Ren Hailong, Zhou Yu-Peng, Bai Yunping, Cui Chunming, Driess Matthias
State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin, 300071, P. R. China.
Department of Chemistry: Metalorganics and Inorganic Materials Sekr C2, Technische Universität Berlin, Strasse des 17. Juni 135, Berlin, 10623, Germany.
Chemistry. 2017 Apr 27;23(24):5663-5667. doi: 10.1002/chem.201605937. Epub 2017 Apr 5.
C-H Borylation of arenes has been a subject of great interest recently because of its atom-economy and the wide applicability of borylated products in value-added synthesis. A new bis(silylene)cobalt(II) complex bearing a bis(N-heterocyclic silylene)-pyridine pincer ligand (SiNSi) has been synthesized and structurally characterized. It enabled the regioselective catalytic C-H borylation of pyridines, furans, and fluorinated arenes. Notably, it exhibited complementary regioselectivity for the borylation of fluorinated arenes compared to previously known catalytic systems, demonstrating that N-heterocyclic silylene donors have enormous potential in metal-catalyzed catalytic applications.
芳烃的碳-氢键硼化反应近来备受关注,因其具有原子经济性以及硼化产物在增值合成中的广泛适用性。一种新型的带有双(N-杂环硅烯)-吡啶钳形配体(SiNSi)的双(硅烯)钴(II)配合物已被合成并进行了结构表征。它能够实现吡啶、呋喃和氟化芳烃的区域选择性催化碳-氢键硼化反应。值得注意的是,与先前已知的催化体系相比,它在氟化芳烃的硼化反应中表现出互补的区域选择性,这表明N-杂环硅烯供体在金属催化应用中具有巨大潜力。