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Structure and Properties of the Non‐Centrosymmetric Manganese(II) Borate Mn5(BO3)3OH

The rose‐colored compound Mn5(BO3)3OH was synthesized under high‐pressure/high‐temperature conditions of 2.5 GPa and 973 K in a Walker‐type multianvil press. Single‐crystal X‐ray structure determination yielded the non‐centrosymmetric monoclinic space group Pm (no. 6) with the lattice parameters a =...

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Bibliographic Details
Published in:European journal of inorganic chemistry 2019-09, Vol.2019 (34), p.3854-3862
Main Authors: Falkowski, Viktoria, Zeugner, Alexander, Bayarjargal, Lkhamsuren, Saxer, Andreas, Ruck, Michael, Huppertz, Hubert
Format: Article
Language:English
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Summary:The rose‐colored compound Mn5(BO3)3OH was synthesized under high‐pressure/high‐temperature conditions of 2.5 GPa and 973 K in a Walker‐type multianvil press. Single‐crystal X‐ray structure determination yielded the non‐centrosymmetric monoclinic space group Pm (no. 6) with the lattice parameters a = 329.71(1), b = 1384.92(5), c = 902.37(3) pm, and β = 107.92(1)°. The presence of the hydroxide group is ascertained by vibrational spectroscopy. Magnetization experiments in the range from 300 to 14 K revealed paramagnetic behavior with antiferromagnetic ordering below 14 K and an effective magnetic moment of 12.2 µB per formula unit. The acentric nature of the material was verified by second harmonic generation measurements, yielding a considerably strong intensity (Isample/Iquartz = 11.14). Additionally, thermal investigations showed a several‐step transformation to Mn2OBO3 upon heating under air. High‐pressure synthesis of acentric Mn5(BO3)3OH: By means of high‐pressure/high temperature synthesis, the non‐centrosymmetric manganese(II) compound Mn5(BO3)3OH was obtained and characterized by single‐crystal and powder X‐ray diffraction. Additionally, vibrational spectroscopy, UV/Vis, thermoanalytical, magnetic, and SHG measurements were performed.
ISSN:1434-1948
1099-0682
DOI:10.1002/ejic.201900769