5-[(4-Methyl­phen­yl)sulfon­yl]-1-phenyl­thio­pyrano[4,3-b]indole-3(5H)-thione di­chloro­methane monosolvate

dc.contributor.authorDassonneville, Benjamin
dc.contributor.authorSchollmeyer, Dieter
dc.contributor.authorDetert, Heiner
dc.date.accessioned2025-12-01T10:08:46Z
dc.date.issued2023
dc.description.abstractRhodium-catalyzed [2+2+2] cyclo­addition of carbon di­sulfide to o,N-dialkynyl­tosyl­anilines gives two isomeric indolo­thio­pyran­thio­nes, a violet and a red isomer. This is the first crystal structure of a red isomer, which crystallizes with one solvent mol­ecule of di­chloro­methane in the asymmetric unit, C24H17NO2S3·CH2Cl2. In the extended structure, centrosymmetric pairs of the planar annulated system are arranged in strands and solvent mol­ecules fill the space between the strands.en
dc.identifier.doihttps://doi.org/10.25358/openscience-13739
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/13760
dc.language.isoeng
dc.rightsCC-BY-4.0
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddc540 Chemiede
dc.subject.ddc540 Chemistry and allied sciencesen
dc.title5-[(4-Methyl­phen­yl)sulfon­yl]-1-phenyl­thio­pyrano[4,3-b]indole-3(5H)-thione di­chloro­methane monosolvateen
dc.typeZeitschriftenaufsatz
elements.depositor.primary-group-descriptorFachbereich Chemie, Pharmazie und Geowissenschaften
elements.object.id291904
elements.object.labelsannulated heterocycles
elements.object.labelscrystal structure
elements.object.labelssulfur
elements.object.labels3402 Inorganic chemistry
elements.object.typejournal-article
jgu.identifier.uuid3a39fbef-7c32-47a6-acc1-99d47ac3a747
jgu.journal.issue5
jgu.journal.titleIUCrData
jgu.journal.volume8
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.
jgu.organisation.nameJohannes Gutenberg-Universität Mainz
jgu.organisation.number7950
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.alternativex230354
jgu.publisher.doi10.1107/s2414314623003541
jgu.publisher.eissn2414-3146
jgu.publisher.licenceCC BY
jgu.publisher.nameIUCr
jgu.publisher.placeChester
jgu.publisher.year2023
jgu.rights.accessrightsopenAccess
jgu.subject.ddccode540
jgu.subject.dfgNaturwissenschaften
jgu.type.dinitypeArticleen_GB
jgu.type.resourceText
jgu.type.versionPublished version

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