Qiu Youai, Tian Cong, Massignan Leonardo, Rogge Torben, Ackermann Lutz
Institut für Organische und Biomolekulare Chemie, Georg-August-Universität Göttingen, Tammannstraße 2, 37077, Göttingen, Germany.
Angew Chem Int Ed Engl. 2018 May 14;57(20):5818-5822. doi: 10.1002/anie.201802748. Epub 2018 Apr 23.
Electrocatalysis has been identified as a powerful strategy for organometallic catalysis, and yet electrocatalytic C-H activation is restricted to strongly N-coordinating directing groups. The first example of electrocatalytic C-H activation by weak O-coordination is presented, in which a versatile ruthenium(II) carboxylate catalyst enables electrooxidative C-H/O-H functionalization for alkyne annulations in the absence of metal oxidants; thereby exploiting sustainable electricity as the sole oxidant. Mechanistic insights provide strong support for a facile organometallic C-H ruthenation and an effective electrochemical reoxidation of the key ruthenium(0) intermediate.
电催化已被认为是有机金属催化的一种强大策略,然而电催化C-H活化仅限于强N配位导向基团。本文展示了通过弱O配位实现电催化C-H活化的首个实例,其中一种通用的羧酸钌(II)催化剂能够在无金属氧化剂的情况下实现用于炔烃环化的电氧化C-H/O-H官能团化;从而利用可持续电力作为唯一的氧化剂。机理研究为关键的钌(0)中间体的 facile 有机金属C-H钌化和有效的电化学再氧化提供了有力支持。