硼酸镧镉的新多晶型系列 LnCdB6O10(OH)3 (Ln = Sm-Er)的高压/高温合成

Tobias A. Teichtmeister, Alexander Hugo Bernhart, Klaus Wurst, Gunter Heymann, Hubert Huppertz
{"title":"硼酸镧镉的新多晶型系列 LnCdB6O10(OH)3 (Ln = Sm-Er)的高压/高温合成","authors":"Tobias A. Teichtmeister, Alexander Hugo Bernhart, Klaus Wurst, Gunter Heymann, Hubert Huppertz","doi":"10.1515/zkri-2024-0063","DOIUrl":null,"url":null,"abstract":"We report on the synthesis, structure determination, and characterization of a new series of compounds <jats:italic>Ln</jats:italic>CdB<jats:sub>6</jats:sub>O<jats:sub>10</jats:sub>(OH)<jats:sub>3</jats:sub> (<jats:italic>Ln</jats:italic> = Sm–Er). Syntheses were carried out in a Walker-type multianvil device at 7 GPa and 650 °C. Structure determinations revealed the coexistence of an orthorhombic and a monoclinic polymorph, depending on the ionic radius of the lanthanoid cation. The orthorhombic structural variants crystallize non-centrosymmetrically in the space group <jats:italic>Pna</jats:italic>2<jats:sub>1</jats:sub> (no. 33), while the monoclinic modifications crystallize in space group <jats:italic>P</jats:italic>2<jats:sub>1</jats:sub>/<jats:italic>c</jats:italic> (no. 14). Both modifications display a layered crystal structure built up by a repeating [B<jats:sub>6</jats:sub>O<jats:sub>13</jats:sub>]<jats:sup>8−</jats:sup> building block as their main structural feature.","PeriodicalId":23855,"journal":{"name":"Zeitschrift für Kristallographie - Crystalline Materials","volume":"26 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"High-pressure/high-temperature synthesis of a new polymorphic series of lanthanoid cadmium borates, LnCdB6O10(OH)3 (Ln = Sm–Er)\",\"authors\":\"Tobias A. Teichtmeister, Alexander Hugo Bernhart, Klaus Wurst, Gunter Heymann, Hubert Huppertz\",\"doi\":\"10.1515/zkri-2024-0063\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"We report on the synthesis, structure determination, and characterization of a new series of compounds <jats:italic>Ln</jats:italic>CdB<jats:sub>6</jats:sub>O<jats:sub>10</jats:sub>(OH)<jats:sub>3</jats:sub> (<jats:italic>Ln</jats:italic> = Sm–Er). Syntheses were carried out in a Walker-type multianvil device at 7 GPa and 650 °C. Structure determinations revealed the coexistence of an orthorhombic and a monoclinic polymorph, depending on the ionic radius of the lanthanoid cation. The orthorhombic structural variants crystallize non-centrosymmetrically in the space group <jats:italic>Pna</jats:italic>2<jats:sub>1</jats:sub> (no. 33), while the monoclinic modifications crystallize in space group <jats:italic>P</jats:italic>2<jats:sub>1</jats:sub>/<jats:italic>c</jats:italic> (no. 14). Both modifications display a layered crystal structure built up by a repeating [B<jats:sub>6</jats:sub>O<jats:sub>13</jats:sub>]<jats:sup>8−</jats:sup> building block as their main structural feature.\",\"PeriodicalId\":23855,\"journal\":{\"name\":\"Zeitschrift für Kristallographie - Crystalline Materials\",\"volume\":\"26 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-03-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zeitschrift für Kristallographie - Crystalline Materials\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1515/zkri-2024-0063\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zeitschrift für Kristallographie - Crystalline Materials","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/zkri-2024-0063","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

我们报告了一系列新化合物 LnCdB6O10(OH)3(Ln = Sm-Er)的合成、结构测定和表征。合成是在 7 GPa 和 650 ℃ 的沃克型多坩埚装置中进行的。结构测定结果表明,根据镧系阳离子的离子半径,正方体和单斜多晶体并存。正方晶结构变体在空间群 Pna21(编号 33)中以非中心对称方式结晶,而单斜晶变体则在空间群 P21/c(编号 14)中结晶。这两种变体的主要结构特征都是由重复的 [B6O13]8- 结构单元构建的层状晶体结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-pressure/high-temperature synthesis of a new polymorphic series of lanthanoid cadmium borates, LnCdB6O10(OH)3 (Ln = Sm–Er)
We report on the synthesis, structure determination, and characterization of a new series of compounds LnCdB6O10(OH)3 (Ln = Sm–Er). Syntheses were carried out in a Walker-type multianvil device at 7 GPa and 650 °C. Structure determinations revealed the coexistence of an orthorhombic and a monoclinic polymorph, depending on the ionic radius of the lanthanoid cation. The orthorhombic structural variants crystallize non-centrosymmetrically in the space group Pna21 (no. 33), while the monoclinic modifications crystallize in space group P21/c (no. 14). Both modifications display a layered crystal structure built up by a repeating [B6O13]8− building block as their main structural feature.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信