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Computational thermodynamic study on the complexes of Am(III) with tridentate N-donor ligands
Liang, YN; Yang X(杨霞); Yang, X; Ding, SD; Li, SJ; Wang, F; Chai, ZF; Wang, DQ; Chai ZF(柴之芳); Wang DQ(王东琪)
2015
发表期刊NEW JOURNAL OF CHEMISTRY
卷号39期号:10页码:7716-7729
通讯作者王东琪
文章类型Article
摘要To assess the role of the lateral triazine group of 2,6-bis(1,2,4-triazin-3-yl) pyridine (BTP) when coordinated to Am(III), three tridentate N-donor ligands, i.e. BTP, 6-(-2-pyridyl)-2-pyridyl (hemi-BTP), and 2,2':6'2 ''-terpyridine (TPY), have been used to construct coordination complexes with Am(III), and the structures and binding modes of these complexes have been investigated using the B3LYP functional. The 1 : 1 and 1 : 2 (metal : ligand) type complexes, based on our calculations, form mainly via reactions Am(H2O)(3)(NO3)(3) + L -> AmL(NO3)(3) + 3H(2)O and [Am(H2O)(6)(NO3)(2)](+) + 2L -> [AmL2(NO3)(2)](+) + 6H(2)O. The Gibbs free energy changes were in the order of TPY > hemi-BTP > BTP, independent of the presence of nitrate ions in the complexes. We show that in 1 : 1 type complexes substitution of electron-donating groups to the three ligands can enhance their binding ability. From analysis of NPA charge and Mayer Bond Order, it is found that the value of binding free energy is correlated with charge transfers between the central metal and the ligand: the larger the ligand-to-metal charge transfer, the more negative the binding energy, and meanwhile, the smaller the Mayer bond order of the Am-N bonds. This suggests that the interaction between Am(III) and the tridentate ligands has a strong ionic feature, which is confirmed by the quantum theory of atoms-in-molecules (QTAIM) topological analysis. According to our calculations, the presence of the triazine group in BTP and hemi-BTP does not improve the binding affinity of the ligand to Am(III), compared to TPY, but facilitates the ligand to adopt a conformation that favors to coordinate with Am3+ than others via a dynamic isomerization process, and the electron-donating groups on the triazine group may enhance the charge transfer between Am(III) and the ligand, and thus stabilize the complex. We tentatively propose that the facile conversion between the conformations of BTP, which is more difficult for TPY and hemi-BTP, may significantly contribute to its higher affinity towards binding with Am(III).
学科领域Chemistry
DOI10.1039/c5nj01285f
收录类别SCI
WOS类目Chemistry, Multidisciplinary
WOS记录号WOS:000362355200027
引用统计
文献类型期刊论文
条目标识符http://ir.ihep.ac.cn/handle/311005/228767
专题院士
多学科研究中心
推荐引用方式
GB/T 7714
Liang, YN,Yang X,Yang, X,et al. Computational thermodynamic study on the complexes of Am(III) with tridentate N-donor ligands[J]. NEW JOURNAL OF CHEMISTRY,2015,39(10):7716-7729.
APA Liang, YN.,杨霞.,Yang, X.,Ding, SD.,Li, SJ.,...&王东琪.(2015).Computational thermodynamic study on the complexes of Am(III) with tridentate N-donor ligands.NEW JOURNAL OF CHEMISTRY,39(10),7716-7729.
MLA Liang, YN,et al."Computational thermodynamic study on the complexes of Am(III) with tridentate N-donor ligands".NEW JOURNAL OF CHEMISTRY 39.10(2015):7716-7729.
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