and shorter than those found in related nonchelating diimines

  • The distorted square-planar coordination environment around the PdII atom is manifested as bond angles that are smaller and larger than 90, and palladacycle torsion angles of 173.22 (16) and 167.06 (16)

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Summary

Data collection

The title compound, [PdCl2(C28H24N2)]CH3OH, was prepared from the reaction of PdCl2(DMSO) (DMSO is dimethyl sulfoxide) and N,N0 -bis(4-methylphenyl)-1,2-diphenylethane1,2-diimine in methanol. The chelating diimine core of the title compound deviates slightly from planarity, with an N—C—. Delocalization in the diimine core is indicated by N—C and C—C bonds that are, respectively, longer and shorter than those found in related nonchelating diimines. The distorted square-planar coordination environment around the PdII atom is manifested as bond angles that are smaller and larger than 90 , and palladacycle torsion angles of 173.22 (16) and 167.06 (16). These deviations are attributed to the small bite angle of 79.13 (8).

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Refinement

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