Evolution of strategies to prepare synthetic mimics of carboxylate-bridged diiron protein active sites

被引:24
|
作者
Do, Loi H. [1 ]
Lippard, Stephen J. [1 ]
机构
[1] MIT, Dept Chem, Cambridge, MA 02139 USA
关键词
Carboxylate-bridged diiron modeling; Dioxygen activation; Biomimetic chemistry; Ligand design; SOLUBLE METHANE MONOOXYGENASE; DIOXYGEN-ACTIVATING CENTERS; LINKED DICARBOXYLATE LIGAND; NONHEME IRON ENZYMES; 1,8-NAPHTHYRIDINE-BASED DINUCLEATING LIGANDS; (FE2O2)-O-IV DIAMOND CORE; DE-NOVO DESIGN; RIBONUCLEOTIDE REDUCTASE; (MU-OXO)BIS(MU-CARBOXYLATO)DIIRON(III) COMPLEXES; FUNCTIONAL MODELS;
D O I
10.1016/j.jinorgbio.2011.08.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We present a comprehensive review of research conducted in our laboratory in pursuit of the long-term goal of reproducing the structures and reactivity of carboxylate-bridged diiron centers used in biology to activate dioxygen for the conversion of hydrocarbons to alcohols and related products. This article describes the evolution of strategies devised to achieve these goals and illustrates the challenges in getting there. Particular emphasis is placed on controlling the geometry and coordination environment of the diiron core, preventing formation of polynuclear iron clusters, maintaining the structural integrity of model complexes during reactions with dioxygen, and tuning the ligand framework to stabilize desired oxygenated diiron species. Studies of the various model systems have improved our understanding of the electronic and physical characteristics of carboxylate-bridged diiron units and their reactivity toward molecular oxygen and organic moieties. The principles and lessons that have emerged from these investigations will guide future efforts to develop more sophisticated diiron protein model complexes. (C) 2011 Elsevier Inc. All rights reserved.
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页码:1774 / 1785
页数:12
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