Tobias A. Teichtmeister, Alexander Hugo Bernhart, Klaus Wurst, Hubert Huppertz
{"title":"High-pressure/high-temperature synthesis of Ln 2CdB5O11(OH) (Ln = Tm, Lu)","authors":"Tobias A. Teichtmeister, Alexander Hugo Bernhart, Klaus Wurst, Hubert Huppertz","doi":"10.1515/znb-2024-0011","DOIUrl":null,"url":null,"abstract":"This report presents work on the orthorhombic phases <jats:italic>Ln</jats:italic> <jats:sub>2</jats:sub>CdB<jats:sub>5</jats:sub>O<jats:sub>11</jats:sub>(OH) (<jats:italic>Ln</jats:italic> = Tm, Lu). The title compounds were synthesized in a Walker-type multianvil device at 7 GPa and 650 °C, and the resulting samples were thoroughly investigated through single-crystal and powder X-ray diffraction methods. Lu<jats:sub>2</jats:sub>CdB<jats:sub>5</jats:sub>O<jats:sub>11</jats:sub>(OH) crystallizes in the space group <jats:italic>Pmna</jats:italic> (no. 53) with the unit cell parameters <jats:italic>a</jats:italic> = 12.772(2), <jats:italic>b</jats:italic> = 4.6017(7), and <jats:italic>c</jats:italic> = 12.481(2) Å. Similar unit cell parameters are observed for the isotypic Tm analogue compound. The crystals have a layered crystal structure built up by four-, five-, and eight-membered rings of corner-sharing [BO<jats:sub>4</jats:sub>] tetrahedra. The structural data are accompanied by attenuated total reflection (ATR) infrared spectra and energy-dispersive X-ray spectroscopy (EDX).","PeriodicalId":23831,"journal":{"name":"Zeitschrift für Naturforschung B","volume":"4 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zeitschrift für Naturforschung B","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/znb-2024-0011","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract
This report presents work on the orthorhombic phases Ln2CdB5O11(OH) (Ln = Tm, Lu). The title compounds were synthesized in a Walker-type multianvil device at 7 GPa and 650 °C, and the resulting samples were thoroughly investigated through single-crystal and powder X-ray diffraction methods. Lu2CdB5O11(OH) crystallizes in the space group Pmna (no. 53) with the unit cell parameters a = 12.772(2), b = 4.6017(7), and c = 12.481(2) Å. Similar unit cell parameters are observed for the isotypic Tm analogue compound. The crystals have a layered crystal structure built up by four-, five-, and eight-membered rings of corner-sharing [BO4] tetrahedra. The structural data are accompanied by attenuated total reflection (ATR) infrared spectra and energy-dispersive X-ray spectroscopy (EDX).
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