Mo Jiayu, Müller Thomas, Oliveira João C A, Demeshko Serhiy, Meyer Franc, Ackermann Lutz
Institut für Organische und Biomolekulare Chemie, Georg-August-Universität Göttingen, Tammannstraße 2, 37077, Göttingen, Germany.
Institut für Anorganische Chemie, Georg-August-Universität Göttingen, Tammannstraße 4, 37077, Göttingen, Germany.
Angew Chem Int Ed Engl. 2019 Sep 9;58(37):12874-12878. doi: 10.1002/anie.201904110. Epub 2019 Jul 30.
An iron-catalyzed C-H/N-H alkyne annulation was realized by using a customizable clickable triazole amide under exceedingly mild reaction conditions. A unifying mechanistic approach combining experiment, spectroscopy, kinetics, and computation provided strong support for facile C-H activation by a ligand-to-ligand hydrogen transfer (LLHT) mechanism. Combined Mössbauer spectroscopic analysis and DFT calculations were indicative of high-spin iron(II) species as the key intermediates in the C-H activation manifold.
通过使用可定制的可点击三唑酰胺,在极其温和的反应条件下实现了铁催化的C-H/N-H炔烃环化反应。结合实验、光谱学、动力学和计算的统一机理方法为通过配体到配体氢转移(LLHT)机制实现的简便C-H活化提供了有力支持。穆斯堡尔光谱分析和DFT计算相结合表明,高自旋铁(II)物种是C-H活化过程中的关键中间体。