Al-Afyouni Malik H, Fillman Kathlyn L, Brennessel William W, Neidig Michael L
Department of Chemistry, University of Rochester , Rochester, New York 14627, United States.
J Am Chem Soc. 2014 Nov 5;136(44):15457-60. doi: 10.1021/ja5080757. Epub 2014 Oct 28.
While iron-catalyzed Kumada cross-coupling reactions with simple iron salts have been known since the early 1970s, the nature of the in situ-formed iron species remains elusive. Herein, we report the synthesis of the homoleptic tetralkyliron(III) ferrate complex [MgCl(THF)5][FeMe4] from the reaction of FeCl3 with MeMgBr in THF. Upon warming, this distorted square-planar S = (3)/2 species converts to the S = (1)/2 species originally observed by Kochi and co-workers with concomitant formation of ethane, consistent with its intermediacy in the reduction pathway of FeCl3 to generate the reduced iron species involved in catalysis.
自20世纪70年代初以来,人们就知道简单铁盐催化的铁催化 Kumada 交叉偶联反应,但原位生成的铁物种的性质仍然难以捉摸。在此,我们报道了由 FeCl3 与 MeMgBr 在四氢呋喃(THF)中反应合成均配型四烷基高铁(III)酸盐配合物[MgCl(THF)5][FeMe4]。升温时,这种扭曲的平面正方形 S = (3)/2 物种转变为最初由 Kochi 及其同事观察到的 S = (1)/2 物种,并伴随乙烷的形成,这与其在 FeCl3 还原途径中生成参与催化的还原铁物种的中间体作用相一致。