氨基羟基脲与Nd(Ⅲ)及Tb(Ⅲ)的配位化学研究

Coordination Chemistry of Nd(Ⅲ) and Tb(Ⅲ)with 4-hydroxysemicarbazide

  • 摘要: 4-羟基氨基脲(HSC,本文化学式或结构式中以HL表示)可在Purex流程中作为钚的还原剂使用。本文通过吸收光谱滴定法确定HSC与Nd(Ⅲ)在水溶液中可形成金属离子与配体比例为1∶1、1∶2、1∶3的3种配合物Nd(HL)3+、\mathrmNd(\mathrmHL)_2^3+ 和\mathrmNd(\mathrmHL)_3^3+ ,获得了配合物的稳定常数,并通过电位滴定法对中性分子配位模式进行了验证。采用溶剂挥发方法分别制备了配体、质子化配体的高氯酸盐,以及配体与Nd(Ⅲ)、Tb(Ⅲ)的1∶3配合物(金属离子∶配体)的单晶,并采用X射线衍射单晶结构分析方法测定其结构。在Nd(Ⅲ)和Tb(Ⅲ)配合物晶体中,HSC中性分子的羰基氧原子以及肟基氧原子以螯合的形式与中心金属离子形成五元环配位构型。羰基氧原子和肟基氧原子与中心金属离子配位键键长比较的结果表明,晶体中配合物HSC分子配位肟基氧原子上的质子未发生解离。通过水溶液中\mathrmNd(\mathrmHL)_3^3+ 配合物的吸收光谱、Nd(H2O)3(HL)3·3ClO4晶体漫反射光谱及其乙腈溶液吸收光谱的比较,结合Tb(H2O)3(HL)3·3ClO4晶体及其乙腈溶液的荧光光谱及荧光寿命的测定结果,可推测水溶液中HSC与Nd(Ⅲ)、Tb(Ⅲ)形成的配合物中肟基均不解离质子。

     

    Abstract: 4-hydroxysemicarbazide (HSC, HL) could be used as the reducing agent for Pu(Ⅳ) in the Purex process. In this work, three complexes (Nd(HL)3+, \mathrmNd(\mathrmHL)_2^3+ and \mathrmNd(\mathrmHL)_3^3+ ) with the ratio of metal ion to HL at 1∶1, 1∶2 and 1∶3 were proved to exist through the coordination of HSC and Nd(Ⅲ) in aqueous solution by spectrophotometric titration method. Besides, the stability constants of the complexes were determined, as well as the coordination patterns of neutral molecules, which were verified by potentiometric titration. Single crystals, including the ligand, the perchlorate of the protonated ligand, and the 1∶3 complexes \mathrmNd(\mathrmHL)_3^3+ and \mathrmTb(\mathrmHL)_3^3+ were prepared by solvent evaporation method, respectively, with their structures determined by X-ray diffraction. In the above two complexes, the HSC is found to coordinate with the central metal by the carbonyl oxygen atoms and the oxime oxygen atoms, in a five-membered ring. Further, by comparing the length of the Ln-O (carbonyl) bond and the Ln-O (oxime) bond, it is proved that the proton on the oxime oxygen is not dissociated. By comparing the solved molar absorption spectra of the \mathrmNd(\mathrmHL)_3^3+ , the diffuse reflectance spectra of Nd(H2O)3(HL)3·3ClO4 crystals, and its absorption spectra in acetonitrile solution, combining the measurements of the fluorescence spectra and the fluorescence lifetime of Tb(H2O)3(HL)3·3ClO4 in the single crystal and in acetonitrile solution, it could be inferred that in the aqueous solution the proton on the oxime oxygen atom in HSC will not be dissociated, neither. Four novel crystals were synthesized in this study. Amongst, Nd(H2O)3(HL)3·3ClO4 was prepared by slow evaporation method in aqueous solution with the 1∶3 molar ration of Nd(ClO4)3 to HL, which is crystalized in R3c space group with unit cell: a=16.405 6(3) Å, b=16.405 6(3) Å, c=14.829 6(4) Å; α=90°, β=90°, γ=120°; Z=6. Likewise, the Tb(H2O)3(HL)3·3ClO4, which is also crystalized in R3c space group with unit cell: a=16.289 0(7) Å, b=16.289 0(7) Å, c=14.891 9(8) Å; α=90°, β=90°, γ=120°; Z=6. Besides, H2L·ClO4 was cultured in aqueous solution with the 1∶1 molar ration of HL to HClO4, with Pna21 space group and the unit cell: a=8.718 6(8) Å, b=13.809 0(11) Å, c=5.051 9(4) Å; α=90°, β=90°, γ=90°; Z=4. HL was cultured in anhydrous ethanol, with P21/n space group and the unit cell: a=4.099 8(2) Å, b=10.154 0(4) Å, c=8.802 1(4) Å; α=90°, β=99.035(4)°, γ=90°; Z=4.

     

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