Scheurrell Kerstin, B Martins Inês C, Murray Claire, Emmerling Franziska
Federal Institute for Materials Research and Testing (BAM), Berlin, Germany.
Department of Chemistry, Humboldt-Universität zu Berlin, Berlin, Germany.
Phys Chem Chem Phys. 2023 Sep 13;25(35):23637-23644. doi: 10.1039/d3cp02883f.
Mechanochemistry has proven to be a highly effective method for the synthesis of organic compounds. We studied the kinetics of the catalyst-free Knoevenagel reaction between 4-nitrobenzaldehyde and malononitrile, activated and driven by ball milling. The reaction was investigated in the absence of solvents (neat grinding) and in the presence of solvents with different polarities (liquid-assisted grinding). The reaction was monitored using time-resolved Raman spectroscopy and powder X-ray diffraction (PXRD). Our results indicate a direct relationship between solvent polarity and reaction kinetics, with higher solvent polarity leading to faster product (2-(4-nitrobenzylidone)malononitrile) formation. For the first time, we were able to isolate and determine the structure of an intermediate 2-(hydroxy(4-nitrophenyl)methyl)malononitrile based on PXRD data.
机械化学已被证明是一种合成有机化合物的高效方法。我们研究了在球磨激活和驱动下,4-硝基苯甲醛与丙二腈之间无催化剂的Knoevenagel反应动力学。该反应在无溶剂(纯研磨)和存在不同极性溶剂(液相助磨)的条件下进行研究。使用时间分辨拉曼光谱和粉末X射线衍射(PXRD)对反应进行监测。我们的结果表明溶剂极性与反应动力学之间存在直接关系,溶剂极性越高,产物(2-(4-硝基亚苄基)丙二腈)形成越快。我们首次能够基于PXRD数据分离并确定中间体2-(羟基(4-硝基苯基)甲基)丙二腈的结构。