A new tetranuclear complex of zinc(II) with P.P'-diphenylmethylenediphosphinate and 2,2'-bipyridine ligands was synthesized. [(pcp)(2,2'-bipy)Zn (mu(3)-pcp)Zn (2,2'-bipy)](2) center dot 6H(2)O was characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis and X-ray diffractometry. The structure consists of tetranuclear complexes connected through water hydrogen-bonding interactions in corrugated 2D layers. Two crystallographically independent zinc ions are in a distorted five-coordinate environment, being surrounded by three oxygen atoms of phosphinate groups (from two pep ligands) and by two bipy nitrogen donors. Of the two independent pep anions the first one utilizes all of its oxygen donors to coordinate one metal as bidentate and two metal atoms as a monodentate ligand, whereas the second one is only bidentate for one metal atom.
Synthesis and Structural Characterization of a Tetranuclear Zinc(II) Complex with P,P-Diphenylmethylenediphosphinate (pcp) and 2,2-Bipyridine (2,2-bipy) Ligands
Ienco Andrea;Midollini Stefano;
2007
Abstract
A new tetranuclear complex of zinc(II) with P.P'-diphenylmethylenediphosphinate and 2,2'-bipyridine ligands was synthesized. [(pcp)(2,2'-bipy)Zn (mu(3)-pcp)Zn (2,2'-bipy)](2) center dot 6H(2)O was characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis and X-ray diffractometry. The structure consists of tetranuclear complexes connected through water hydrogen-bonding interactions in corrugated 2D layers. Two crystallographically independent zinc ions are in a distorted five-coordinate environment, being surrounded by three oxygen atoms of phosphinate groups (from two pep ligands) and by two bipy nitrogen donors. Of the two independent pep anions the first one utilizes all of its oxygen donors to coordinate one metal as bidentate and two metal atoms as a monodentate ligand, whereas the second one is only bidentate for one metal atom.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.