Cuéllar Elena, Diez-Varga Alberto, Torroba Tomás, Domingo-Legarda Pablo, Alemán José, Cabrera Silvia, Martín-Alvarez Jose M, Miguel Daniel, Villafañe Fernando
GIR MIOMeT-IU Cinquima-Química Inorgánica, Facultad de Ciencias, Campus Miguel Delibes, Universidad de Valladolid, 47011 Valladolid, Spain.
Departamento de Química, Facultad de Ciencias, Universidad de Burgos, 09001 Burgos, Spain.
Inorg Chem. 2021 May 17;60(10):7008-7022. doi: 10.1021/acs.inorgchem.0c03389. Epub 2021 Apr 27.
New 1,2-azolylamidino complexes -Ru(bipy)(NH═C(R)az*-κ,) (R = Me, Ph; az* = pz, indz, dmpz) are synthesized via chloride abstraction after a subsequent base-catalyzed coupling of a nitrile with the previously coordinated 1,2-azole. The synthetic procedure allows the easy obtainment of complexes having different electronic and steric 1,2-azoylamidino ligands. All of the compounds have been characterized by H, C, and N NMR and IR spectroscopy and by monocrystal X-ray diffraction. Photophysical studies support their phosphorescence, whereas their electrochemistry reveals reversible Ru/Ru oxidations between +1.13 and +1.25 V (vs SCE). The complexes have been successfully used as catalysts in the photooxidation of different thioethers, the complex -[Ru(bipy)(NH═C(Me)dmpz-κ,)] showing better catalytic performance in comparison to that of [Ru(bipy)]. Moreover, the significant catalytic performance of the dimethylpyrazolylamidino complex is applied to the preparation of the drug modafinil, which is obtained using ambient oxygen as an oxidant. Finally, mechanistic assays suggest that the oxidation reaction follows a photoredox route via oxygen radical anion formation.
新型1,2 - 唑基脒配合物 - Ru(bipy)(NH═C(R)az*-κ,)(R = 甲基、苯基;az* = 吡唑、吲唑、二甲基吡唑)是通过腈与先前配位的1,2 - 唑进行碱催化偶联后,经氯原子抽取合成的。该合成方法能够轻松获得具有不同电子和空间结构的1,2 - 唑基脒配体的配合物。所有化合物均通过氢、碳和氮核磁共振光谱、红外光谱以及单晶X射线衍射进行了表征。光物理研究证实了它们的磷光特性,而电化学研究揭示了在 +1.13至 +1.25 V(相对于饱和甘汞电极)之间存在可逆的Ru/Ru氧化。这些配合物已成功用作不同硫醚光氧化反应的催化剂,与[Ru(bipy)]相比,配合物 - [Ru(bipy)(NH═C(甲基)二甲基吡唑-κ,)]表现出更好的催化性能。此外,二甲基吡唑基脒配合物的显著催化性能被应用于药物莫达非尼的制备,该制备过程使用环境氧气作为氧化剂。最后,机理分析表明氧化反应遵循通过氧自由基阴离子形成的光氧化还原途径。