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dc.contributor.authorJoost, Maximilian G
dc.contributor.authorNava, Matthew Jordan
dc.contributor.authorTransue, Wesley
dc.contributor.authorCummins, Christopher C
dc.date.accessioned2018-04-13T19:16:19Z
dc.date.available2018-04-13T19:16:19Z
dc.date.issued2017-10
dc.identifier.issn1359-7345
dc.identifier.issn1364-548X
dc.identifier.urihttp://hdl.handle.net/1721.1/114724
dc.description.abstractTargeted as an example of a compound composed of a carbon atom together with two stable neutral leaving groups, 7-isocyano-7-azadibenzonorbornadiene, CN[subscript 2]A (1, A = C[subscript 14]H[subscript 10] or anthracene) has been synthesized and spectroscopically and structurally characterized. The terminal C atom of 1 can be transferred: mesityl nitrile oxide reacts with 1 to produce carbon monoxide, likely via intermediacy of the N-isocyanate OCN[subscript 2]A. Reaction of 1 with [RuCl[subscript 2](CO)(PCy[subscript 3])[subscript 2]] leads to [RuCl2(CO)(1)(PCy3)2] which decomposes unselectively: in the product mixture, the carbide complex [RuCl[subscript 2[](C)(PCy[subscript 3])[subscript 2]] was detected. Upon heating in the solid state or in solution, 1 decomposes to A, N2 and cyanogen (C2N2) as substantiated using molecular beam mass spectrometry, IR and NMR spectroscopy techniques.en_US
dc.description.sponsorshipAlexander von Humboldt Foundation (Feodor Lynen Postdoctoral Fellowship)en_US
dc.language.isoen_US
dc.publisherRoyal Society of Chemistryen_US
dc.relation.isversionofhttp://dx.doi.org/ 10.1039/C7CC06516Gen_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceProf. Cummins via Erja Kajosaloen_US
dc.titleAn exploding N-isocyanide reagent formally composed of anthracene, dinitrogen and a carbon atomen_US
dc.typeArticleen_US
dc.identifier.citationJoost, Maximilian, et al. “An Exploding N-Isocyanide Reagent Formally Composed of Anthracene, Dinitrogen and a Carbon Atom.” Chem. Commun., vol. 53, no. 83, 2017, pp. 11500–03.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.approverCummins, Christopher C.en_US
dc.contributor.mitauthorJoost, Maximilian G
dc.contributor.mitauthorNava, Matthew Jordan
dc.contributor.mitauthorTransue, Wesley
dc.contributor.mitauthorCummins, Christopher C
dc.relation.journalChemical Communicationsen_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.orderedauthorsJoost, Maximilian; Nava, Matthew; Transue, Wesley J.; Cummins, Christopher C.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-9239-7505
dc.identifier.orcidhttps://orcid.org/0000-0001-7445-5663
dc.identifier.orcidhttps://orcid.org/0000-0003-2568-3269
mit.licenseOPEN_ACCESS_POLICYen_US


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