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dc.contributor.authorMartin-Drumel, Marie-Aline
dc.contributor.authorLopez, Christopher A.
dc.contributor.authorCrabtree, Kyle N.
dc.contributor.authorNguyen, Thanh L.
dc.contributor.authorThorwirth, Sven
dc.contributor.authorStanton, John F.
dc.contributor.authorMcCarthy, Michael C.
dc.contributor.authorNava, Matthew Jordan
dc.contributor.authorWomack, Caroline C.
dc.contributor.authorCummins, Christopher C
dc.date.accessioned2018-07-12T15:21:48Z
dc.date.available2018-07-12T15:21:48Z
dc.date.issued2016-08
dc.identifier.issn0002-7863
dc.identifier.issn1520-5126
dc.identifier.urihttp://hdl.handle.net/1721.1/116934
dc.description.abstractThionitrous acid (HSNO), a potential key intermediate in biological signaling pathways, has been proposed to link NO and H[superscript 2]S biochemistries, but its existence and stability in vivo remain controversial. We establish that HSNO is spontaneously formed in high concentration when NO and H[subscript 2]S gases are mixed at room temperature in the presence of metallic surfaces. Our measurements reveal that HSNO is formed by the reaction H[superscript 2]S + N[subscript 2]O[subscript 3] → HSNO + HNO[subscript 2], where N[superscript 2]O[superscript 3] is a product of NO disproportionation. These studies also suggest that further reaction of HSNO with H[subscript 2]S may form HNO and HSSH. The length of the S–N bond has been derived to high precision and is found to be unusually long: 1.84 Å, the longest S–N bond reported to date for an R-SNO compound. The present structural and, particularly, reactivity investigations of this elusive molecule provide a firm foundation to better understand its potential physiological chemistry and propensity to undergo S–N bond cleavage in vivo.en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/jacs.6b05886en_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.sourceOther repositoryen_US
dc.titleSpontaneous and Selective Formation of HSNO, a Crucial Intermediate Linking Hen_US
dc.typeArticleen_US
dc.identifier.citationNava, Matthew, et al. “Spontaneous and Selective Formation of HSNO, a Crucial Intermediate Linking H 2 S and Nitroso Chemistries.” Journal of the American Chemical Society, vol. 138, no. 36, Sept. 2016, pp. 11441–44. © 2016 American Chemical Societyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorNava, Matthew Jordan
dc.contributor.mitauthorWomack, Caroline C.
dc.contributor.mitauthorCummins, Christopher C
dc.relation.journalJournal of the American Chemical Societyen_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.orderedauthorsNava, Matthew; Martin-Drumel, Marie-Aline; Lopez, Christopher A.; Crabtree, Kyle N.; Womack, Caroline C.; Nguyen, Thanh L.; Thorwirth, Sven; Cummins, Christopher C.; Stanton, John F.; McCarthy, Michael C.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-9239-7505
dc.identifier.orcidhttps://orcid.org/0000-0003-2568-3269
mit.licensePUBLISHER_POLICYen_US


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