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High-pressure synthesis and characterization of the first cerium fluoride borate CeB(2)O(4)F()

CeB(2)O(4)F is the first cerium fluoride borate, which is exclusively built up of one-dimensional, infinite chains of condensed trigonal-planar [BO(3)](3−) groups. This new cerium fluoride borate was synthesized under high-pressure/high-temperature conditions of 0.9 GPa and 1450 °C in a Walker-type...

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Autores principales: Hinteregger, Ernst, Wurst, Klaus, Tribus, Martina, Huppertz, Hubert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738024/
https://www.ncbi.nlm.nih.gov/pubmed/23935215
http://dx.doi.org/10.1016/j.jssc.2013.05.013
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author Hinteregger, Ernst
Wurst, Klaus
Tribus, Martina
Huppertz, Hubert
author_facet Hinteregger, Ernst
Wurst, Klaus
Tribus, Martina
Huppertz, Hubert
author_sort Hinteregger, Ernst
collection PubMed
description CeB(2)O(4)F is the first cerium fluoride borate, which is exclusively built up of one-dimensional, infinite chains of condensed trigonal-planar [BO(3)](3−) groups. This new cerium fluoride borate was synthesized under high-pressure/high-temperature conditions of 0.9 GPa and 1450 °C in a Walker-type multianvil apparatus. The compound crystallizes in the orthorhombic space group Pbca (No. 61) with eight formula units and the lattice parameters a=821.63(5), b=1257.50(9), c=726.71(6) pm, V=750.84(9) Å(3), R(1)=0.0698, and wR(2)=0.0682 (all data). The structure exhibits a 9+1 coordinated cerium ion, one three-fold coordinated fluoride ion and a one-dimensional chain of [BO(3)](3−) groups. Furthermore, IR spectroscopy, Electron Micro Probe Analysis and temperature-dependent X-ray powder diffraction measurements were performed.
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spelling pubmed-37380242013-08-08 High-pressure synthesis and characterization of the first cerium fluoride borate CeB(2)O(4)F() Hinteregger, Ernst Wurst, Klaus Tribus, Martina Huppertz, Hubert J Solid State Chem Article CeB(2)O(4)F is the first cerium fluoride borate, which is exclusively built up of one-dimensional, infinite chains of condensed trigonal-planar [BO(3)](3−) groups. This new cerium fluoride borate was synthesized under high-pressure/high-temperature conditions of 0.9 GPa and 1450 °C in a Walker-type multianvil apparatus. The compound crystallizes in the orthorhombic space group Pbca (No. 61) with eight formula units and the lattice parameters a=821.63(5), b=1257.50(9), c=726.71(6) pm, V=750.84(9) Å(3), R(1)=0.0698, and wR(2)=0.0682 (all data). The structure exhibits a 9+1 coordinated cerium ion, one three-fold coordinated fluoride ion and a one-dimensional chain of [BO(3)](3−) groups. Furthermore, IR spectroscopy, Electron Micro Probe Analysis and temperature-dependent X-ray powder diffraction measurements were performed. Academic Press 2013-08 /pmc/articles/PMC3738024/ /pubmed/23935215 http://dx.doi.org/10.1016/j.jssc.2013.05.013 Text en © 2013 The Authors https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Hinteregger, Ernst
Wurst, Klaus
Tribus, Martina
Huppertz, Hubert
High-pressure synthesis and characterization of the first cerium fluoride borate CeB(2)O(4)F()
title High-pressure synthesis and characterization of the first cerium fluoride borate CeB(2)O(4)F()
title_full High-pressure synthesis and characterization of the first cerium fluoride borate CeB(2)O(4)F()
title_fullStr High-pressure synthesis and characterization of the first cerium fluoride borate CeB(2)O(4)F()
title_full_unstemmed High-pressure synthesis and characterization of the first cerium fluoride borate CeB(2)O(4)F()
title_short High-pressure synthesis and characterization of the first cerium fluoride borate CeB(2)O(4)F()
title_sort high-pressure synthesis and characterization of the first cerium fluoride borate ceb(2)o(4)f()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738024/
https://www.ncbi.nlm.nih.gov/pubmed/23935215
http://dx.doi.org/10.1016/j.jssc.2013.05.013
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