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
相关论文
共 50 条
  • [41] Conformational isomerism in methyl cyanoacetate: A combined matrix-isolation infrared spectroscopy and molecular orbital study
    Reva, ID
    Ilieva, SV
    Fausto, R
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2001, 3 (19) : 4235 - 4241
  • [42] Vibrational spectrum and molecular structure of triphenylamine monomer: A combined matrix-isolation FTIR and theoretical study
    Reva, I
    Lapinski, L
    Chattopadhyay, N
    Fausto, R
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2003, 5 (18) : 3844 - 3850
  • [43] Combined matrix-isolation infrared and theoretical DFT and ab initio study of the nonionized valine conformers
    Stepanian, SG
    Reva, ID
    Radchenko, ED
    Adamowicz, L
    JOURNAL OF PHYSICAL CHEMISTRY A, 1999, 103 (22): : 4404 - 4412
  • [44] Ferrocene - ozone reactions: A matrix-isolation and DFT study
    Kugel, Roger
    Pinelo, Laura
    Ault, Bruce
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2015, 249
  • [45] SPIN CONVERSION IN AMMONIA - A NITROGEN MATRIX-ISOLATION STUDY
    FREDIN, L
    NELANDER, B
    CHEMICAL PHYSICS, 1981, 60 (02) : 181 - 186
  • [46] A combined matrix-isolation infrared spectroscopy and MO study of 1-amino-2-propanol
    Cacela, C
    Fausto, R
    Duarte, ML
    VIBRATIONAL SPECTROSCOPY, 2001, 26 (01) : 113 - 131
  • [47] Matrix-isolation and computational study of the HKrCCH•••HCCH complex
    Willmann, Knut
    Vent-Schmidt, Thomas
    Rasanen, Markku
    Riedel, Sebastian
    Khriachtchev, Leonid
    RSC ADVANCES, 2015, 5 (45) : 35783 - 35791
  • [48] STRUCTURE OF BENZENE HALOGEN COMPLEXES - MATRIX-ISOLATION STUDY
    FREDIN, L
    NELANDER, B
    MOLECULAR PHYSICS, 1974, 27 (04) : 885 - 898
  • [49] Photoisomerization of the perfluoroallyl radical: a FTIR matrix-isolation study
    Baskir, EG
    Korolev, VA
    Nefedov, OM
    MENDELEEV COMMUNICATIONS, 2000, (04) : 125 - 126
  • [50] INDIUM DICARBONYL - MATRIX-ISOLATION ESR AND IR STUDY
    HATTON, WG
    HACKER, HP
    KASAI, PH
    JOURNAL OF PHYSICAL CHEMISTRY, 1989, 93 (04): : 1328 - 1332