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Dinuclear terephthalato-bridged nickel(II) complexes. Structural characterization and magnetic properties |
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| Authors: | Salah S Massoud Franz A Mautner |
| Institution: | a Department of Chemistry, University of Louisiana at Lafayette, P.O. Box 44370 Lafayette, LA, USA b Institut für Physikalische and Theoretische Chemie, Technische Universität Graz, A-8010 Graz, Austria c Departament de Quimica Inorganica, Universitat de Barcelona, Diagonal 647, 08028 Barcelona, Spain |
| Abstract: | The dinuclear terephthalato-bridged nickel(II) complexes Ni2(cyclen)2(μ-tp)](ClO4)2 (1) Ni2(trpn)2(μ-tp)(H2O)2](ClO4)2 (2) and Ni2(3,3,3-tet)2(μ-tp)(H2O)2](ClO4)2 · 2H2O (3), where tp = terephthalate dianion, cyclen = 1,4,7,10-tetraazacyclododecane, trpn = tris(3-aminopropyl)amine and 3,3,3-tet = 1,5,9,13-tetraazatridecane, were synthesized and structurally characterized by X-ray crystallography. Their magnetic susceptibilities were also determined at variable temperatures over the range 2-300 K. The structures of these complexes consist of μ-tp bridging two Ni(II) centers in a bis(bidentate) bonding fashion in 1 and in bis(monodentate) bonding fashion in 2 and 3. The coordination geometry around the Ni(II) ions in these compounds has a distorted octahedral geometry with four nitrogen atoms from the amine ligand (cyclen, trpn or 3,3,3-tet) and two coordinated oxygen atoms supplied by the chelated carboxylate group of the bridged terephthalate ligand in 1, and by one tp-carboxylate-oxygen in 2 and 3. The sixth coordination site in the last two complexes 2 and 3 is achieved via an oxygen atom from a coordinated water molecule. The intradimer Ni…Ni distances in these complexes are 10.740, 11.428 and 11.537 Å for 1, 2 and 3, respectively. The electronic spectra of the complexes in aqueous solutions are in complete agreement with the assigned X-ray geometry around the Ni(II) centers. Also, the analysis of the infrared spectral data for the ν(COO−) stretching frequencies of the tp-carboxalato groups reveals the existence of the bis(bidentate) and bis(monodentate) coordination modes for the bridged terephthalate ligand in 1, 2 and 3, respectively. Despite the different coordination modes of the tp bridging ligand in these complexes, they all exhibit very weak antiferromagnetic coupling. The coupling constants J were found to be −2.2, −0.6 and −1.5 cm3 K mol−1 for the complexes 1, 2 and 3, respectively. The structural and magnetic results of 1-3 are discussed in relation to the other related published μ-terephthalato dinuclear Ni(II) compounds. |
| Keywords: | Nickel(II) complexes Dinuclear complexes Terephthalato bridged Crystal structure Magnetic properties |
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