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Variable Structures and One-Dimensional-Canting Antiferromagetism Found in Fluoride Selenates, A2Mn(SeO4)F3(A = K, Rb, Cs)

Authors
Zhu, T.Lee, S.Zhang, X.Yang, H.Jin, Y.Jin, Y.Choi, K.-Y.Lü, M.
Issue Date
6-Sep-2021
Publisher
American Chemical Society
Citation
Inorganic Chemistry, v.60, no.17, pp 13707 - 13717
Pages
11
Journal Title
Inorganic Chemistry
Volume
60
Number
17
Start Page
13707
End Page
13717
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/49132
DOI
10.1021/acs.inorgchem.1c02084
ISSN
0020-1669
1520-510X
Abstract
Three new alkali-metal manganese fluoride selenates, A2Mn(SeO4)F3 (A = K, Rb, Cs), were prepared through hydrothermal redox reactions. The products consisted of one-dimensional polymeric anionic ∞[Mn(SeO4)F3]2- chains, where the A+ cations are connected by O and/or F atoms to form blocks with two-dimensional layers. A2Mn(SeO4)F3 (A= Rb, Cs) is isostructural with the monoclinic space group P21/c, while K2Mn(SeO4)F3 crystallizes in the orthorhombic space group Pbcn. A2Mn(SeO4)F3 (A = K, Rb, Cs) forms spin chains of Mn3+ with different Mn-F-Mn bridges, which showed canting antiferromagnetic behaviors. Single-crystal magnetic measurements revealed that the magnetic moments of the Mn ions were more canted for larger alkali-metal compounds in an antiferromagnetically ordered state. © 2021 American Chemical Society.
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