dc.contributor.author | Wickramasinghe Weerakkodi Appuhamilage, Lasantha A | |
dc.contributor.author | Ogawa, Takaya | |
dc.contributor.author | Schrock, Richard Royce | |
dc.contributor.author | Miller, Peter G | |
dc.date.accessioned | 2018-06-25T17:32:48Z | |
dc.date.available | 2018-06-25T17:32:48Z | |
dc.date.issued | 2017-06 | |
dc.date.submitted | 2017-05 | |
dc.identifier.issn | 0002-7863 | |
dc.identifier.issn | 1520-5126 | |
dc.identifier.uri | http://hdl.handle.net/1721.1/116567 | |
dc.description.abstract | [Ar₂N₃]Mo(N)(O-t-Bu), which contains the conformationally rigid pyridine-based diamido ligand, [2,6-(ArNCH₂)₂NC₅H₃]²– (Ar = 2,6-diisopropylphenyl), can be prepared from H₂[Ar₂N₃], butyllithium, and (t-BuO)₃Mo(N). [Ar₂N₃]Mo(N)(O-t-Bu) serves as a catalyst or precursor for the catalytic reduction of molecular nitrogen to ammonia in diethyl ether between −78 and 22 °C in a batchwise manner with CoCp*₂ as the electron source and Ph₂NH₂OTf as the proton source. Up to ∼10 equiv of ammonia can be formed per Mo with a maximum efficiency in electrons of ∼43%. | en_US |
dc.description.sponsorship | United States. Department of Energy (Award DE-SC0013307) | en_US |
dc.description.sponsorship | National Science Foundation (U.S.) (Grant CHE- 0946721) | en_US |
dc.language.iso | en_US | |
dc.publisher | American Chemical Society (ACS) | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1021/jacs.7b04800 | en_US |
dc.rights | Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. | en_US |
dc.source | Prof. Schrock via Erja Kajosalo | en_US |
dc.title | Reduction of Dinitrogen to Ammonia Catalyzed by Molybdenum Diamido Complexes | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Wickramasinghe, Lasantha A. et al. “Reduction of Dinitrogen to Ammonia Catalyzed by Molybdenum Diamido Complexes.” Journal of the American Chemical Society 139, 27 (June 2017): 9132–9135 © 2017 American Chemical Society | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Chemistry | en_US |
dc.contributor.approver | Schrock, Richard Royce | en_US |
dc.contributor.mitauthor | Wickramasinghe Weerakkodi Appuhamilage, Lasantha A | |
dc.contributor.mitauthor | Ogawa, Takaya | |
dc.contributor.mitauthor | Schrock, Richard Royce | |
dc.contributor.mitauthor | Miller, Peter G | |
dc.relation.journal | Journal of the American Chemical Society | en_US |
dc.eprint.version | Author's final manuscript | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dspace.orderedauthors | Wickramasinghe, Lasantha A.; Ogawa, Takaya; Schrock, Richard R.; Müller, Peter | en_US |
dspace.embargo.terms | N | en_US |
dc.identifier.orcid | https://orcid.org/0000-0003-2933-8665 | |
dc.identifier.orcid | https://orcid.org/0000-0003-1654-1146 | |
dc.identifier.orcid | https://orcid.org/0000-0001-5827-3552 | |
mit.license | PUBLISHER_POLICY | en_US |