Journal of the Chemical Society Dalton Transactions · 1983 · 62 citations · 0 references
Natural SciencesBiochemistryChemistryCrystal StructureInorganic ChemistrySolid-state ChemistryCoordination ChemistryCrystal ChemistryCrystal SystemsMetal-ligand BondingTransition Metal ChemistryTransition Metal ComplexesComplexation ChemistryManganese ChelationMetalloid Coordination ChemistrySpectroscopic CharacterizationSpectroscopic Characterization Of Metal-ligand BondsUnit Cell DeterminationX-ray Diffraction AnalysisX-ray Structure Determination
The chelating behaviour of neutral and deprotonated 2,6-diacetylpyridine bis(benzoylhydrazone)(H2dapb) has been investigated in some new complexes of MnII, CoII, NiII, CuII, and ZnII. An X-ray diffraction analysis was carried out on [Mn(H2dapb)(OH2)Cl]Cl. The crystals are monoclinic, space group P21/c, with unit-cell dimensions a= 7.065(6), b=17.096(9), c=19.446(13)Å, β= 96.89(8)°, and Z= 4. The structure was solved by the heavy-atom technique from 1 545 observed independent reflections recorded at room temperature on an automated diffractometer and refined to a final R value of 0.0329. The structure consists of [Mn(H2dapb)(OH2)Cl]+ cations and Cl– anions. The cation has a pentagonal-bipyramidal geometry, with H2dapb forming the equatorial plane and the H2O and Cl groups occupying the axial positions. The i.r. spectra suggest differences in the interaction of these metals with the hydrazone molecule.