联吡啶羧酸酯和邻菲罗啉羧酸酯与三价锕系元素和镧系元素的配合物:结合强度和结构

Jun Liu, Liang Yang, Baihua Chen, Xingliang Li, Yanqiu Yang
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引用次数: 1

摘要

采用溶剂萃取、电位法和晶体学研究了配体(2,2′-联吡啶-6-羧酸酯(BiPCA)和1,10-菲罗啉-2-羧酸酯(PhenCA)与三价锕系元素(An)如Am(III)和Cm(III),镧系元素(Ln)如Nd(III)、Sm(III)和Eu(III)的结合强度。这两种配体对锕系元素的选择性都优于镧系元素,对基团内的Ln(III)或An(III)具有半径选择性。相比之下,PhenCA在这些功能上比BiPCA更突出。Nd(III)/Eu(III)与BiPCA和PhenCA的单晶结构表明BiPCA和PhenCA是三齿化合物,并通过两个芳香n给体和一个羧基o给体与Nd(III)/Eu(III)螯合。PhenCA与中心原子的配位键比BiPCA短,这与PhenCA在溶液中对相同镧系阳离子的结合强度比BiPCA强的事实相一致。然而,对于具有相同配体的镧系配合物,Nd(III)和Eu(III)之间的配位键没有规律的趋势。
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Complexes of bipyridinecarboxylate and phenanthrolinecarboxylate with trivalent actinides and lanthanides: Binding strength and structure

The binding strengths of ligand 2,2ʹ-bipyridine-6-carboxylate (BiPCA) and 1,10-phenanthroline-2-carboxylate (PhenCA) with trivalent actinides (An) like Am(III) and Cm(III), and lanthanides (Ln) like Nd(III), Sm(III), and Eu(III) were investigated by solvent extraction, potentiometry, and crystallography. Both ligands exhibit good actinides selectivity over lanthanides and radius selectivity for intragroup Ln(III) or An(III). In comparison, PhenCA is more prominent than BiPCA in these capabilities. Single crystal structures of the Nd(III)/Eu(III) with BiPCA and PhenCA illustrate that BiPCA, as well as PhenCA, is tridentate and chelates with Nd(III)/Eu(III) by two aromatic N-donors and a carboxyl O-donor. PhenCA exhibits shorter coordination bonds to the central atom than BiPCA, in agreement with the fact that in solution PhenCA behaves stronger binding strength than BiPCA to the same lanthanide cation. However, for the lanthanide complexes with the same ligand, no regular trend of the coordination bonds has been observed between Nd(III) and Eu(III).

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