5,11-Dimethyl-6,12-dimethoxyindolo[3,2-b]carbazole

dc.contributor.authorWrobel, Norma
dc.contributor.authorWitulski, Bernhard
dc.contributor.authorSchollmeyer, Dieter
dc.contributor.authorDetert, Heiner
dc.date.accessioned2022-10-04T09:49:25Z
dc.date.available2022-10-04T09:49:25Z
dc.date.issued2013
dc.description.abstractThe title compound, C(22)H(20)N(2)O(2), was prepared in a twofold Cadogan cyclization followed by double N-methyl-ation. The crystal structure is characterized by a zigzag arrangement of centrosymmetric mol-ecules. The indolocarbazole framework is essentially planar [maximum deviation = 0.028 (2) A] and the meth-oxy groups are orthogonal to this plane [C-C-O-C torsion angle = -88.2 (2) degrees ]. The lengths of the C-N bonds are nearly identical and all C-C bonds of the pyrrole subunit are significantly longer than the C-C bonds in the benzene rings.en_GB
dc.description.sponsorshipDFG, Open Access-Publizieren Universität Mainz / Universitätsmedizinde
dc.identifier.doihttp://doi.org/10.25358/openscience-7814
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/7829
dc.language.isoengde
dc.rightsCC-BY-2.0-UK*
dc.rights.urihttps://creativecommons.org/licenses/by/2.0/uk/*
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.title5,11-Dimethyl-6,12-dimethoxyindolo[3,2-b]carbazoleen_GB
dc.typeZeitschriftenaufsatzde
jgu.identifier.pmid23424533
jgu.journal.issue2de
jgu.journal.titleActa crystallographica : Section E, Structure reports onlinede
jgu.journal.volume69de
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.de
jgu.organisation.nameJohannes Gutenberg-Universität Mainz
jgu.organisation.number7950
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.alternativeo255de
jgu.publisher.doi10.1107/S1600536813001463de
jgu.publisher.issn1600-5368de
jgu.publisher.nameMunksgaardde
jgu.publisher.placeCopenhagende
jgu.publisher.urihttp://dx.doi.org/10.1107/S1600536813001463de
jgu.publisher.year2013
jgu.rights.accessrightsopenAccess
jgu.subject.ddccode540de
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTextde
jgu.type.versionPublished versionde
opus.affiliatedSchollmeyer, Dieter
opus.affiliatedDetert, Heiner
opus.date.modified2018-08-02T09:50:20Z
opus.identifier.opusid25264
opus.importsourcepubmed
opus.institute.number0905
opus.metadataonlyfalse
opus.organisation.stringFB 09: Chemie, Pharmazie und Geowissenschaften: Institut für Organische Chemiede_DE
opus.subject.dfgcode00-000
opus.type.contenttypeKeinede_DE
opus.type.contenttypeNoneen_EN

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