INVESTIGATION OF NEW POLYMER COMPLEXES BASED ON Yb(III) β-DIKETONATES

N. Ivakha, O. Berezhnytska, O. Rohovtsov, O. Trunova, S. Smola
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Abstract

The metal polymers based on mono- and heteroligand β-diketonate complexes of Yb(III) with 2,7-dimethyl-octen-1-dione-3,5, 2,6-dimethyl-heptene-1-dione-3, 5 and with phenanthroline was synthesized. It has been defined that the coordination environment of the central ion remains unchanged during radical polymerization. The shape and position of the bands in the electronic absorption spectra are similar to the corresponding monomeric β-diketonate metal complexes, and slight shifts indicate deformation of the elementary unit of the metal polymer during the formation of the polymer chain. It is shown that the polymerization process lead to an increasing in the thermal stability of polymer complexes in comparison with monomeric analogues. An increase in the emission of metal polymers in comparison with monomeric complexes was established by the method of luminescent spectroscopy, which is due to energy, steric, and structural-mechanical factors.
基于Yb(III) β-双酮酸酯的新型聚合物配合物的研究
合成了Yb(III)与2,7-二甲基辛酮-1-二酮- 3,5,2,6 -二甲基庚烯-1-二酮-3,5和邻菲罗啉的单寡和异寡β-二酮酸配合物的金属聚合物。在自由基聚合过程中,中心离子的配位环境保持不变。电子吸收光谱中带的形状和位置与相应的单体β-二酮酸金属配合物相似,轻微的位移表明金属聚合物在聚合物链形成过程中发生了基本单元的变形。结果表明,与单体类似物相比,聚合过程提高了聚合物配合物的热稳定性。通过发光光谱法确定了金属聚合物比单体配合物的发光增加,这是由于能量、位阻和结构力学因素所致。
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