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dc.contributor.authorSues, Peter V. E.
dc.contributor.authorJohn, Jeremy M
dc.contributor.authorSchrock, Richard Royce
dc.contributor.authorMueller, Peter
dc.date.accessioned2017-04-20T15:22:17Z
dc.date.available2017-04-20T15:22:17Z
dc.date.issued2016-02
dc.date.submitted2016-01
dc.identifier.issn0276-7333
dc.identifier.issn1520-6041
dc.identifier.urihttp://hdl.handle.net/1721.1/108288
dc.description.abstractMolybdenum imido alkylidene and tungsten oxo alkylidene complexes that contain a tridentate “pincer” [ONO]²⁻ ligand have been prepared and treated with ethylene to give unsubstituted metallacyclobutane complexes that have a 16e count. Both Mo and W metallacyclobutane complexes exchange C₂D₄ into the metallacyclobutane ring at 22 °C at a rate that is first order in metal and zero order in C₂D₄. These metallacycles lose ethylene at least 10⁴–10⁵ times slower than reported 14e unsubstituted Mo and W metallacyclobutane complexes that have been explored in the literature that have a TBP geometry with the metallacyclobutane ring bound in the equatorial positions. Our studies suggest that breaking up the metallacyclobutane ring in these 16e d⁰ Mo or W complexes is slow because a 14e TBP metallacyclobutane complex cannot be accessed readily.en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (CHE-1205189)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (CHE-0946721)en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://pubs.acs.org/doi/abs/10.1021/acs.organomet.5b00976en_US
dc.sourceProf. Schrocken_US
dc.titleMolybdenum and Tungsten Alkylidene and Metallacyclobutane Complexes That Contain a Dianionic Biphenolate Pincer Liganden_US
dc.typeArticleen_US
dc.identifier.citationSues, Peter E.; John, Jeremy M.; Schrock, Richard R. and Müller, Peter. “Molybdenum and Tungsten Alkylidene and Metallacyclobutane Complexes That Contain a Dianionic Biphenolate Pincer Ligand.” Organometallics 35, no. 5 (March 2016): 758–761. © 2016 American Chemical Societyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.approverSchrock, Richard Royceen_US
dc.contributor.mitauthorSues, Peter V. E.
dc.contributor.mitauthorJohn, Jeremy M
dc.contributor.mitauthorSchrock, Richard Royce
dc.contributor.mitauthorMueller, Peter
dc.relation.journalOrganometallicsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsSues, Peter E.; John, Jeremy M.; Schrock, Richard R.; Müller, Peteren_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-3975-119X
dc.identifier.orcidhttps://orcid.org/0000-0002-7405-6811
dc.identifier.orcidhttps://orcid.org/0000-0001-5827-3552
mit.licensePUBLISHER_POLICYen_US


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