Gimeno Magali, Aguilera Maria Camila, Fleischauer Valerie E, Brennessel William W, Neidig Michael L
Inorganic Chemistry Laboratory, University of Oxford, South Parks Road, Oxford, OX1 3QR, UK.
Department of Chemistry, University of Rochester, 120 Trustee Rd, Rochester, NY14627, USA.
Angew Chem Int Ed Engl. 2025 Jan 2;64(1):e202413566. doi: 10.1002/anie.202413566. Epub 2024 Nov 2.
While iron-catalyzed C(sp)-C(sp) cross-couplings have been widely studied and developed in the last decade, alkyl-alkyl cross-coupling systems with iron remain underdeveloped despite the importance of C(sp)-C(sp) bonds in organic synthesis. A major challenge to the development of these reactions is the current lack of fundamental insight into ligand effects and organoiron intermediates that enable effective alkyl-alkyl couplings. The current study addresses this longstanding limitation using a combination of Fe Mössbauer spectroscopy, SC-XRD (single-crystal X-ray diffraction) and reactivity studies of alkyl-alkyl coupling with iron-Xantphos to define the in situ formed iron-Xantphos intermediates in catalysis. Combined with detailed reactivity studies, the nature of the key mechanistic pathways in catalysis and ligands effects to achieve effective alkyl-alkyl cross-coupling over competing β-H elimination pathways are probed. Overall, these foundational studies provide a platform for future bespoke ligand and pre-catalyst design for alkyl-alkyl cross-coupling methods development with sustainable iron catalysis.
尽管在过去十年中铁催化的C(sp)-C(sp)交叉偶联反应已得到广泛研究和发展,但铁催化的烷基-烷基交叉偶联体系仍未得到充分发展,尽管C(sp)-C(sp)键在有机合成中具有重要意义。这些反应发展的一个主要挑战是目前对配体效应和有机铁中间体缺乏基本认识,而这些是实现有效烷基-烷基偶联所必需的。本研究通过结合Fe穆斯堡尔光谱、SC-XRD(单晶X射线衍射)以及铁-联二萘酚膦配体的烷基-烷基偶联反应性研究,来确定催化过程中原位形成的铁-联二萘酚膦中间体,从而解决这一长期存在的局限性。结合详细的反应性研究,探讨了催化过程中关键机理途径的本质以及配体效应,以实现有效烷基-烷基交叉偶联,同时避免竞争性的β-H消除途径。总体而言,这些基础研究为未来定制配体和预催化剂设计提供了一个平台,以推动可持续铁催化的烷基-烷基交叉偶联方法的发展。