Synthesis, structures and magnetochemistry of binuclear cobalt(II), nickel(II) and copper(II) complexes of 2,6-diformyl-4-methylphenol dioxime

Citation
D. Black et al., Synthesis, structures and magnetochemistry of binuclear cobalt(II), nickel(II) and copper(II) complexes of 2,6-diformyl-4-methylphenol dioxime, J CHEM S DA, (23), 1998, pp. 3953-3960
Citations number
41
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS
ISSN journal
03009246 → ACNP
Issue
23
Year of publication
1998
Pages
3953 - 3960
Database
ISI
SICI code
0300-9246(199812):23<3953:SSAMOB>2.0.ZU;2-H
Abstract
Reaction of 2,6-diformyl- and 2,6-diacetyl-4-methylphenol with a large exce ss of both NH2OH . HCl and CH3CO2K in EtOH affords high yields of 2,6-difor myl-4-methylphenol dioxime (2-hydroxy-5-methylbenzenedicarbaldehyde dioxime ) (H3L1) and 2,6-diacetyl-4-methylphenol dioxime (H3L2), respectively. The crystal structure of (H3L2) shows intramolecular hydrogen bonding with long -range intermolecular pi-stacking interactions and an extended intermolecul ar hydrogen-bonding network. The binuclear complexes of Co-II, Ni-II and Cu -II-[Co-2(H2L1)(2)(MeOH)(2)(H2O)(2)]Cl-2. 2MeOH, [Ni-2(H2L1)(2)(H2O)(4)][Cl O4](2). 2H(2)O and [Cu-2(H2L1)(2)(ClO4)(2)] respectively-derived from the d ioxime ligand (H3L1) have been synthesized and characterised and their sing le-crystal structures determined. The structure of [Co-2(H2L1)(2)(MeOH)(2)( H2O)(2)](2+) shows each high-spin Co-II to be six-co-ordinate and bound to an N2O4-donor array presented by two dioxime ligands and axially co-ordinat ed H2O and MeOH molecules, the dioxime ligands co-ordinating via the imino N- and phenoxy O-donors. The structure of [Ni-2(H2L1)(2)(H2O)(4)](2+) shows two octahedrally co-ordinated Ni-II each with an N2O4 donor set similar to that in [Co-2(H2L1)(2)(MeOH)(2)(H2O)(2)](2+) except that the co-ordination sphere of each Ni-II is completed by axial ligation to two H2O molecules. The structure of [Cu-2(H2L1)(2)(ClO4)(2)] confirms N2O4 donation at CUII Wi th two bidentate ClO4- anions, Cu ... O 2.51(2), 2.76(2) Angstrom, interact ing with the metal centres on either side of the planar oxime-phenolate arr ay. In all three complexes the two dioxime ligands are monodeprotonated at the phenolic oxygen, and the oximes are linked by hydrogen bonds, which res ults in a pseudo-macrocyclic framework. Magnetic susceptibility measurement s on the complexes over the range 2.5-340 K confirm that the complexes are antiferromagnetically coupled with values for the magnetic exchange constan t J of -6.9 +/- 0.1, -16.0 +/- 0.6, and -452 +/- 4 cm(-1) for [Co-2(H2L1)(2 )(MeOH)(2)(H2O)(2)]Cl-2, [Ni-2(H2L1)(2)(H2O)(4)][ClO4](2) and [Cu-2(H2L1)(2 )(ClO4)(2)] respectively.