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酶和合成试剂中高价铁氧物种的反应活性:多种状态的故事。

Reactivity of high-valent iron-oxo species in enzymes and synthetic reagents: a tale of many states.

作者信息

Shaik Sason, Hirao Hajime, Kumar Devesh

机构信息

Department of Organic Chemistry and The Lise Meitner-Minerva Center for Computational Quantum Chemistry, The Hebrew University of Jerusalem, Givat Ram Campus, 91904 Jerusalem, Israel.

出版信息

Acc Chem Res. 2007 Jul;40(7):532-42. doi: 10.1021/ar600042c. Epub 2007 May 9.

Abstract

The Account discusses the phenomenon of two-state reactivity (TSR) or multistate reactivity (MSR) in high-valent metal-oxo reagents, projecting its wide-ranging applicability starting from the bare species, through the reagents made by Que, Nam, and collaborators, to the Mn(V)-oxo substituted polyoxometalate, all the way to Compound I species of heme enzymes. The Account shows how the behaviors of all these variegated species derive from a simple set of electronic structure principles. Experimental trends that demonstrate TSR and MSR are discussed. Diagnostic mechanistic probes are proposed for the TSR/MSR scenario, based on kinetic isotope effect, stereochemical studies, and magnetic- and electric-field effects.

摘要

本综述讨论了高价金属氧试剂中的双态反应性(TSR)或多态反应性(MSR)现象,预测了其广泛的适用性,从单纯的物种开始,到Que、Nam及其合作者制备的试剂,再到锰(V)氧取代的多金属氧酸盐,一直到血红素酶的化合物I物种。该综述展示了所有这些多样物种的行为如何源自一组简单的电子结构原理。文中讨论了证明TSR和MSR的实验趋势。基于动力学同位素效应、立体化学研究以及磁场和电场效应,针对TSR/MSR情况提出了诊断性机理探针。

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