Angular trinuclear copper(II) complexes of N4O-donor ligand: Syntheses, crystal structures and magnetic properties

作者：Das Oindrila; Zangrando Ennio; Paine Tapan Kanti^*

来源：Inorganica Chimica Acta, 2009, 362(10): 3617-3623.

DOI：10.1016/j.ica.2009.04.006

• Copper
• Trinuclear complexes
• Schiff-base
• Solid-state structures
• Hydrogen bonds
• Antiferromagnetic coupling

Two trinuclear copper(II) complexes of a Schiff-base type N4O-donor ligand (LH) derived from 4,4,9,9-tetramethyl-5,8-diazadodecane-2,11-dione and 1,3-diaminopropan-2-ol are reported. Complex [Cu3L2 (ClO4)(4)] (1) has an angular C-2-symmetric trinuclear core as revealed from single-crystal X-ray diffraction studies. The terminal coppers are in square-pyramidal geometry with an N3O2 coordination environment while the central one is in octahedral geometry with an N2O4 donor environment. Complex [Cu3L2 (ClO4)(N-3)(H2O)](ClO4)(2) center dot H2O (2) has an unsymmetrical trinuclear core with an intramolecular hydrogen bonding interaction between the water and azide anion coordinated to Cu(1) and Cu(3) center, respectively. All the copper centers in 2 are in square-pyramidal geometry. The average Cu center dot center dot center dot Cu distance between closest metal ions in both the complexes is 3.897 angstrom. The coordination environment of coppers in 1 approximately mimics that of multicopper oxidases in the oxidized form and the environment in 2 mimics that of the azide derivative of ascorbate oxidase. Both 1 and 2 exhibit doublet spin ground state due to strong antiferromagnetic coupling operating through the alkoxo-bridged oxygen atoms between the copper centers.

• 出版日期2009-8-1