Two halide-containing cesium manganese vanadates: Synthesis, characterization, and magnetic properties

Tiffany M. Smith Pellizzeri, Michael A. McGuire, Colin D. McMillen, Yimei Wen, George Chumanov, Joseph W. Kolis

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

Two new halide-containing cesium manganese vanadates have been synthesized by a high-temperature (580 °C) hydrothermal synthetic method from aqueous brine solutions. One compound, Cs3Mn(VO3)4Cl, (1) was prepared using a mixed cesium hydroxide/chloride mineralizer, and crystallizes in the polar noncentrosymmetric space group Cmm2, with a = 16.7820(8) Å, b = 8.4765(4) Å, c = 5.7867(3) Å. This structure is built from sinusoidal zig-zag (VO3)n chains that run along the b-axis and are coordinated to Mn2+ containing (MnO4Cl) square-pyramidal units that are linked together to form layers. The cesium cations reside between the layers, but also coordinate to the chloride ion, forming a cesium chloride chain that also propagates along the b-axis. The other compound, Cs2Mn(VO3)3F, (2) crystallizes in space group Pbca with a = 7.4286(2) Å, b = 15.0175(5) Å, c = 19.6957(7) Å, and was prepared using a cesium fluoride mineralizer. The structure is comprised of corner sharing octahedral Mn2+ chains, with trans fluoride ligands acting as bridging units, whose ends are capped by (VO3)n vanadate chains to form slabs. The cesium atoms reside between the manganese vanadate layers, and also play an integral part in the structure, forming a cesium fluoride chain that runs along the b-axis. Both compounds were characterized by single-crystal X-ray diffraction, powder X-ray diffraction, and single-crystal Raman spectroscopy. Additionally, the magnetic properties of 2 were investigated. Above 50 K, it displays behavior typical of a low dimensional system with antiferromagnetic interactions, as to be expected for linear chains of manganese(ii) within the crystal structure.

Original languageEnglish
Pages (from-to)2619-2627
Number of pages9
JournalDalton Transactions
Volume47
Issue number8
DOIs
StatePublished - 2018

Funding

We are indebted to the National Science Foundation NSF-DMR-1410727 for financial support of this work. Magnetic studies were supported by the US Department of Energy, Office of Science, Basic Energy Sciences, Materials Sciences and Engineering Division (M. A. M.).

FundersFunder number
National Science FoundationNSF-DMR-1410727
U.S. Department of Energy
Office of Science
Basic Energy Sciences
Division of Materials Sciences and Engineering
National Science Foundation

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