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Dalton Transactions

The international journal for inorganic, organometallic and bioinorganic chemistry




Paper

Dalton Trans., 2007, 5140 - 5147, DOI: 10.1039/b711655a


Metamorphosis of a butterfly: synthesis, structural, thermal, magnetic and DFT characterisation of a ferromagnetically coupled tetranuclear copper(II) complex

Robert P. Doyle, Thomas Bauer, Miguel Julve, Francesc Lloret, Joan Cano, Mark Nieuwenhuyzen and Paul E. Kruger


The reaction in water of Cu(OH)2 with 2,2-bipyridine (bipy) and (NH4)2HPO4 in a 4 : 4 : 2 molar ratio under an inert atmosphere leads to the formation of a tetranuclear copper(II) complex of formula {[(H2O)2Cu4(bipy)44–PO4)22–OH)]·0.5HPO4·15.5H2O}, 1, with butterfly topology. The structure of the tetranuclear core in 1 consists of four crystallographically unique copper(II) ions in approximate square-pyramidal geometry with each coordinated to a bipy ligand and interacting through two µ4–O,O,O-phosphate bridges. Additional bridging between Cu(3) and Cu(4) is provided by a hydroxide ligand, whereas two water molecules cap the Cu(1) and Cu(2) square pyramids to yield a N2O3 chromophore at each copper atom. Adjacent tetranuclear units align in anti-parallel fashion where proximate metal-bound water molecules interact with each other through both intra- and inter-molecular H-bonding to link two such clusters. These pairs then further associate through interactions between bipy ligands to form a 2D sheet with neighbouring sheets separated by H-bonded lattice water molecules, which form a 2D H-bonded network. Variable-temperature magnetic susceptibility measurements performed upon 1 reveal net intramolecular ferromagnetic coupling between the copper(II) ions and this is supported and rationalized by a DFT study.

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