Dipartimento di Scienze Molecolari e Nanosistemi, Università Ca'Foscari Venezia, Via Torino 155, 30170, Venezia Mestre, Italy.
Dalton Trans. 2019 Sep 17;48(36):13580-13588. doi: 10.1039/c9dt01822k.
Novel air stable ruthenium(ii) complexes bearing tridentate ligands bis((1-benzyl-1H-1,2,3-triazol-4-yl)methyl)amine (L1), 1-(1-benzyl-1H-1,2,3-triazol-4-yl)-N-(pyridin-2-ylmethyl)methanamine (L2) or 2-(4-phenyl-1H-1,2,3-triazol-1-yl)-N-(pyridin-2-ylmethyl)ethan-1-amine (L3) were synthesised. The nitrogen based ligands were easily prepared by virtue of click chemistry using cheap and commercially available reagents. The ruthenium complexes were obtained by heating the Ru(PPh3)3Cl2 precursor and the tridentate NNN ligand in toluene under reflux for 2 hours, achieving yields of 82-87%. These complexes were fully characterized by means of NMR, FT-IR and high resolution ESI spectroscopy. The crystal structure of one of the complexes was determined. These complexes showed excellent activity and selectivity in the hydrogenation of ketones and aldehydes. DFT calculations show that complex 3 may react through an outer-sphere catalytic cycle rather than via an inner-sphere mechanism.
新型空气稳定的钌(II)配合物,具有三齿配体双((1-苄基-1H-1,2,3-三唑-4-基)甲基)胺(L1),1-(1-苄基-1H-1,2,3-三唑-4-基)-N-(吡啶-2-基甲基)甲胺(L2)或 2-(4-苯基-1H-1,2,3-三唑-1-基)-N-(吡啶-2-基甲基)乙-1-胺(L3)。这些基于氮的配体很容易通过点击化学合成,使用廉价且市售的试剂。钌配合物通过将 Ru(PPh3)3Cl2 前体和三齿 NNN 配体在甲苯中回流加热 2 小时来获得,产率为 82-87%。这些配合物通过 NMR、FT-IR 和高分辨率 ESI 光谱进行了全面表征。其中一个配合物的晶体结构被确定。这些配合物在酮和醛的氢化中表现出优异的活性和选择性。DFT 计算表明,配合物 3 可能通过外球催化循环而不是内球机制进行反应。