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dc.contributor.authorCossairt, Brandi M.
dc.contributor.authorCummins, Christopher C.
dc.date.accessioned2011-12-14T14:27:46Z
dc.date.available2011-12-14T14:27:46Z
dc.date.issued2010-04
dc.date.submitted2010-02
dc.identifier.issn1144-0546
dc.identifier.urihttp://hdl.handle.net/1721.1/67661
dc.description.abstractA reaction scheme has been devised according to 3 RX + 3 Ti(III) + 0.25 P₄ → PR₃ + 3 XTi(IV), wherein RX = PhBr, CyBr, Me₃SiI or Ph₃SnCl, with contrasting results in the case of more hindered RX. The scheme accomplishes the direct radical functionalization of white phosphorus without the intermediacy of PCl₃.en_US
dc.language.isoen_US
dc.publisherRSC Publishingen_US
dc.relation.isversionofhttp://dx.doi.org/10.1039/c0nj00124den_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourceProf. Cumminsen_US
dc.titleRadical synthesis of trialkyl, triaryl, trisilyl and tristannyl phosphines from P₄en_US
dc.typeArticleen_US
dc.identifier.citationCossairt, Brandi M., and Christopher C. Cummins. “Radical Synthesis of Trialkyl, Triaryl, Trisilyl and Tristannyl Phosphines from P4.” New Journal of Chemistry 34.8 (2010) : 1533.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.approverCummins, Christopher C.
dc.contributor.mitauthorCummins, Christopher C.
dc.contributor.mitauthorCossairt, Brandi M.
dc.relation.journalNew Journal of Chemistryen_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.orderedauthorsCossairt, Brandi M.; Cummins, Christopher C.en
dc.identifier.orcidhttps://orcid.org/0000-0003-2568-3269
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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