A Stable Six‐Coordinate Intermediate in Ammonia–Dinitrogen Exchange at Schrock's Molybdenum Catalyst
- 4 May 2009
- journal article
- research article
- Published by Wiley in Chemistry – A European Journal
- Vol. 15 (20) , 5073-5082
Abstract
Juggling N2 and NH3: Exchange of ammonia by dinitrogen at Schrock's five‐coordinate dinitrogen‐fixating molybdenum catalyst is likely to involve stable six‐coordinate intermediates (see figure). magnified image In this work, we investigate the mechanism of the ammonia–dinitrogen exchange reaction, which is the decisive step to close the catalytic cycle of Schrock's dinitrogen reduction sequence under ambient conditions. We identify several viable pathways for the approach of dinitrogen to the five‐coordinate molybdenum center of the ammonia complex by means of first‐principles molecular‐dynamics simulations. These exploratory simulations are then complemented by rigorous quantum‐chemical structure optimizations. Our calculations have been performed for the full Schrock catalyst without simplifying the large chelate ligand, and are hence not affected by model assumptions. We show that the reaction obeys an addition–elimination mechanism via a stable six‐coordinate intermediate. This intermediate has been fully characterized by stationary quantum‐chemical methods. The predicted infrared spectrum of this species features an NN stretching vibration, which is well separated in frequency from all other NN stretching vibrations of N2‐binding complexes involved in the Schrock cycle. Depending on the life time of this intermediate in the reaction liquor, the production of this intermediate might even be monitored by the absorption of the NN stretching vibration.Keywords
This publication has 71 references indexed in Scilit:
- Catalytic reduction of dinitrogen to ammonia at a single molybdenum centerProceedings of the National Academy of Sciences, 2006
- Reduction of dinitrogenProceedings of the National Academy of Sciences, 2006
- Synthesis of Molybdenum Complexes that Contain “Hybrid” Triamidoamine Ligands, [(Hexaisopropylterphenyl-NCH2CH2)2NCH2CH2N-aryl]3-, and Studies Relevant to Catalytic Reduction of DinitrogenInorganic Chemistry, 2006
- Energetik und Mechanismus einer katalytischen Ammoniaksynthese bei Raumtemperatur (Schrock‐Zyklus); Vergleich mit der biologischen Stickstoff‐FixierungAngewandte Chemie, 2005
- Estimation of the Vibrational Contribution to the Entropy Change Associated with the Low- to High-Spin Transition in Fe(phen)2(NCS)2 Complexes: Results Obtained by IR and Raman Spectroscopy and DFT CalculationsThe Journal of Physical Chemistry A, 2002
- High performance computational chemistry: An overview of NWChem a distributed parallel applicationComputer Physics Communications, 2000
- Functional analogs for the reduction of certain nitrogenase substrates. Are multiple sites within the Fe/Mo/S active center involved in the 6e– reduction of N2?JBIC Journal of Biological Inorganic Chemistry, 1996
- Elementary reactions, structure-function relationships, and the potential relevance of low molecular weight metal-sulfur ligand complexes to biological N2 fixationJBIC Journal of Biological Inorganic Chemistry, 1996
- Nitrogenase: substrate binding and activationJBIC Journal of Biological Inorganic Chemistry, 1996
- Energy-adjustedab initio pseudopotentials for the second and third row transition elementsTheoretical Chemistry Accounts, 1990