首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Comparative insight into electronic properties and reactivities toward C-H bond activation by iron(IV)-nitrido, iron(IV)-oxo, and iron(IV)-sulfido complexes: A theoretical investigation
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Comparative insight into electronic properties and reactivities toward C-H bond activation by iron(IV)-nitrido, iron(IV)-oxo, and iron(IV)-sulfido complexes: A theoretical investigation

机译:铁(IV)-硝态铁,铁(IV)-氧代和铁(IV)-硫键络合物对电子性质和C-H键活化反应性的比较见解:理论研究

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A range of novel octahedral iron(IV)-nitrido complexes with the TMC ligand (TMC = 1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane) in the equatorial plane and one axial ligand trans to the nitrido have been designed theoretically, and a systematic comparative study of their geometries, electronic properties, and reactivities in hydrogen atom abstraction reactions regarding the iron(IV)-oxo and -sulfido counterparts has been performed using density-functional theory methods. Further, the relative importance of the axial ligands on the reactivity of the iron(IV)-nitrido systems is probed by sampling the reactions of CH_4 with [Fe~(IV)-N(TMC)(L _(ax))]~(n+), (L_(ax) = none, CH_3CN, CF _3CO_2 ~-, N_3 ~-, Cl ~-, NC~-, and SR~-). As we find, one hydrogen atom is abstracted from the methane by the iron(IV)-nitrido species, leading to an Fe~(III)(N)-H moiety together with a carbon radical, similar to the cases by the iron(IV)-oxo and -sulfido compounds. DFT calculations show that, unlike the well-known iron(IV)-oxo species with the S = 1 ground state where two-state reactivity (TSR) was postulated to involve, the iron(IV)-nitrido and -sulfido complexes stabilize in a high-spin (S = 2) quintet ground state, and they appear to proceed on the single-state reactivity via a dominantly and energetically favorable low-lying quintet spin surface in the H-abstraction reaction that enjoys the exchange-enhanced reactivity. It is further demonstrated that the iron(IV)-nitrido complexes are capable of hydroxylating C-H bond of methane, and potential reactivities as good as the iron(IV)-oxo and -sulfido species have been observed. Additionally, analysis of the axial ligand effect reveals that the reactivity of iron(IV)-nitrido oxidants in the quintet state toward C-H bond activation enhances as the electron-donating ability of the axial ligand weakens.
机译:在赤道平面上具有TMC配体(TMC = 1,4,8,11-四甲基-1,4,8,11-四氮杂环十四烷)和一个轴向配体的一系列新型八面体铁(IV)-氮杂配合物从理论上设计了亚硝基,并且已经使用密度泛函理论方法对它们的几何形状,电子性质以及与铁(IV)-氧代和-硫代对应物有关的氢原子抽象反应中的反应性进行了系统的比较研究。此外,通过对CH_4与[Fe〜(IV)-N(TMC)(L _(ax))]〜的反应进行采样,可以探究轴向配体对铁(IV)-硝铁体系反应性的相对重要性。 (n +),(L_(ax)= none,CH_3CN,CF _3CO_2〜-,N_3〜-,Cl〜-,NC〜-和SR〜-)。我们发现,铁(IV)-氮原子从甲烷中抽出一个氢原子,导致一个Fe〜(III)(N)-H部分以及一个碳原子团,这与铁的情况类似( IV)-氧代和-硫代化合物。 DFT计算表明,与众所周知的S = 1基态的铁(IV)-氧代物种不同(其中假定具有二态反应性(TSR)),铁(IV)-氮基和-磺基络合物在高自旋(S = 2)五重态基态,并且它们似乎通过占优势的,能量上有利的低洼五重态自旋表面在享有交换增强反应性的H吸收反应中以单态反应性进行。进一步证明,铁(IV)-氮杂配合物能够羟基化甲烷的C-H键,并且已经观察到与铁(IV)-氧代和-硫代物质一样好的潜在反应性。另外,对轴向配体效应的分析表明,随着轴向配体的给电子能力减弱,五重态的铁(IV)-硝态氧化剂对C-H键活化的反应性增强。

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