Gas-phase synthesis and characterization of heteroleptic divalent germanium compounds by FVT/UV-PES

被引:12
作者
Chrostowska, Anna [1 ]
Lemierre, Virginie [1 ]
Dargelos, Alain [1 ]
Baylere, Patrick [1 ]
Leigh, William J. [2 ]
Rima, Ghassoub [3 ]
Weber, Lothar [4 ]
Schimmel, Michaela [4 ]
机构
[1] Univ Pau & Pays Adour, Inst Pluridisciplinaire Rech Environm & Mat, UMR 5254, F-64053 Pau 9, France
[2] McMaster Univ, Dept Chem, Hamilton, ON L8S 4M1, Canada
[3] Univ Toulouse 3, UMR 5069, F-31062 Toulouse 4, France
[4] Univ Bielefeld, Fak Chem, D-33615 Bielefeld, Germany
基金
加拿大自然科学与工程研究理事会;
关键词
Germylene; Low-coordinated germanium compounds; UV photoelectron spectroscopy; Ionization energies; Quantum mechanical calculation; Flash vacuum thermolysis; DENSITY-FUNCTIONAL THEORY; PHOTOELECTRON-SPECTRA; STABLE SILYLENES; IONIZATION-POTENTIALS; ELECTRONIC-STRUCTURE; EXCITATION-ENERGIES; BIVALENT GERMANIUM; GERMYLENES; SPECTROSCOPY; SI(NRCH2CH2NR);
D O I
10.1016/j.jorganchem.2008.09.069
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The. ash vacuum thermolysis/UV photoelectron spectroscopic (FVT/UV-PES) technique has been applied for the synthesis of three cyclic germanediyls containing oxo-thio, oxo-amino, and thio-amino substitution at germanium. The three compounds (4b, 5b and 6b) were prepared from the corresponding 3,4dimethyl-1-germacyclopent-3-enes (4a, 5a and 6a) by thermal cheletropic elimination, and the photoelectron spectra of both sets of molecules were measured. The course of the thermolysis reactions has also been confirmed by mass spectrometric methods and the results of chemical trapping experiments. The assignment of the PE spectral bands for the two series of molecules has been carried out with the aid of time dependent DFT (TD-DFT) and outer valence green's function (OVGF) calculations. The results indicate that the strong sigma-withdrawing effect of oxygen and the strong pi-donating effect of nitrogen are the two main factors affecting the electronic structures of these germylene derivatives. (C) 2008 Elsevier B. V. All rights reserved.
引用
收藏
页码:43 / 51
页数:9
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