Extending the Row of Lanthanide Tetrafluorides: A Combined Matrix-Isolation and Quantum-Chemical Study

被引:14
作者
Vent-Schmidt, Thomas [1 ]
Fang, Zongtang [2 ]
Lee, Zachary [2 ]
Dixon, David [2 ]
Riedel, Sebastian [3 ]
机构
[1] Univ Freiburg, Inst Anorgan & Analyt Chem, D-79104 Freiburg, Germany
[2] Univ Alabama, Dept Chem, Tuscaloosa, AL 35487 USA
[3] Free Univ Berlin, Inst Chem & Biochem, D-14195 Berlin, Germany
基金
美国国家科学基金会;
关键词
electronic structure; fluorine; high oxidation states; lanthanides; matrix-isolation; INFRARED-SPECTRA; MOLECULAR-COMPLEXES; ELECTRIC-DEFLECTION; BASIS-SETS; AB-INITIO; LA-LU; LN; PRASEODYMIUM; GEOMETRIES; ATOMS;
D O I
10.1002/chem.201504182
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Only the neutral tetrafluorides of Ce, Pr, and Tb as well as the [LnF(7)](3-) anions of Dy and Nd, with the metal in the +IV oxidation state, have been previously reported. We report our attempts to extend the row of neutral lanthanide tetrafluorides through the reaction of laser-ablated metal atoms with fluorine and their stabilization and characterization by matrix-isolation IR spectroscopy. In addition to the above three tetrafluorides, we found two new tetrafluorides, (NdF4)-Nd-3 and (DyF4)-Dy-7, both of which are in the +IV oxidation state, which extends this lanthanide oxidation state to two new metals. Our experimental results are supported by quantum-chemical calculations and the role of the lanthanide oxidation state is discussed for both the LnF(4) and [LnF(4)](-) species. Most of the LnF(4) species are predicted to be in the +IV oxidation state and all of the [LnF(4)](-) anions are predicted to be in the +III oxidation state. The LnF(4) species are predicted to be strong oxidizing agents and the LnF(3) species are predicted to be moderate to strong Lewis acids.
引用
收藏
页码:2406 / 2416
页数:11
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