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Models for Nonheme Iron Intermediates: Structural Basis for Tuning the Spin States of Fe(TPA) Complexes

机译:非血红素铁中间体的模型:调整Fe(TPA)配合物自旋态的结构基础

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摘要

Our efforts to model the oxygen activation chemistry of nonheme iron enzymes have yielded transient intermediates with novel properties. These properties can be dramatically affected by the introduction of a 6-methyl substituent on the pendant pyridines of the tetradentate ligand TPA(TPA=tris(2-pyridylmethyl)amine). A series of Fe(TPA) complexes has thus been synthesized and characterized to provide the structural basis fro these dramatic effects.
机译:我们为非血红素铁酶的氧激活化学建模的努力已产生具有新颖性质的瞬时中间体。通过在四齿配体TPA(TPA =三(2-吡啶基甲基)胺)的侧基吡啶上引入6-甲基取代基可以显着影响这些性质。因此已经合成了一系列Fe(TPA)配合物,并对其进行了表征,从而为这些显着作用提供了结构基础。

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