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Updated: Mar 28, 2026

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
Published on: June 9, 2023
Sodalite-like rare-earth carbonates: a study of structural transformation and diluted magnetism
Yanyan Wang1, Tian Han1, You-Song Ding1
1Centre for Applied Chemical Research, Frontier Institute of Science and Technology, and MOE Key Laboratory for Nonequilibrium Synthesis and Modulation of Condensed Matter, College of Science, Xi'an Jiaotong University, Xi'an 710054, China. zheng.yanzhen@xjtu.edu.cn.
Abstract:
A series of novel rare earth carbonates, RE3(OH)6(CO3)Cl (RE = Dy, Er, Y), with sodalite-like (SOD-like) zeolite topologies have been successfully synthesized by introducing an appropriate amount of CO3(2-) from NaCO3 or atmospheric carbon dioxide as a template. Single-crystal X-ray diffraction reveals that the structure consists of the RE3(OH)6(3+) cationic framework with a SOD-like topology built from vertex-sharing [RE4(μ3-OH)4] cubes. The CO3(2-) anions seal the 6-ring opening and Cl(-) anions situated in the channels to achieve charge balance. After calcination at 370 °C, the compound RE3(OH)6(CO3)Cl in situ transforms into a new phase formulated as RE3O4Cl. Interestingly, the structure of RE3O4Cl represents a new SOD-like open framework, associated with the removal of the CO3(2-) from RE3(OH)6(CO3)Cl. The samples are characterized by thermogravimetric analysis (TGA), elemental analysis, X-ray photoelectron spectroscopy and magnetic studies. Furthermore, single-molecule magnet behaviours can be observed for the diluted samples of Dy0.0068Y2.9932(OH)6(CO3)Cl and Dy0.0068Y2.9932O4Cl with a Dy/Y molar ratio of up to 1/440 as well as Er0.19Y2.81(OH)6(CO3)Cl with an Er/Y ratio of 1/15, showing dominant single-ion effects.
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