School of Chemistry and Chemical Engineering, Xi'an Shiyou University, Xi'an 710065, China.
Department of Chemistry, Nankai University, TianJin 300071, China.
Molecules. 2018 Sep 10;23(9):2304. doi: 10.3390/molecules23092304.
We aimed to develop new effective catalysts for the synthesis of propylene carbonate from propylene oxide and carbon dioxide. A kind of MCl coordination complex was fabricated based on the chelating tridentate ligand 2,6-bis[1-(phenylimino)ethyl] pyridine (). The obtained products were characterized by elemental analysis, infrared spectroscopy, ultraviolet spectroscopy, thermogravimetric analysis, and single-crystal X-ray diffraction. It was found that the catalytic activity of the complexes with different metal ions, the same ligand differed and co-catalyst, where the order of greatest to least catalytic activity was > > . The catalytic system composed of complex and DMAP proved to have the better catalytic performance. The yields for complex systems was 86.7% under the reaction conditions of 100 °C, 2.5 MPa, and 4 h. The TOF was 1026 h¹ under the reaction conditions of 200 °C, 2.5 MPa, and 1 h. We also explored the influence of time, pressure, temperature, and reaction substrate concentration on the catalytic reactions. A hypothetical catalytic reaction mechanism is proposed based on density functional theory (DFT) calculations and the catalytic reaction results.
我们旨在开发用于由环氧丙烷和二氧化碳合成碳酸丙烯酯的新型有效催化剂。基于螯合三齿配体 2,6-双[1-(苯基亚氨基)乙基]吡啶()合成了一种 MCl 配位配合物。通过元素分析、红外光谱、紫外光谱、热重分析和单晶 X 射线衍射对所得产物进行了表征。结果发现,具有不同金属离子的配合物的催化活性、相同配体的不同和助催化剂的催化活性不同,其中催化活性的顺序为> > >。由配合物和 DMAP 组成的催化体系表现出更好的催化性能。在 100°C、2.5 MPa 和 4 h 的反应条件下,配合物 体系的产率为 86.7%。在 200°C、2.5 MPa 和 1 h 的反应条件下,TOF 为 1026 h¹。我们还研究了时间、压力、温度和反应底物浓度对催化反应的影响。基于密度泛函理论(DFT)计算和催化反应结果提出了一个假设的催化反应机理。