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A Molecular Chain of Four CoII Ions Stabilized by a Tris-Pyridyl/Bis-β-Diketonate Ligand
Leoní A.
Barrios A,
David
Aguilà A,
Olivier
Roubeau B,
Keith S.
Murray C,
Guillem
Aromí A D
A
Departament de Química Inorgànica, Universitat de Barcelona, Diagonal 647, 08028 Barcelona, Spain.
B
Instituto de Ciencia de Materiales de Aragón, CSIC and Universidad de Zaragoza, Plaza San Francisco s/n, 50009 Zaragoza, Spain.
C
School of Chemistry, Building 23, Monash University, Clayton, Vic. 3800, Australia.
D
Corresponding author. Email: guillem.aromi@qi.ub.es
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Australian Journal of Chemistry 62(9) 1130–1136 http://dx.doi.org/10.1071/CH09183
Submitted: 1 April 2009
Accepted: 25 April 2009
Published online: 17 September 2009
Abstract
The synthesis and characterization of a tris-pyridyl/bis-β-diketone molecule (H2L) is reported. This compound acts as a hexadentate ligand towards CoII to facilitate the assembly of a tetranuclear molecular chain of closely spaced metals with formula [Co4L2(MeOH)8](NO3)4 (1), which exhibits a very flat [Co4L2]4+ platform, as determined by single-crystal X-ray diffraction crystallography. Complex 1 readily exchanges axial methanol ligands with water molecules. The bulk magnetization of the resulting hydrate, 1a, shows that the metals in the [Co4L2]4+ moiety exhibit spin-orbit coupling and antiferromagnetic exchange interactions.
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