6,12-Bis(hexyloxy)-5H,11H-indolo[3,2-b]carbazole
dc.contributor.author | Wrobel, Norma | |
dc.contributor.author | Witulski, Bernhard | |
dc.contributor.author | Schollmeyer, Dieter | |
dc.contributor.author | Detert, Heiner | |
dc.date.accessioned | 2022-06-14T07:08:58Z | |
dc.date.available | 2022-06-14T07:08:58Z | |
dc.date.issued | 2013 | |
dc.description.abstract | The title compound, C30H36N2O2, was prepared in a twofold Cadogan cyclization. The mol-ecule is located about a center of inversion. The indolocarbazole skeleton is essentially planar [maximum deviation = 0.028 (2) A], the C-N bond lengths are nearly identical and the C-C bond lengths of the pyrrole unit are significantly longer than those of the benzene subunits. | en_GB |
dc.description.sponsorship | DFG, Open Access-Publizieren Universität Mainz / Universitätsmedizin | de |
dc.identifier.doi | http://doi.org/10.25358/openscience-7139 | |
dc.identifier.uri | https://openscience.ub.uni-mainz.de/handle/20.500.12030/7153 | |
dc.language.iso | eng | de |
dc.rights | CC-BY-2.0-UK | * |
dc.rights.uri | https://creativecommons.org/licenses/by/2.0/uk/ | * |
dc.subject.ddc | 540 Chemie | de_DE |
dc.subject.ddc | 540 Chemistry and allied sciences | en_GB |
dc.title | 6,12-Bis(hexyloxy)-5H,11H-indolo[3,2-b]carbazole | en_GB |
dc.type | Zeitschriftenaufsatz | de |
jgu.identifier.pmid | 23476379 | |
jgu.journal.issue | 1 | de |
jgu.journal.title | Acta crystallographica : Section E, Structure reports online | de |
jgu.journal.volume | 69 | de |
jgu.organisation.department | FB 09 Chemie, Pharmazie u. Geowissensch. | de |
jgu.organisation.name | Johannes Gutenberg-Universität Mainz | |
jgu.organisation.number | 7950 | |
jgu.organisation.place | Mainz | |
jgu.organisation.ror | https://ror.org/023b0x485 | |
jgu.pages.end | o117 | de |
jgu.pages.start | o116 | de |
jgu.publisher.doi | 10.1107/S1600536812050611 | de |
jgu.publisher.issn | 1600-5368 | de |
jgu.publisher.name | Munksgaard | de |
jgu.publisher.place | Copenhagen | de |
jgu.publisher.uri | http://dx.doi.org/10.1107/S1600536812050611 | de |
jgu.publisher.year | 2013 | |
jgu.rights.accessrights | openAccess | |
jgu.subject.ddccode | 540 | de |
jgu.type.dinitype | Article | en_GB |
jgu.type.resource | Text | de |
jgu.type.version | Published version | de |
opus.affiliated | Schollmeyer, Dieter | |
opus.affiliated | Detert, Heiner | |
opus.date.modified | 2018-08-02T09:52:32Z | |
opus.identifier.opusid | 25265 | |
opus.importsource | pubmed | |
opus.institute.number | 0905 | |
opus.metadataonly | false | |
opus.organisation.string | FB 09: Chemie, Pharmazie und Geowissenschaften: Institut für Organische Chemie | de_DE |
opus.subject.dfgcode | 00-000 | |
opus.type.contenttype | Keine | de_DE |
opus.type.contenttype | None | en_EN |
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