Bis(aqua)bis(η5-cyclopentadienyl)vanadium(IV) bis(trifluoromethanesulfonate) tetrahydrofuran solvate: Synthesis and characterization

被引：4
|
作者：
Stamatatos, Theocharis C. [1 ,2 ]
Perlepes, Spyros P. [1 ]
Raptopoulou, Catherine P. [3 ]
Terzis, Aris [3 ]
Klouras, Nikolaos [1 ]
机构：
[1] Univ Patras, Dept Chem, Patras 26504, Greece
[2] Brock Univ, Dept Chem, St Catharines, ON L2S 3A1, Canada
[3] NCSR Demokritos, Inst Mat Sci, Aghia Paraskevi 15310, Greece
来源：
INORGANICA CHIMICA ACTA | 2013年 / 394卷
关键词：
Bis(aqua)bis(eta(5)-cyclopentadienyl)vanadium(IV) cation; Crystal structure; Electron paramagnetic resonance spectra; Infrared spectra; Triflate anion; X-RAY-STRUCTURE; COORDINATION CHEMISTRY; CRYSTAL-STRUCTURES; MOLECULAR-STRUCTURE; UNPAIRED ELECTRON; ANTITUMOR AGENTS; COMPLEXES; SPECTRA; DINUCLEAR; ION;
D O I：
10.1016/j.ica.2012.09.038
中图分类号：
O61 [无机化学];
学科分类号：
070301 ; 081704 ;
摘要：
The reactivity pattern of [V(Cp)(2)Cl-2] towards the weakly coordinating CF3SO3 anion in the absence of chelating or bridging organic ligands has been investigated, where Cp is the eta(5)-C5H5 ligand. The synthesis, single-crystal X-ray structure and physical/spectroscopic characterization are reported for the product [V(Cp)(2)(H2O)(2)](CF3SO3)(2)center dot THF (1 center dot THF). The coordination about the V-IV atom, formed by the two H2O molecules and the centroids of the cyclopentadienyl rings, is distorted tetrahedral. The [V(Cp)(2) (H2O)(2)](2+) cation is connected to the triflate anions via hydrogen bonds. Magnetic susceptibility, EPR and IR data are discussed in terms of the nature of bonding and the structure of the complex. (C) 2012 Elsevier B. V. All rights reserved.
引用
收藏
页码：747 / 751
页数：5
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