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Self-assembly of three-dimensional oxalate-bridged alkali(I)-lanthanide(III) heterometal-organic frameworks

Abstract

Three isostructural three-dimensional (3D) oxalate bridged alkali(I)-lanthanide(III) heterometal-organic frameworks with the general formula [Ln8Na4(ox)10(μ3-OH)8]·MeOH·10H2O (Ln = Tb (1), Dy (2), Er (3)) have been assembled from the solvothermal reactions of oxalic acid (H2ox) with Ln(NO3)3 and Na2CO3. These compounds crystallize in the tetragonal I4/m space group and exhibit a 3D six-connected uninodal net of pcu alpha-Po primitive cubic type based on tetranuclear [Ln4(μ3-OH)4] cubane clusters. Among them, compound 1 exhibits a multifunctional luminescent probe property for the detection of acetone, toluene, and Fe3+ ion based on the fluorescence quenching mechanisms. The magnetic investigations of 1-3 indicate antiferromagnetic coupling between the spin centers Ln3+ ions. In addition, 1 and 3 show negligible adsorption capacity of carbon dioxide.

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Supplementary files

Article information


Submitted
22 Jan 2020
Accepted
02 Jun 2020
First published
23 Jun 2020

CrystEngComm, 2020, Accepted Manuscript
Article type
Paper

Self-assembly of three-dimensional oxalate-bridged alkali(I)-lanthanide(III) heterometal-organic frameworks

N. Ponjan, F. Kielar, W. Dungkaew, K. Kongpatpanich, H. Zenno, S. Hayami, M. Sukwattanasinitt and K. Chainok, CrystEngComm, 2020, Accepted Manuscript , DOI: 10.1039/D0CE00099J

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