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dc.contributor.authorMartin-Drumel, Marie-Aline
dc.contributor.authorMcCarthy, Michael C.
dc.contributor.authorPatterson, David
dc.contributor.authorJoost, Maximilian G
dc.contributor.authorNava, Matthew Jordan
dc.contributor.authorTransue, Wesley
dc.contributor.authorCummins, Christopher C
dc.date.accessioned2019-02-27T17:01:51Z
dc.date.available2019-02-27T17:01:51Z
dc.date.issued2018-05
dc.date.submitted2018-03
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttp://hdl.handle.net/1721.1/120567
dc.description.abstractSulfur monoxide (SO) is a highly reactive molecule and thus, eludes bulk isolation. We report here on synthesis and reactivity of a molecular precursor for SO generation, namely 7-sulfin-ylamino-7-azadibenzonorbornadiene (1). This compound has been shown to fragment readily driven by dinitrogen expulsion and anthracene formation on heating in the solid state and in solution, releasing SO at mild temperatures (<100 ◦C). The generated SO was detected in the gas phase by MS and rotational spectroscopy. In solution, 1 allows for SO transfer to organic molecules as well as transition metal complexes. Keywords: microwave spectroscopy; reactive intermediate; molecular precursor; astrochemistry; sulfur monoxideen_US
dc.publisherNational Academy of Sciences (U.S.)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/PNAS.1804035115en_US
dc.rightsArticle 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.sourcePNASen_US
dc.titleSulfur monoxide thermal release from an anthracene-based precursor, spectroscopic identification, and transfer reactivityen_US
dc.typeArticleen_US
dc.identifier.citationJoost, Maximilian et al. “Sulfur Monoxide Thermal Release from an Anthracene-Based Precursor, Spectroscopic Identification, and Transfer Reactivity.” Proceedings of the National Academy of Sciences 115, 23 (May 2018): 5866–5871 © National Academy of Sciencesen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorJoost, Maximilian G
dc.contributor.mitauthorNava, Matthew Jordan
dc.contributor.mitauthorTransue, Wesley
dc.contributor.mitauthorCummins, Christopher C
dc.relation.journalProceedings of the National Academy of Sciencesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2019-02-08T14:37:04Z
dspace.orderedauthorsJoost, Maximilian; Nava, Matthew; Transue, Wesley J.; Martin-Drumel, Marie-Aline; McCarthy, Michael C.; Patterson, David; 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.licensePUBLISHER_POLICYen_US


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