MIXED-LIGAND GERMANIUM–LANTHANIDE COMPLEXES WITH 1-HYDROXYETHYLIDENEDIPHOSPHONIC ACID AND 2,2’-BIPYRIDINE

E. Martsinko, I. Seifullina, E. Chebanenko, A. G. Pesaroglo
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Abstract

There were developed the novel methods for the synthesis of six mixed- metal and mixed-ligand complexes of germanium and rare earth metals (Pr, Nd, Dy, Ho, Tm, Lu) with 1-hydroxyethylidenediphosphonic acid and 2,2´-bipyridine. The compounds have been characterized using various research methods: elemental analysis, mass spectrometry, electrical conductivity, thermogravimetry, IR spectroscopy. It has proved that all complexes are crystal hydrates, belong to heterometallic mixed ligand compounds [Ln(H2O)4(bipy)2]2 [Ge(m-hedp) (m- OH)]6⸱nH2O, Ln=Pr (1); Nd (2); Dy (3); Ho (4); Tm (5); Lu (6); n = 22 (1, 2), 21 (3), 20 (4, 5), 19 (6). Their formation occurs due to the electrostatic interaction of complex cations [Ln(H2O)4(bipy)2]3+ with hexanuclear anions [Ge(m-hedp)(m- OH)]66-. According to the results of measuring the electrical conductivity of dimethylformamide solutions 1–6, it has been established that they belong to triionic electrolytes: λ (in Ohm-1∙сm2∙mol-1) for 1 = 131,3; 2 = 138,8; 3 = 145,8; 4 = 151,1; 5 = 158,3; 6 = 162,7. The cation-anionic type of complexes 1–6 has been confirmed as a result of the analysis of their mass spectrum. The analysis of the mass spectrum showed that the main decomposition direction of the complex is related to the formation of the complex cation fragment [Ln(H2O)4(bipy)2]3+, which corresponds to the most intense peak (m/z = 136, I = 55%). The thermal decomposition of compounds 1–6 includes dehydration, deaquatation, oxidative thermal destruction and the formation of final products as a mixture of Ln2O3 and GeP2O7. On the DTA curves in the interval 70–200 °C the first endothermic effect can be traced, which is accompanied by the removal of a certain number of crystallization and coordination water molecules into the gas phase. Absorption bands of the P-O bond have been detected at ~1053 and ~970 сm-1, that indicates the presence of the fully deprotonated PO32- groups in the composition of complexes. Furthermore, n(OH), ν(Ge–O), d(Ge–OH) bands characteristic for all the previously synthesized compounds with [Ge6(m-OH)6(m-hedp)6]6- anion have been detected in the IR spectra of 1–6. A set of the bands usual for the aromatic molecules n(C–C), das(CH3), ds(CH3), n(Сar=N) has been assigned with 2,2`-bipyridine in the structure of all compounds.
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1-羟乙基二膦酸和2,2′-联吡啶混合配体锗镧系配合物
建立了以1-羟乙基二膦酸和2,2′-联吡啶为原料合成锗和稀土金属(Pr、Nd、Dy、Ho、Tm、Lu)混合金属和混合配体配合物的新方法。这些化合物已经用各种研究方法进行了表征:元素分析、质谱、电导率、热重法、红外光谱。证明了所有配合物均为晶体水合物,属于异质金属混合配体化合物[Ln(H2O)4(bipy)2]2 [Ge(m-hedp) (m- OH)]6⸱nH2O, Ln=Pr (1);和(2);Dy (3);(4);Tm (5);陆(6);n = 22(1,2), 21(3), 20(4,5), 19(6)。它们的形成是由于配合阳离子[Ln(H2O)4(bipy)2]3+与六核阴离子[Ge(m-hedp)(m- OH)]66-的静电相互作用。根据二甲基甲酰胺溶液1 - 6的电导率测定结果,确定其为三离子电解质:λ(欧姆-1∙k - m2∙mol-1)为1 = 133,3;2 = 138,8;3 = 145,8;4 = 151,1;5 = 158,3;6 = 162,7。通过质谱分析,确定了1-6配合物为正阴离子型。质谱分析表明,配合物的主要分解方向与形成配合物阳离子碎片[Ln(H2O)4(bipy)2]3+有关,对应于最强烈的峰(m/z = 136, I = 55%)。化合物1-6的热分解包括脱水、脱水、氧化热破坏和最终产物Ln2O3和GeP2O7的混合物的形成。在70-200°C区间的DTA曲线上可以追踪到第一吸热效应,这伴随着一定数量的结晶和配位水分子进入气相的去除。在~1053和~970 μ m-1处检测到P-O键的吸收带,表明在配合物的组成中存在完全去质子化的PO32-基团。此外,在1-6的红外光谱中还检测到所有含有[Ge6(m-OH)6(m-hedp)6]阴离子的化合物的n(OH)、ν(Ge-O)、d(Ge-OH)带特征。在所有化合物的结构中,芳香分子n(C-C)、das(CH3)、ds(CH3)、n(Сar= n)通常具有的一组带都与2,2′-联吡啶配位。
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