Computational thermodynamic study on the complexes of Am(III) with tridentate N-donor ligands

	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)
刊名	NEW JOURNAL OF CHEMISTRY
	2015
卷号	39 期号:10 页码:7716-7729
通讯作者	王东琪
英文摘要	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).
学科主题	Chemistry
类目[WOS]	Chemistry, Multidisciplinary
收录类别	SCI
WOS记录号	WOS:000362355200027
公开日期	2016-05-03
内容类型	期刊论文
源URL	[http://ir.ihep.ac.cn/handle/311005/228767]
专题	高能物理研究所_院士
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.