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Synergy between metals for small molecule activation: Enzymes and bio-inspired complexes

期刊

COORDINATION CHEMISTRY REVIEWS
卷 428, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.ccr.2020.213606

关键词

Homogeneous multimetallic redox catalysts; Metal-metal cooperation; Small molecule activation; Bio-inspired chemistry; Reaction mechanism; Metalloenzymes

资金

  1. French National Agency for Research [ANR-15-IDEX-02]
  2. ARCANE, Programme JCJC [ANR-14-CE06_0002_01]
  3. CBH-EUR-GS [ANR-17-EURE-0003]
  4. ANRDFG [ANR-16-CE92_0012_01]

向作者/读者索取更多资源

Transition metal-driven small molecule activation is essential for the production of fuels and chemicals or energy supply. The use of multimetallic catalysts, where two or more metal centers act in synergy to activate and transform the substrate(s), is widespread both in nature (metalloenzymes) and (bio)inorganic chemistry. Benefits of this strategy in terms of catalytic performances result from cooperation between different metals to bind and activate a single substrate, to activate different substrates reacting together, or with one assisting metal tuning the reactivity of the active metal center.
Transition metal-driven small molecule activation is essential for the production of fuels and chemicals or energy supply. The use of multimetallic catalysts, where two or more metal centers act in synergy to activate and transform the substrate(s), is widespread both in nature (metalloenzymes) and (bio)inorganic chemistry. Benefits of this strategy in terms of catalytic performances result from cooperation between different metals (i) to bind and activate a single substrate, (ii) to activate different substrates reacting together (typically one per metal), or (iii) with one assisting metal tuning the reactivity of the active metal center. In this review, we discuss multimetallic active sites of enzymes and multimetallic synthetic bioinspired complexes, for which the cooperation between metal centers is critical for the activation of small molecules. The following processes are considered: (i) H-2 production(/oxidation) ([FeFe]- and [NiFe]-hydrogenases); (ii) O-2 reduction (cytochrome c oxidase); (iii) CO2 reduction and formation of C-C bonds (NiFe- and MoCu-dependent CO dehydrogenases and acetyl-CoA synthase); (iv) N-2 reduction (Mo-dependent nitrogenase); and (v) N2O reduction (N2O reductase). This overview is expected to contribute to understand the role of metal-metal synergy in enzymes and model complexes and its impact on reactivity. This background, in combination with ligand design, can be exploited for the development of the next generation of bio-inspired multinuclear catalysts with optimized performances. (C) 2020 Elsevier B.V. All rights reserved.

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