Nd(III)和Pr(III)与三齿席夫碱配体N' -(1 -(吡啶- 2 -基)乙基)烟酰肼配合物的合成、表征和单晶x射线晶体学

M. Faye, Papa Aly Gaye, M. Sow, M. Dieng, F. Tamboura, N. Gruber, M. Gaye
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引用次数: 2

摘要

N′-(1 -(吡啶- 2 -基)乙基)烟酰肼(HL)在镧系元素(III)化学中的应用产生了一个单核和一个双核配合物。在甲醇中以1:1的Nd(NO3)3.6H2O或Pr(CH3COO)3.6H2O/HL得到配合物[Nd (HL)2(NO3)2(H2O)2]、(NO3)(1)和{[Pr(L)(h2 - oocch3)(H2O)](h1:h2: m-OOCCH3)2[Pr (L)(h2 - oocch3)(H2O)]}(2)。用x射线单晶晶体学对配合物结构进行了解析。在单核配合物中,Nd3+原子由两个中性配体分子以三齿作用方式配位,两个硝酸盐阴离子以双齿作用方式配位,两个配位水分子产生十二配位Nd原子。在配合物(2)中,Pr3+原子由两个醋酸盐阴离子双桥接,每个金属离子由一个三齿单去质子分子配体、一个双齿醋酸基团和一个配位水分子配位。每一个Pr3+原子都是九配位的,其环境最好被描述为三叠棱镜几何。配合物1在单斜空间群C2/c中结晶,参数为:a = 22.7657(8) Å, b = 8.4276(3) Å, c = 18.0831(7) Å, b = 114.851(2)°,V = 3148.2(2) Å3, Z = 4, R1 = 0.032, wR2 = 0.098。配合物2在单斜空间群P21/n中结晶,参数为:a = 11.5388(6) Å, b = 14.1087(8) Å, c = 12.2833(6) Å, b = 102.211(2)°,V = 1954.45(18) Å3, Z = 2, R1 = 0.029, wR2 = 0.066。超分子结构由多个氢键巩固。
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Synthesis, Characterization and Single Crystal X–ray Crystallography of Nd(III) and Pr(III) Complexes with the Tridentate Schiff Base Ligand N'–(1–(pyridin–2–yl)ethylidene)nicotinohydrazide
The use of N'–(1–(pyridin–2–yl)ethylidene)nicotinohydrazide (HL) in lanthanide(III) chemistry has yielded one mononuclear and one dinuclear complexes. The 1:1 Nd(NO3)3.6H2O or Pr(CH3COO)3.6H2O/HL in methanol afforded the complexes [Nd (HL)2(NO3)2(H2O)2].(NO3) (1) and {[Pr(L)(h2–OOCCH3)(H2O)](h1:h2:m–OOCCH3)2[Pr (L)(h2–OOCCH3)(H2O)]} (2). The structures of the complexes were solved by single crystal X–ray crystallography. In the mononuclear complex, the Nd3+ atom is coordinated by two neutral molecules of ligand acting in tridentate fashion, two nitrate anions acting in bidentate manner and two coordinated water molecules yielding a twelve–coordinated Nd atom. In the complex (2) the Pr3+ atoms are doubly bridged by two acetates anions and each metal ion is coordinated by one tridentate monodeprotonated molecule ligand, one bidentate acetate group and one coordinated water molecule. Each Pr3+ atom is nine–coordinated with an environment best described as a tricapped prismatic geometry. Complex 1 crystallizes in the monoclinic space group C2/c with the following parameters: a = 22.7657(8) Å, b = 8.4276(3) Å, c = 18.0831(7) Å, b = 114.851(2)°, V = 3148.2(2) Å3, Z = 4, R1 = 0.032, wR2 = 0.098. Complex 2 crystallizes in the monoclinic space group P21/n with the following parameters: a = 11.5388(6) Å, b = 14.1087(8) Å, c = 12.2833(6) Å, b = 102.211(2)°, V = 1954.45(18) Å3, Z = 2, R1 = 0.029, wR2 = 0.066. The supramolecular structures are consolidated by multiple hydrogen bonds.
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