Iron-catalyzed dehydrogenation reactions and their applications in sustainable energy and catalysis

被引:82
作者
Balaraman, Ekambaram [1 ,2 ]
Nandakumar, Avanashiappan [1 ]
Jaiswal, Garima [1 ,2 ]
Sahoo, Manoj K. [1 ,2 ]
机构
[1] CSIR, Catalysis Div, Natl Chem Lab, Dr Homi Bhabha Rd, Pune 411008, Maharashtra, India
[2] Acad Sci & Innovat Res AcSIR, New Delhi 110025, India
基金
日本学术振兴会;
关键词
FORMIC-ACID DEHYDROGENATION; CHEMICAL HYDROGEN STORAGE; METAL-DIENE COMPLEXES; MEDIATED 2+2+1 CYCLOADDITIONS; LIGAND-EXCHANGE REACTION; AMMONIA-BORANE; ORGANIC-SYNTHESIS; HOMOGENEOUS CATALYSTS; BENZYLIC ALCOHOLS; PINCER COMPLEX;
D O I
10.1039/c7cy00879a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Inspired by nature, chemists have designed new catalysts in the pursuit of selective bond activation and chemical transformations. Emergent biological systems often use earth-abundant first-row transition elements as catalytically active sites to facilitate specific and highly selective chemical processes. The design of a new catalytic system based on abundant and inexpensive catalysts, particularly the iron-based catalysts, for fundamentally significant synthetic transformations under environmentally benign conditions is an important paradigm in chemical synthesis. In recent times, iron-based catalytic systems have shown unprecedented reactivity in the acceptorless dehydrogenation reactions of feedstock chemicals, with the liberation of molecular hydrogen as the by-product, and have enabled greener chemical synthetic methods and alternative energy storage systems. Indeed, it has been demonstrated that the proper design of iron catalysts by judiciously choosing ligands, can aid in the development of new sustainable energy storage systems and catalysis. This tutorial review focuses on the recent development of iron-based dehydrogenation reactions of fundamentally important feedstock, as a route to sustainable chemical synthesis and energy storage applications. The emerging area of the iron-based dehydrogenation strategy provides an opportunity to make industrially applicable, cost-effective and environmentally benign catalytic systems.
引用
收藏
页码:3177 / 3195
页数:19
相关论文
共 85 条
[41]  
Knölker HJ, 1999, ANGEW CHEM INT EDIT, V38, P2064, DOI 10.1002/(SICI)1521-3773(19990712)38:13/14<2064::AID-ANIE2064>3.0.CO
[42]  
2-W
[43]  
Knölker HJ, 1999, ANGEW CHEM INT EDIT, V38, P702, DOI 10.1002/(SICI)1521-3773(19990301)38:5<702::AID-ANIE702>3.0.CO
[44]  
2-W
[45]  
KNOLKER HJ, 1992, SYNLETT, P1002
[46]   Amine-Free Reversible Hydrogen Storage in Formate Salts Catalyzed by Ruthenium Pincer Complex without pH Control or Solvent Change [J].
Kothandaraman, Jotheeswari ;
Czaun, Miklos ;
Goeppert, Alain ;
Haiges, Ralf ;
Jones, John-Paul ;
May, Robert B. ;
Prakash, G. K. Surya ;
Olah, George A. .
CHEMSUSCHEM, 2015, 8 (08) :1442-1451
[47]   X-ray Emission Spectroscopy Evidences a Central Carbon in the Nitrogenase Iron-Molybdenum Cofactor [J].
Lancaster, Kyle M. ;
Roemelt, Michael ;
Ettenhuber, Patrick ;
Hu, Yilin ;
Ribbe, Markus W. ;
Neese, Frank ;
Bergmann, Uwe ;
DeBeer, Serena .
SCIENCE, 2011, 334 (6058) :974-977
[48]   Low-Pressure Hydrogenation of Carbon Dioxide Catalyzed by an Iron Pincer Complex Exhibiting Noble Metal Activity [J].
Langer, Robert ;
Diskin-Posner, Yael ;
Leitus, Gregory ;
Shimon, Linda J. W. ;
Ben-David, Yehoshoa ;
Milstein, David .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (42) :9948-9952
[49]   Bioinspired Oxidation Catalysts [J].
Largeron, Martine ;
Fleury, Maurice-Bernard .
SCIENCE, 2013, 339 (6115) :43-44
[50]   Low-Valent Iron Mono-Diazadiene Compounds: Electronic Structure and Catalytic Application [J].
Lichtenberg, Crispin ;
Adelhardt, Mario ;
Gianetti, Thomas L. ;
Meyer, Karsten ;
de Bruin, Bas ;
Gruetzmacher, Hansjoerg .
ACS CATALYSIS, 2015, 5 (10) :6230-6240