Fachbereich Chemie, Philipps-Universität, Hans-Meerwein-Str. 4, 35043, Marburg, Germany.
Institut für Anorganische Chemie, Universität Göttingen, Tammannstr. 4, 37077, Göttingen, Germany.
Chemistry. 2021 Apr 7;27(20):6348-6353. doi: 10.1002/chem.202100336. Epub 2021 Mar 5.
A [Fe-S-Fe] subunit with a single sulfide bridging two low-coordinate iron ions is the supposed active site of the iron-molybdenum co-factor (FeMoco) of nitrogenase. Here we report a dinuclear monosulfido bridged diiron(II) complex with a similar complex geometry that can be oxidized stepwise to diiron(II/III) and diiron(III/III) complexes while retaining the [Fe-S-Fe] core. The series of complexes has been characterized crystallographically, and electronic structures have been studied using, inter alia, Fe Mössbauer spectroscopy and SQUID magnetometry. Further, cleavage of the [Fe-S-Fe] unit by CS is presented.
一个 [Fe-S-Fe] 亚基,其中一个硫桥连两个低配位铁离子,被认为是氮酶的铁-钼辅因子 (FeMoco) 的活性位点。在这里,我们报告了一个具有类似的双核单硫桥联二铁(II)配合物,该配合物可以分步氧化为二铁(II/III)和二铁(III/III)配合物,同时保留[Fe-S-Fe] 核。该系列配合物已通过晶体学进行了表征,并使用 Fe Mössbauer 光谱和 SQUID 磁强计等方法研究了其电子结构。此外,还提出了 CS 对 [Fe-S-Fe] 单元的裂解。