Citation: YOU Xiu-Li, HU Tao, XU Lai, WENG Ying, XIA Hong-Ying. Syntheses, Crystal Structure and Magnetism of a Hexanuclear Copper(Ⅱ) Cluster with the Unique Two-parallel Three-site Strings Configuration[J]. Chinese Journal of Structural Chemistry, ;2015, 34(4): 569-575. doi: 10.14102/j.cnki.0254-5861.2011-0567
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Treatment of a heptadentate ligand 2,2'-(((pyridine-2,6-diyl-bis(methylene))-bis((pyridin-2-ylmethyl)azanediyl))bis(methylene))diphenol (H2L) possessing pyridinyl and phenolate groups, with three equivalents of Cu(ClO4)2·6H2O in methanol under base conditions, gave rise to a hexanuclear cluster complex [Cu6L2(OH)4](ClO4)4·4MeCN·0.5MeOH (1). Complex 1 crystallizes in triclinic, space group P1 with a=12.068(12), b=12.567(12), c=16.279(16)Å, α=105.694(12), β=93.631(13), γ=112.017(11)°, V=2166(4)Å3, Z=1, μ=1.651 mm-1, Dc=1.599 Mg/m3, T=296(2) K, C74.5H79.5N14O24.5Cl4Cu6, Mr=2086.12, F(000)=1062.5, S=1.061, R=0.0521 and wR=0.1270. In the cation of complex 1, the six copper cores are arranged into a two-parallel three-site strings configuration with each metal exhibits a slightly distorted square-pyramidal geometry, resulting from the connection of donor pyridinyl nitrogen and phenolate oxygen atoms in ligand H2L, and/or the oxygen donors in hydroxyl groups. In addition, magnetic susceptibility measurements revealed complex 1 displayed antiferromagnetic coupling.
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