A thiolate-ligated nonheme oxoiron(IV) complex relevant to cytochrome P450

被引:229
作者
Bukowski, MR
Koehntop, KD
Stubna, A
Bominaar, EL
Halfen, JA [1 ]
Münck, E
Nam, W
Que, L
机构
[1] Univ Wisconsin, Dept Chem, Eau Claire, WI 54702 USA
[2] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Ctr Met Biocatalysis, Minneapolis, MN 55455 USA
[4] Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
[5] Ewha Womans Univ, Dept Chem, Div Nano Sci, Seoul 120750, South Korea
[6] Ewha Womans Univ, Ctr Biomimet Syst, Seoul 120750, South Korea
关键词
D O I
10.1126/science.1119092
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 [Fe-IV(O)(TMCS)](+) where TMCS is a pentadentate ligand that provides a square pyramidal N-4(SR)(apical), where SR is thiotate, 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.
引用
收藏
页码:1000 / 1002
页数:3
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