DIRECTED SYNTHESIS OF MIXED-LIGAND-HETEROMETALLIC XYLARATOGERMANATES OF Co(II) WITH 1,10-PHENANTHROLINE / 2,2'-BIPYRIDINE

E. Chebanenko, I. Seifullina, E. Martsinko
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Abstract

Coordination compounds with complex cations of Co 2+ with 1,10-phenanthroline, 2,2’-bipyridine and tetrameric xylaratogermanate anion were obtained. Their composition and structure were established by the methods of elemental analysis, IR-spectroscopy and thermogravimetric analysis. In the IR-spectrum of I , II bands of asymmetric υas(COO–) (~1686 cm -1 ) and symmetric υs(COO–) (~ 1442 cm -1 ) valence vibrations of carboxylate groups are presented. The presence of υ(C-O) (~ 1069 cm -1 ) band (alcoholic type) and d(C-OH) (~1144 cm -1 ) band, which is typical for the xylaric acid, indicates that not all hydroxyl groupsof the H 5 Xylar ligand are deprotonated. Absorption bands υ(Ge-O) (~737 cm -1 ), υ as (GeOGe) (~851 cm-1) are also detected. They indicate the binding of germanium to xylaric acid and formation of the Ge-O-Ge bridge. The deformation vibration band of the Ge-О-Н (~821 cm -1 ) indicates the implementation of the hydrolyzed form of germanium. There also appear n(ОН)H 2 O, ns(C–Harom.), ν(C-Carom.), n(C-Narom.), δ(С-H) bands, that are typical for crystallization water molecules and 1,10-phenanthroline ( I ), 2,2’-bipyridine ( II ). The thermal destructions of the both compounds are similar. On the thermograms of both compounds one low-temperature effect is presented at 80-270 °С(for I ) and 80-260 °С (for II ) respectively. According to the temperature of elimination and the weight loss (8,75% for I and 14,5% for II ), crystallization water molecules were calculated ( I – 12, II – 20). Due to the mass loss along the thermogravimetric curve at 900 °C, the final products of thermal destruction is a mixture of CoO + GeO 2 . The molecular formulas of complexes I , II are proposed in the accordance of the results of elemental analysis, IR spectroscopy and thermogravimetric analysis: [Сo(phen) 3 ] 2 [(OH) 2 Ge 2 (m-HXylar) 4 Ge 2 (m-OH) 2 ]∙12Н 2 О ( I ), [Сo(bipy) 3 ] 2 [(OH) 2 Ge 2 (m-HXylar) 4 Ge 2 (m-OH) 2 ]∙20Н 2 О ( II ). Their scheme of structure were suggested.
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与1,10-菲罗啉/ 2,2'-联吡啶的Co(II)混合配体-异金属木胶合物的定向合成
得到了Co 2+与1,10-菲罗啉、2,2′-联吡啶和四聚木胶根酸阴离子络合的配位化合物。通过元素分析、红外光谱和热重分析确定了它们的组成和结构。在羧酸基的非对称对称as(COO -) (~1686 cm -1)和对称s(COO -) (~ 1442 cm -1)价态振动的I、II波段的红外光谱中得到。羟基- oh (~1144 cm -1)带和羟基- o (~ 1069 cm -1)带的存在表明,羟基不是所有的羟基都去质子化了。吸光度带υ(Ge-O) (~737 cm-1), υ as (GeOGe) (~851 cm-1)也被检测到。它们表明锗与木酸结合并形成了Ge-O-Ge桥。Ge-О-Н (~821 cm -1)的变形振动带表明锗的水解形式的实现。还出现了n(ОН) h2o, ns(C-Harom .), ν(C-Carom.), n(C-Narom.), δ(С-H)波段,这是典型的结晶水分子和1,10-菲罗啉(I), 2,2′-联吡啶(II)。这两种化合物的热破坏是相似的。在这两种化合物的热图上,分别在80-270°С(对于I)和80-260°С(对于II)表现出低温效应。根据消除温度和失重量(I为8.75%,II为14.5%)计算结晶水分子(I - 12, II - 20)。由于900℃时沿热重曲线的质量损失,热破坏的最终产物是CoO + GeO 2的混合物。根据元素分析、红外光谱和热重分析结果,提出了配合物I、II的分子式:[Сo(phen) 3] 2 [(OH) 2 Ge 2 (m-HXylar) 4 Ge 2 (m-OH) 2]∙12Н 2 О (I), [Сo(bipy) 3] 2 [(OH) 2 Ge 2 (m-HXylar) 4 Ge 2 (m-OH) 2]∙20Н 2 О (II)。提出了他们的结构方案。
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