Bukowski Michael R, Koehntop Kevin D, Stubna Audria, Bominaar Emile L, Halfen Jason A, Münck Eckard, Nam Wonwoo, Que Lawrence
Department of Chemistry and Center for Metals in Biocatalysis, University of Minnesota, Minneapolis, MN 55455, USA.
Science. 2005 Nov 11;310(5750):1000-2. doi: 10.1126/science.1119092. Epub 2005 Oct 27.
Thiolate-ligated oxoiron(IV) centers are postulated to be the key oxidants in the catalytic cycles of oxygen-activating cytochrome P450 and related enzymes. Despite considerable synthetic efforts, chemists have not succeeded in preparing an appropriate model complex. Here we report the synthesis and spectroscopic characterization of [FeIV(O)(TMCS)]+ where TMCS is a pentadentate ligand that provides a square pyramidal N4(SR)apical, where SR is thiolate, ligand environment about the iron center, which is similar to that of cytochrome P450. The rigidity of the ligand framework stabilizes the thiolate in an oxidizing environment. Reactivity studies suggest that thiolate coordination favors hydrogen-atom abstraction chemistry over oxygen-atom transfer pathways in the presence of reducing substrates.
硫醇盐配位的氧代铁(IV)中心被认为是氧活化细胞色素P450及相关酶催化循环中的关键氧化剂。尽管进行了大量的合成研究,但化学家们尚未成功制备出合适的模型配合物。在此,我们报告了[FeIV(O)(TMCS)]+的合成及光谱表征,其中TMCS是一种五齿配体,它提供了一个四方锥型的N4(SR) 配位环境(其中SR为硫醇盐)围绕铁中心,这与细胞色素P450的配位环境相似。配体骨架的刚性在氧化环境中稳定了硫醇盐。反应性研究表明,在存在还原底物的情况下,硫醇盐配位有利于通过氢原子夺取反应而非氧原子转移途径进行化学反应。