The cationic tetranuclear cobalt complex of the geometry Cl-CoL-Cl-CoL-Cl-CoL-Cl-CoL (where L is 6,6 000 -dimethyl-2,2 0 :6 0 ,2 00 :6 00 ,2 000 -quaterpyridine) has been synthesized and structurally characterized. The structural unit contains one cationic ligand, two Eu(NO 3 ) 5 dianions, two solvent acetonitrile molecules and some disordered water molecules. The salt crystallizes in the monoclinic space group C2/c with a = 17.405 (3) Å , b = 28.700 (5) Å and c = 23.350 (5) Å , b = 95.14 (2)8. The cation is C 2 -symmetrical, the central Cl atom lies on the twofold axis. This structure is another example of centro-noncentro ambiguity: in the centrosymmetric model, the terminal Cl in the cation is disordered between the two ends of the chain. The Eu ion is coordinated by five nitro groups, the coordination number is 10-two oxygen atoms of every nitro group are involved in the coordination with the mean Eu-O distance of 2.52(3) Å . The quaterpyridine ligands are folded, the dihedral angle between the terminal ring planes is 29.3 (2) and 32.8 (3)8 in the two symmetry independent ligands. In the crystal structure the coulombic attraction between the cations and anions seems to be a driving force; the ionic species make a chessboard-like pattern, the voids in such created structure are filled with the solvent-acetonitrile molecules as well as by some disordered waters.Keywords Co complexes Á Eu complexes Á Centro-noncentro ambiguity Á Crystal packing
Results and DiscussionThe use of transition metal ions capable of bridging multidentate ligands to construct pre-programed, self-assembled small inorganic systems and multi-dimensional infinite supramolecular networks is an area of chemistry which has received ever-increasing attention over recent years. Up to date, many fascinating supramolecular structures have been obtained by using metal ions and ligands containing nitrogen-donor atoms, for instance bipyridine [1], terpyridine [2] or tetrapyridine [3], to name a few.In the present work, we extend these studies of the metalo-ligand complexes based on tetrapyridine ligand coordinated with d-and f-metal ions, obtained in one-pot reaction. The crystals contain cation with four organic ligands coordinated to the four cobalt ion bridged by chloride ions and two penta-nitrato anionic species with nitrate oxygen atoms coordinated to trivalent europium ion. The formation of this type of complex may be understood considering the large stability of polynitrato counter ions [4]. The high affinity of the europium ions for nitrato anions does not allow heterometallic Co-Eu complexes to be prepared from N 4 -donor ligand if the latter anions are present in solution [5].The investigated complex may be of use in several fields of coordination chemistry. In particular, d-and f-polynuclear complexes might be used to fabricate nanomagnetic materials of the potential use in many fields, [6] and due to their electronic properties such as high conductivity as molecular devices in the field of nano-electronics [7,8]. Figures 1 and ...