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      Unique behaviour of dinitrogen-bridged dimolybdenum complexes bearing pincer ligand towards catalytic formation of ammonia

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          Abstract

          It is vital to design effective nitrogen fixation systems that operate under mild conditions, and to this end we recently reported an example of the catalytic formation of ammonia using a dinitrogen-bridged dimolybdenum complex bearing a pincer ligand, where up to twenty three equivalents of ammonia were produced based on the catalyst. Here we study the origin of the catalytic behaviour of the dinitrogen-bridged dimolybdenum complex bearing the pincer ligand with density functional theory calculations, based on stoichiometric and catalytic formation of ammonia from molecular dinitrogen under ambient conditions. Comparison of di- and mono-molybdenum systems shows that the dinitrogen-bridged dimolybdenum core structure plays a critical role in the protonation of the coordinated molecular dinitrogen in the catalytic cycle.

          Abstract

          Research into molecular catalysts for conversion of nitrogen into ammonia under mild conditions is ongoing. Here, the authors synthesize a dimolybdenum–nitride complex and verify the role of the dimetallic core in the protonation of the coordinated dinitrogen.

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          Most cited references29

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          Catalytic reduction of dinitrogen to ammonia at a single molybdenum center.

          Dinitrogen (N2) was reduced to ammonia at room temperature and 1 atmosphere with molybdenum catalysts that contain tetradentate [HIPTN3N]3- triamidoamine ligands (such as [HIPTN3N]Mo(N2), where [HIPTN3N]3- is [(3,5-(2,4,6-i-Pr3C6H2)2C6H3NCH2CH2)3N]3-) in heptane. Slow addition of the proton source [(2,6-lutidinium)(BAr'4), where Ar' is 3,5-(CF3)2C6H3]and reductant (decamethyl chromocene) was critical for achieving high efficiency ( approximately 66% in four turnovers). Numerous x-ray studies, along with isolation and characterization of six proposed intermediates in the catalytic reaction under noncatalytic conditions, suggest that N2 was reduced at a sterically protected, single molybdenum center that cycled from Mo(III) through Mo(VI) states.
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            Catalytic conversion of nitrogen to ammonia by a molecular Fe model complex

            The reduction of N2 to NH3 is a requisite transformation for life. 1 While it is widely appreciated that the iron-rich cofactors of nitrogenase enzymes facilitate this transformation, 2-5 how they do so remains poorly understood. A central element of debate has been the exact site(s) of nitrogen coordination and reduction. 6,7 The synthetic inorganic community placed an early emphasis on Mo 8 , because Mo was thought to be an essential element of nitrogenases 3 and because pioneering work by Chatt and coworkers established that well-defined Mo model complexes could mediate the stoichiometric conversion of N2 to NH3. 9 This chemical transformation can be performed in a catalytic fashion by two well-defined molecular systems that feature Mo centres. 10,11 However, it is now thought that Fe is the only transition metal essential to all nitrogenases, 3 and recent biochemical and spectroscopic data has implicated Fe instead of Mo as the site of N2 binding in the FeMo-cofactor. 12 In this work, we describe a tris(phosphine)borane-supported Fe complex that catalyzes the reduction of N2 to NH3 under mild conditions, wherein >40% of the H+/e- equivalents are delivered to N2. Our results indicate that a single Fe site may be capable of stabilizing the various NxHy intermediates generated en route to catalytic NH3 formation. Geometric tunability at Fe imparted by a flexible Fe-B interaction in our model system appears to be important for efficient catalysis. 13-15 We propose that the interstitial light C-atom recently assigned in the nitrogenase cofactor may play a similar role, 16,17 perhaps by enabling a single Fe site to mediate the enzymatic catalysis via a flexible Fe-C interaction. 18
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              Mechanistic aspects of dinitrogen cleavage and hydrogenation to produce ammonia in catalysis and organometallic chemistry: relevance of metal hydride bonds and dihydrogen.

              Dinitrogen cleavage and hydrogenation by transition-metal centers to produce ammonia is central in industry and in Nature. After an introductory section on the thermodynamic and kinetic challenges linked to N2 splitting, this tutorial review discusses three major classes of transition-metal systems (homogeneous, heterogeneous and biological) capable of achieving dissociation and hydrogenation of dinitrogen. Molecular complexes, solid-state Haber-Bosch catalytic systems, silica-supported tantalum hydrides and nitrogenase will be discussed. Emphasis is focused on the reaction mechanisms operating in the process of dissociation and hydrogenation of dinitrogen, and in particular on the key role played by metal hydride bonds and by dihydrogen in such reactions.
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                Author and article information

                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Pub. Group
                2041-1723
                28 April 2014
                : 5
                : 3737
                Affiliations
                [1 ]Institute for Materials Chemistry and Engineering and International Research Center for Molecular Systems, Kyushu University, Nishi-ku , Fukuoka 819-0395, Japan
                [2 ]Elements Strategy Initiative for Catalysts and Batteries (ESICB), Kyoto University, Nishikyo-ku , Kyoto 615-8520, Japan
                [3 ]Institute of Engineering Innovation, School of Engineering, The University of Tokyo, Yayoi, Bunkyo-ku , Tokyo 113-8656, Japan
                [4 ]These authors contributed equally to this work
                Author notes
                Article
                ncomms4737
                10.1038/ncomms4737
                4015321
                24769530
                54b42426-ed8c-4c9f-9b55-3b3733ea2c4d
                Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.

                This work is licensed under a Creative Commons Attribution 3.0 Unported License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/

                History
                : 06 January 2014
                : 27 March 2014
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