| dc.contributor.author | Smith, Stacey J. | |
| dc.contributor.author | Jamison, Timothy F. | |
| dc.contributor.author | Standley, Eric | |
| dc.contributor.author | Mueller, Peter | |
| dc.date.accessioned | 2015-06-22T13:57:09Z | |
| dc.date.available | 2015-06-22T13:57:09Z | |
| dc.date.issued | 2014-04 | |
| dc.date.submitted | 2014-02 | |
| dc.identifier.issn | 0276-7333 | |
| dc.identifier.issn | 1520-6041 | |
| dc.identifier.uri | http://hdl.handle.net/1721.1/97490 | |
| dc.description.abstract | A series of air-stable nickel complexes of the form L[subscript 2]Ni(aryl) X (L = monodentate phosphine, X = Cl, Br) and LNi(aryl)X (L = bis-phosphine) have been synthesized and are presented as a library of precatalysts suitable for a wide variety of nickel-catalyzed transformations. These complexes are easily synthesized from low-cost NiCl[subscript 2]·6H[subscript 2]O or NiBr[subscript 2]·3H[subscript 2]O and the desired ligand followed by addition of 1 equiv of Grignard reagent. A selection of these complexes were characterized by single-crystal X-ray diffraction, and an analysis of their structural features is provided. A case study of their use as precatalysts for the nickel-catalyzed carbonyl-ene reaction is presented, showing superior reactivity in comparison to reactions using Ni(cod)[subscript 2]. Furthermore, as the precatalysts are all stable to air, no glovebox or inert-atmosphere techniques are required to make use of these complexes for nickel-catalyzed reactions. | en_US |
| dc.description.sponsorship | National Institute of General Medical Sciences (U.S.) (GM63755) | en_US |
| dc.description.sponsorship | National Science Foundation (U.S.). Graduate Research Fellowship | en_US |
| dc.language.iso | en_US | |
| dc.publisher | American Chemical Society (ACS) | en_US |
| dc.relation.isversionof | http://dx.doi.org/10.1021/om500156q | 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 | American Chemical Society | en_US |
| dc.title | A Broadly Applicable Strategy for Entry into Homogeneous Nickel(0) Catalysts from Air-Stable Nickel(II) Complexes | en_US |
| dc.type | Article | en_US |
| dc.identifier.citation | Standley, Eric A., Stacey J. Smith, Peter Müller, and Timothy F. Jamison. “A Broadly Applicable Strategy for Entry into Homogeneous Nickel(0) Catalysts from Air-Stable Nickel(II) Complexes.” Organometallics 33, no. 8 (April 28, 2014): 2012–2018. © 2014 American Chemical Society | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Chemistry | en_US |
| dc.contributor.mitauthor | Standley, Eric | en_US |
| dc.contributor.mitauthor | Smith, Stacey J. | en_US |
| dc.contributor.mitauthor | Mueller, Peter | en_US |
| dc.contributor.mitauthor | Jamison, Timothy F. | en_US |
| dc.relation.journal | Organometallics | en_US |
| dc.eprint.version | Final published version | 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 | Standley, Eric A.; Smith, Stacey J.; Müller, Peter; Jamison, Timothy F. | en_US |
| dc.identifier.orcid | https://orcid.org/0000-0002-8601-7799 | |
| mit.license | PUBLISHER_POLICY | en_US |
| mit.metadata.status | Complete | |