Department of Chemistry, University of Michigan, 930 N University Avenue, Ann Arbor, MI, 48109, USA.
Department of Chemistry, Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA, 16802, USA.
Angew Chem Int Ed Engl. 2016 Jun 1;55(23):6685-8. doi: 10.1002/anie.201601742. Epub 2016 Apr 21.
Although the interaction of low-spin ferric complexes with nitric oxide has been well studied, examples of stable high-spin ferric nitrosyls (such as those that could be expected to form at typical non-heme iron sites in biology) are extremely rare. Using the TMG3 tren co-ligand, we have prepared a high-spin ferric NO adduct ({FeNO}(6) complex) via electrochemical or chemical oxidation of the corresponding high-spin ferrous NO {FeNO}(7) complex. The {FeNO}(6) compound is characterized by UV/Visible and IR spectroelectrochemistry, Mössbauer and NMR spectroscopy, X-ray crystallography, and DFT calculations. The data show that its electronic structure is best described as a high-spin iron(IV) center bound to a triplet NO(-) ligand with a very covalent iron-NO bond. This finding demonstrates that this high-spin iron nitrosyl compound undergoes iron-centered redox chemistry, leading to fundamentally different properties than corresponding low-spin compounds, which undergo NO-centered redox transformations.
尽管低自旋三价铁配合物与一氧化氮的相互作用已经得到了很好的研究,但稳定的高自旋三价铁亚硝酰配合物(例如在生物学中典型的非血红素铁位点可能形成的配合物)极为罕见。我们使用 TMG3 三乙撑五胺共配体,通过电化学或化学氧化相应的高自旋亚铁亚硝酰 {FeNO}(7) 配合物,制备了高自旋三价铁一氧化氮加合物 ({FeNO}(6) 配合物)。{FeNO}(6) 化合物通过紫外可见和红外光谱电化学、穆斯堡尔和 NMR 光谱、X 射线晶体学和 DFT 计算进行了表征。数据表明,其电子结构最好描述为一个高自旋铁(IV)中心与三重态 NO(-) 配体结合,具有非常共价的铁-NO 键。这一发现表明,这种高自旋铁亚硝酰化合物经历了铁中心氧化还原化学,导致与相应的低自旋化合物具有根本不同的性质,低自旋化合物经历了以 NO 为中心的氧化还原转化。