Liedtke Theresa, Spannring Peter, Riccardi Ludovico, Gansäuer Andreas
Kekulé-Institut für Organische Chemie und Biochemie, Universität Bonn, Gerhard Domagk-Straße 1, 53121, Bonn, Germany.
Angew Chem Int Ed Engl. 2018 Apr 23;57(18):5006-5010. doi: 10.1002/anie.201800731. Epub 2018 Mar 26.
A cyclic-voltammetry-based screening method for Cp TiX-catalyzed reactions is introduced. Our mechanism-based approach enables the study of the influence of various additives on the electrochemically generated active catalyst Cp TiX, which is in equilibrium with catalytically inactive [Cp TiX ] . Thioureas and ureas are most efficient in the generation of Cp TiX in THF. Knowing the precise position of the equilibrium between Cp TiX and [Cp TiX ] allowed us to identify reaction conditions for the bulk electrolysis of Cp TiX complexes and for Cp TiX-catayzed radical arylations without having to carry out the reactions. Our time- and resource-efficient approach is of general interest for the design of catalytic reactions that proceed in single-electron steps.
介绍了一种基于循环伏安法的Cp TiX催化反应筛选方法。我们基于机理的方法能够研究各种添加剂对电化学生成的活性催化剂Cp TiX的影响,Cp TiX与催化惰性的[Cp TiX ]处于平衡状态。硫脲和脲在四氢呋喃中生成Cp TiX最为有效。了解Cp TiX与[Cp TiX ]之间平衡的精确位置,使我们能够确定Cp TiX配合物本体电解以及Cp TiX催化的自由基芳基化反应的条件,而无需进行实际反应。我们这种节省时间和资源的方法对于设计以单电子步骤进行的催化反应具有普遍意义。