Issue 14, 2016

The first examples of 1-D organic hybrid lanthanoid thioarsenates based on two [AsVS4]3− linkage modes

Abstract

A series of new 1-D organic hybrid lanthanoid thioarsenates [Ln(dap)2]2(μ–η1111-AsS4)(μ–η11-AsVS4)]n {Ln = Ce (Ia), Pr (Ib), Nd (Ic), and Sm (Id); dap = diaminopropane} have been prepared under solvothermal conditions and structurally characterized. Compounds Ia–d contain two [AsVS4]3− linkage modes, namely μ–η1111-AsVS4 and μ–η11-AsVS4, which are linked alternately with [Ln(dap)2]3+ groups into 1-D neutral chains [Ln(dap)2]2(μ–η1111-AsVS4)(μ–η11-AsVS4)]n, which represent the first examples of 1-D organic hybrid lanthanoid thioarsenates based on two [AsVS4]3− linkage modes. To learn more about the influence of lanthanide contraction on the formation of lanthanoid thioarsenates, five organic hybrid lanthanoid thioarsenates [Ln(dap)3AsVS4] [Ln = Tb (IIa), Dy (IIb), Ho (IIIc), and Er (IIId)] and [Er(dien)2AsVS4] (III, dien = diethylenetriamine) are also provided. Both II and III contain neutral lanthanide-centred complexes, where the tetrahedral anion [AsVS4]3− acts as a chelating ligand to the complex [Ln(dap)3]3+/[Er(dien)2]3+ cation. Their optical properties have been characterized by UV-vis spectra, and the density functional theory calculation of Ia has been performed.

Graphical abstract: The first examples of 1-D organic hybrid lanthanoid thioarsenates based on two [AsVS4]3− linkage modes

Supplementary files

Article information

Article type
Paper
Submitted
09 六月 2015
Accepted
10 八月 2015
First published
10 八月 2015

Dalton Trans., 2016,45, 6015-6022

The first examples of 1-D organic hybrid lanthanoid thioarsenates based on two [AsVS4]3− linkage modes

R. Zhao, X. Liu, J. Zhou, H. Xiao, H. Zou, L. Fu, Q. Tang and X. Tan, Dalton Trans., 2016, 45, 6015 DOI: 10.1039/C5DT02188J

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