School of Chemistry, The University of Manchester , Manchester, M13 9PL, U.K.
J Am Chem Soc. 2013 Sep 11;135(36):13338-41. doi: 10.1021/ja408589p. Epub 2013 Aug 30.
The 'normal' three-coordinate iron-NHC complex [(IPr)Fe(N'')2] (N″ = N(SiMe3)2) rearranges to its abnormal NHC analogue [(aIPr)Fe(N″)2] (6) on heating, providing a rare abnormal iron-aNHC complex, and the first such three-coordinate complex. The tert-butyl-substituted complex [(I(t)Bu)Fe(N″)2] (4) undergoes a thermal decomposition that has not previously been observed in iron-NHC chemistry, resulting in the bis(imidazole) complex [((t)BuIm)2Fe(N″)2] (7). A mechanism that involves consecutive C-H and C-N activation is proposed to account for the formation of 7.
“正常”的三配位铁-NHC 配合物(IPr)Fe(N'')2在加热时会重排成其异常的 NHC 类似物(aIPr)Fe(N″)2,提供了一种罕见的异常铁-aNHC 配合物,也是首例此类三配位配合物。叔丁基取代的配合物(I(t)Bu)Fe(N″)2经历了一种在铁-NHC 化学中以前从未观察到的热分解,导致双(咪唑)配合物((t)BuIm)2Fe(N″)2的生成。提出了一个涉及连续 C-H 和 C-N 活化的机制来解释 7 的形成。