Synthesis of divalent europium borate via in situ reductive techniques

Matthew J. Polinski; Justin N. Cross; Eric M. Villa; Jian Lin; Evgeny V. Alekseev; Wulf Depmeier; Thomas E. Albrecht-Schmitt

doi:10.1021/ic400781x

Synthesis of divalent europium borate via in situ reductive techniques

Matthew J. Polinski, Justin N. Cross, Eric M. Villa, Jian Lin, Evgeny V. Alekseev, Wulf Depmeier, Thomas E. Albrecht-Schmitt

Research output: Contribution to journal › Article › peer-review

14 Scopus citations

Abstract

A new divalent europium borate, Eu[B₈O₁₁(OH) ₄], was synthesized by two different in situ reductive methodologies starting with a trivalent europium starting material in a molten boric acid flux. The two in situ reductive techniques employed were the use of HI as a source of H₂ gas and the use of a Zn amalgam as a reductive, reactive surface. While both of these are known reductive techniques, the title compound was synthesized in both air and water which demonstrates that strict anaerobic conditions need not be employed in conjunction with these reductive methodologies. Herein, we report on the structure, spectroscopy, and synthetic methodologies relevant to Eu[B₈O₁₁(OH)₄]. We also report on a europium doping study of the isostructural compound Sr[B ₈O₁₁(OH)₄] where the amount of doped Eu ²⁺ ranges from 2.5 to 11%.

Original language	English (US)
Pages (from-to)	8099-8105
Number of pages	7
Journal	Inorganic Chemistry
Volume	52
Issue number	14
DOIs	https://doi.org/10.1021/ic400781x
State	Published - Jul 15 2013
Externally published	Yes

All Science Journal Classification (ASJC) codes

Physical and Theoretical Chemistry
Inorganic Chemistry

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title = "Synthesis of divalent europium borate via in situ reductive techniques",

abstract = "A new divalent europium borate, Eu[B8O11(OH) 4], was synthesized by two different in situ reductive methodologies starting with a trivalent europium starting material in a molten boric acid flux. The two in situ reductive techniques employed were the use of HI as a source of H2 gas and the use of a Zn amalgam as a reductive, reactive surface. While both of these are known reductive techniques, the title compound was synthesized in both air and water which demonstrates that strict anaerobic conditions need not be employed in conjunction with these reductive methodologies. Herein, we report on the structure, spectroscopy, and synthetic methodologies relevant to Eu[B8O11(OH)4]. We also report on a europium doping study of the isostructural compound Sr[B 8O11(OH)4] where the amount of doped Eu 2+ ranges from 2.5 to 11%.",

author = "Polinski, {Matthew J.} and Cross, {Justin N.} and Villa, {Eric M.} and Jian Lin and Alekseev, {Evgeny V.} and Wulf Depmeier and Albrecht-Schmitt, {Thomas E.}",

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T1 - Synthesis of divalent europium borate via in situ reductive techniques

AU - Polinski, Matthew J.

AU - Cross, Justin N.

AU - Villa, Eric M.

AU - Lin, Jian

AU - Alekseev, Evgeny V.

AU - Depmeier, Wulf

AU - Albrecht-Schmitt, Thomas E.

PY - 2013/7/15

Y1 - 2013/7/15

N2 - A new divalent europium borate, Eu[B8O11(OH) 4], was synthesized by two different in situ reductive methodologies starting with a trivalent europium starting material in a molten boric acid flux. The two in situ reductive techniques employed were the use of HI as a source of H2 gas and the use of a Zn amalgam as a reductive, reactive surface. While both of these are known reductive techniques, the title compound was synthesized in both air and water which demonstrates that strict anaerobic conditions need not be employed in conjunction with these reductive methodologies. Herein, we report on the structure, spectroscopy, and synthetic methodologies relevant to Eu[B8O11(OH)4]. We also report on a europium doping study of the isostructural compound Sr[B 8O11(OH)4] where the amount of doped Eu 2+ ranges from 2.5 to 11%.

AB - A new divalent europium borate, Eu[B8O11(OH) 4], was synthesized by two different in situ reductive methodologies starting with a trivalent europium starting material in a molten boric acid flux. The two in situ reductive techniques employed were the use of HI as a source of H2 gas and the use of a Zn amalgam as a reductive, reactive surface. While both of these are known reductive techniques, the title compound was synthesized in both air and water which demonstrates that strict anaerobic conditions need not be employed in conjunction with these reductive methodologies. Herein, we report on the structure, spectroscopy, and synthetic methodologies relevant to Eu[B8O11(OH)4]. We also report on a europium doping study of the isostructural compound Sr[B 8O11(OH)4] where the amount of doped Eu 2+ ranges from 2.5 to 11%.

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