Muñoz Juan Carlos, Atria Ana María, Garland Maria Teresa, Baggio Ricardo
Instituto de Química, Facultad de Ciencias Exactas y Naturales, Universidad de Antioquia, Medellín, Colombia.
Acta Crystallogr C. 2009 Mar;65(Pt 3):m121-7. doi: 10.1107/S0108270109002534. Epub 2009 Feb 13.
The structures of three new polymeric lanthanide complexes, poly[[bis(2,2'-bipyridine)-mu(4)-itaconato-di-mu(3)-itaconato-digadolinium(III)] tetrahydrate], {[Gd(2)(C(5)H(4)O(4))(3)(C(10)H(8)N(2))(2)].4H(2)O}(n), (I), poly[diaqua(2,2'-bipyridine)di-mu(3)-itaconato-mu(2)-itaconato-digadolinium(III)], Gd(2)(C(5)H(4)O(4))(3)(C(10)H(8)N(2))(H(2)O)(2), (II), and poly[[bis(2,2'-bipyridine)-mu(4)-itaconato-di-mu(3)-itaconato-diholmium(III)] dihydrate], {[Ho(2)(C(5)H(4)O(4))(3)(C(10)H(8)N(2))(2)].2H(2)O}(n), (III), have been solved from twinned specimens. Compound (I) presents a two-dimensional polymeric structure parallel to (011) built up around two independent nine-coordinated Gd centres displaying similar GdO(7)N(2) environments, with both N-donor atoms in each provided by a chelating 2,2'-bipyridine (bpy) unit. The coordinating O atoms are from three different itaconate (ita) anions (itaconic acid is 2-methylidenebutanedioic acid). Compound (II) also presents two independent Gd centres (one ten- and the other eight-coordinated), but the overall formula and individual coordinations are different from those of (I). The chemical unit is in this case completed by one bpy ligand, three ita anions (one of them displaying a new, hitherto unreported, mu(3)-O,O':O',O'':O''' binding mode) and two aqua ligands. The whole structure is built up around a twofold rotation axis passing through both cations, as well as through the centre of the bpy ligand and one of the ita anions, thus making only half of the chemical unit independent. Finally, compound (III) presents a single independent Ho centre, a bpy unit and one and a half ita anions (one of them bisected by a twofold rotation axis) in the asymmetric unit, plus two (disordered) nonbonded solvent water molecules. In compounds (II) and (III), those ita anions bisected by a symmetry element incompatible with the internal symmetry of the ligand exhibit disorder in the C=CH(2) group.
三种新型聚合物镧系配合物,聚[[双(2,2'-联吡啶)-μ(4)-衣康酸根-二-μ(3)-衣康酸根-二钆(III)]四水合物],{[Gd₂(C₅H₄O₄)₃(C₁₀H₈N₂)₂]·4H₂O}ₙ,(I);聚[二水合(2,2'-联吡啶)-二-μ(3)-衣康酸根-μ(2)-衣康酸根-二钆(III)],[Gd₂(C₅H₄O₄)₃(C₁₀H₈N₂)(H₂O)₂]ₙ,(II);以及聚[[双(2,2'-联吡啶)-μ(4)-衣康酸根-二-μ(3)-衣康酸根-二钬(III)]二水合物],{[Ho₂(C₅H₄O₄)₃(C₁₀H₈N₂)₂]·2H₂O}ₙ,(III)的结构已从孪晶标本中解析出来。化合物(I)呈现出一个平行于(011)的二维聚合物结构,围绕两个独立的九配位钆中心构建,显示出相似的GdO₇N₂环境,每个中心的两个氮供体原子均由一个螯合的2,2'-联吡啶(bpy)单元提供。配位的氧原子来自三种不同的衣康酸根(ita)阴离子(衣康酸为2-亚甲基丁二酸)。化合物(II)也有两个独立的钆中心(一个十配位,另一个八配位),但其总体化学式和单个配位情况与化合物(I)不同。在这种情况下,化学单元由一个bpy配体、三个ita阴离子(其中一个呈现一种新的、迄今未报道的μ(3)-O,O':O',O'':O'''键合模式)和两个水合配体完成。整个结构围绕一个通过两个阳离子以及bpy配体中心和一个ita阴离子中心的二次旋转轴构建,因此只有一半的化学单元是独立的。最后,化合物(III)在不对称单元中呈现一个单一独立的钬中心、一个bpy单元和一个半ita阴离子(其中一个被二次旋转轴平分),外加两个(无序的)非键合溶剂水分子。在化合物(II)和(III)中,那些被与配体内在对称性不相容的对称元素平分的ita阴离子在C=CH₂基团中表现出无序。