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dc.creatorBrito,Iván
dc.creatorLeón,Yasna
dc.creatorArias,Mauricio
dc.creatorVargas,Danitza
dc.creatorCarmona,Francisco
dc.creatorRamírez,Eduardo
dc.creatorRestovic,Ambrosio
dc.creatorCárdenas,Alejandro
dc.creatorWittke,Oscar
dc.creatorLópez-Rodríguez,Matías
dc.date2002-06-01
dc.date.accessioned2020-02-17T15:28:22Z
dc.date.available2020-02-17T15:28:22Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0366-16442002000200012
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/127896
dc.descriptionThe crystal and molecular structure of 5-nitropiridine piperidine-sulfenamide, C10H13N3O2 S is described and compared with other sulfenamides and with other similar compounds. This structure belongs to a type of divalent sulphur compound and crystallizes in the orthorhombic space group Pnma with a= 27.810(4), b=6.797(1), c=6.110(1)Å, and Dx =1.376 g cm-3 with Z=4. The S-N bond distance of 1.699(4) Å is shorter than a single S-N bond [1.74 Å]. The NO2-(C6H3N)-S-N(C 5H10) molecule lies on a crystallographic mirror plane
dc.formattext/html
dc.languageen
dc.publisherSociedad Chilena de Química
dc.relation10.4067/S0366-16442002000200012
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceBoletín de la Sociedad Chilena de Química v.47 n.2 2002
dc.subjectSulfenamides
dc.subjectsulfenic acid derivatives
dc.subjectdivalent sulfur compounds
dc.titleCRYSTAL AND MOLECULAR STRUCTURE OF 5-NITROPIRIDINE PIPERIDINE-SULFENAMIDE


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