Burgert Ralf, Stokes Sarah T, Bowen Kit H, Schnöckel Hansgeorg
Institute of Inorganic Chemistry, University of Karlsruhe (TH), 76128 Karlsruhe, Germany.
J Am Chem Soc. 2006 Jun 21;128(24):7904-8. doi: 10.1021/ja060613x.
Recently, the icosahedral Al13- cluster has been shown to possess some unusual characteristics due to its special stability (Bergeron, D. E.; et al. Science 2004, 304, 84-87; 2005, 307, 231-235). Here we present reactions of isolated Al13- clusters with hydrogen chloride, following their oxidation through the application of Fourier transform ion cyclotron resonance mass spectrometry. Due to the ultra-low-pressure conditions, the reaction time can be expanded to make one intermediate after another come into view. The following intermediates are generated sequentially, releasing AlCl and H2: Al13HCl-, Al12H-, Al12H2Cl-, Al11H2-, Al12Cl-, and Al11-. The resulting reaction scheme proves to be a molecular model for the dissolution of a metal in an acid, revealing the initial steps of a heretofore unknown fundamental heterogeneous reaction.
最近,二十面体Al13-团簇由于其特殊的稳定性而表现出一些不寻常的特性(伯杰龙,D.E.等人,《科学》2004年,第304卷,第84 - 87页;2005年,第307卷,第231 - 235页)。在此,我们通过傅里叶变换离子回旋共振质谱法对分离出的Al13-团簇进行氧化后,展示了其与氯化氢的反应。由于超低压条件,反应时间得以延长,使得一个又一个中间体得以显现。依次生成以下中间体,释放出AlCl和H2:Al13HCl-、Al12H-、Al12H2Cl-、Al11H2-、Al12Cl-和Al11-。所得反应方案被证明是金属在酸中溶解的分子模型,揭示了迄今为止未知的基本非均相反应的初始步骤。