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EPR and Mössbauer Spectroscopy and DFT Analysis of a High-Spin FeIV-oxo Complex

机译:一个高自旋FeIV氧复合物的EpR和穆斯堡尔谱和DFT分析

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摘要

The kinetically competent oxidant in non-heme iron enzymes is a high-spin FeIV-oxo species, which are not as well characterized as the intermediate-spin species of heme systems. The present work gives a detailed characterization of the structurally similar [FeIVH3buea(O)]-, [FeIIIH3buea(O)]2- and [FeIIIH3buea(OH)]- (H3buea = tris[(N'-tert-butylureaylato)-N-ethylene]aminato) complexes using Mössbauer and dual-frequency/dual-mode electron paramagnetic resonance (EPR) spectroscopies. The [FeIVH3buea(O)]- complex has a high-spin (S = 2) configuration imposed from the C3-symmetric ligand. EPR spectroscopy of the [FeIVH3buea(O)]- complex is the first documented example of an EPR signal from an FeIV-oxo complex, demonstrating the ability to detect and quantify FeIV species with EPR spectroscopy. Quantitative simulations allowed determination of the zero-field parameter, D = +4.7 cm-1, and the species concentration. Density functional theory calculations of the zero-field parameter are found to be in agreement with the experimental value and indicate the major contribution to the D-value is from spin–orbit coupling of the ground state with an excited S = 1 electronic configuration at 1.2 eV. 17O isotope enrichment experiments allowed a determination of the hyperfine constant 170Az = 10 MHz for [FeIVH3buea(O)]- and 170Ay = 8 MHz, 170Az = 12 MHz for [FeIIIH3buea(OH)]-. The isotropic hyperfine constant (170Aiso = -16.8 MHz) was derived from the experimental value to allow a quantitative determination of the spin polarization (ρp = 0.56) of the oxo p-orbitals of the Fe-oxo bond in [FeIVH3buea(O)]-. This is the first experimental determination for non-heme complexes, and indicates significant covalency in the Fe-oxo bond. High-field Mössbauer spectroscopy gave an 57Fe >Adip tensor of (+5.6, +5.3, -10.9) MHz and Aiso = -25.9 MHz for the [FeIVH3buea(O)]- complex, and DFT calculations are in agreement with the nuclear parameters of the complex.
机译:非血红素酶的动力学氧化剂是高旋转Fe IV -oxo物种,其并不表征为血红系统的中间旋转物种。本作本作的详细表征在结构相似的[Fe IV H3Buea(O)] - ,[Fe III H3buea(O)] 2 - 和[Fe III h3buea(OH)] - (h3buea = tris [(n'-叔丁基脲基盐酸盐)-n-乙烯]氨基纳胺)配合物使用Mössbauer和双频/双模电子顺磁共振(EPR)光谱。 [Fe IV H3Buea(O)] - 复合物具有从C3对称配体施加的高旋转(S = 2)构型。 [Fe IV H3Buea(O)] - 复合物的EPR光谱是来自Fe IV -oxo的EPR信号的第一个记录实例复杂,展示了用EPR光谱检测和定量Fe IV 物种的能力。定量仿真允许确定零场参数D = + 4.7cm -1 ,以及物种浓度。发现零场参数的密度功能理论计算与实验值一致,并指示对D值的主要贡献是从1.2处具有激励的S = 1电子构造的地面状态的旋转轨道耦合EV。 17 o同位素富集实验允许测定Hyclefine常数 170 az = 10mHz,用于[Fe Iv h3buea(o)] - 170 ay = 8 mHz, 170 az = 12mHz,用于[fe III h3buea(OH)] - 。从实验值衍生出各向同性高血常数( 170 Aiso = -16.8MHz),以允许定量测定Fe-oxo的氧代P-轨道的旋转极化(ρp= 0.56)粘合在[Fe IV H3Buea(O)] - 。这是非血红素复合物的第一次实验测定,并表明Fe-Oxo键的显着共价。高场Mössbauer光谱法给出了(+5.6,+ 5.3,-10.9)MHz和 ISO = - [Fe IV H 3 buea(o)] - 复合物,DFT计算与核参数一致复杂的。

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