Kinetic investigations of the formation of iron(IV) oxido complexes

被引:0
|
作者
Ritz, Florian J. [1 ]
Lerch, Markus [1 ]
Becker, Jonathan [1 ]
Schindler, Siegfried [1 ]
机构
[1] Justus Liebig Univ Giessen, Inst Anorgan & Analyt Chem, Heinrich Buff Ring 17, D-35392 Giessen, Germany
关键词
Iron; chromium; dioxygen activation; oxido complexes; kinetics; MONONUCLEAR NONHEME IRON; SPIN OXOIRON(IV) COMPLEX; SPECTROSCOPIC CHARACTERIZATION; CRYSTAL-STRUCTURE; COPPER;
D O I
10.1080/00958972.2022.2095268
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Oxido iron(IV) complexes are key intermediates in oxygenation reactions in biological systems. They can form during oxidation experiments with various oxidants such as oxygen, hydrogen peroxide, organoiodine compounds, or ozone. However, kinetic studies for these reactions are rare because the intermediates are usually labile. Here the results of a detailed investigation on the oxidation of iron(II) complexes with macrocyclic (e.g. TMC = tetramethylcyclam = 1,4,8,11-tetramethyl-1,4,8,11-tetraaza-cyclotetradecane) ligands are reported that provide a better understanding of the mechanisms of these reactions. For formation of the quite stable oxido iron complex with an amide derivative of TMC, activation parameters with Delta H-double dagger = 28 +/- 4 kJ center dot mol(-1) and Delta S-double dagger = -144 +/- 15 J center dot mol(-1)center dot K-1 could be obtained that allowed postulation of an associative mechanism.
引用
收藏
页码:894 / 907
页数:14
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