چکیده
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Hydrazones are an important class of Schiff bases that are considered as one of the most
extensively utilized ligands for the development of coordination chemistry of transition
metals. This matter is related to their easy way of preparation, structural divergence, and
solubility in commonly available solvents [1-3]. These are illustrious from the other members
of the same class due to the existence of interlinked nitrogen atoms (-C(O)-NH-N=CH-) and
can coordinate with the metal atoms in both neutral and deprotonated forms [4].
Picolinohydrazide, by having a pyridine ring connected to the hydrazone unit is one of the
attractive compound for preparing diatopic Schiff base ligands. In this research, we report the
synthesis, characterization and Hirschfield surface analysis of Zn(II) complexes with (E)-N'-
(1-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl) ethylidene) picolinohydrazide. Tetranuclear
zinc complex was synthezied in methanol solvent and its crystals were obtained by slow
sovlent evaporating method. The obtained complex was characterized by spectroscopic
methods and single crystal X-ray analysis which revealed it is a tetranuclear acetato-bridged
Zn(II) complex and the picolinohydrazone ligand act as both bridging and chelating ligand.
This copmpound is crystallized in monoclinic system and there are strong intermolecular
interactions. The zinc ions are five coordinated and the acetato ligands act as briding group
between metal cores. Intermolecular interactions in this compound were studied by Hirschfeld
surface analysis. This analysis indicated there are strong C–H···O. O–H···O and O–H···N
interactions in the crystal structur of the Zn(II) cluster.
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