Abstract
AbstractAmmonia oxidation catalyzed by molecular compounds is of current interest as a carbon‐free source of dihydrogen. Activation of N−H bonds through coordination to transition metal centers is a key reaction in this process. We report the substantial activation of ammonia via reaction with low‐valent molybdenum complexes of a diborate pentadentate ligand system. Spontaneous loss of dihydrogen from (B2Pz4Py)MoII−NH3 at room temperature to produce the dinuclear μ‐nitrido compound (B2Pz4Py)Mo‐N‐Mo(B2Pz4Py) is observed due to substantial N−H bond weakening upon coordination to Mo. Mechanistic details are supported through the experimental observation/characterization of terminal amido, imido and nitrido complexes and density functional theory computations. The generally under‐appreciated role of bridging nitrido intermediates is revealed and discussed, providing guidance for further catalyst development for this process.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.