Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-7760
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dc.contributor.authorResch, Sebastian-
dc.contributor.authorQuell, Thomas-
dc.contributor.authorSchollmeyer, Dieter-
dc.contributor.authorWaldvogel, Siegfried R.-
dc.date.accessioned2022-09-14T08:30:10Z-
dc.date.available2022-09-14T08:30:10Z-
dc.date.issued2015-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/7775-
dc.description.abstractThe hetero­tetra­cene skeleton of the title mol­ecule, C23H14Br2N2OS, is defined by linear annulation of four six-membered rings, including two N heteroatoms. This moiety is nearly planar (r.m.s. deviation = 0.055 Å), with a slight twist of 4.1 (2)° between the two halves of the aromatic system. The dihedral angle between the least-squares plane of the skeleton and the benzyl group is 24.5 (3)°; the C-S-C angle involving the benzyl­sulfanyl group is 99.2 (4)°. In the crystal, mol­ecules are [pi]-stacked in an anti­parallel fashion along [110], with a distance between the aromatic planes of 3.47 (2) Å. Inter­molecular N-H...O hydrogen bonds form chains extending parallel to [001] and bridge the anti­parallel inter­digitated stacks of mol­ecules.en_GB
dc.description.sponsorshipDFG, Open Access-Publizieren Universität Mainz / Universitätsmedizinde
dc.language.isoengde
dc.rightsCC BY*
dc.rights.urihttps://creativecommons.org/licenses/by/2.0/uk*
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.titleCrystal structure of 12-benzyl­sulfanyl-2,9-di­bromo-6H-dibenzo[b,g][1,8]naphthyridin-11-oneen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-7760-
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.de
jgu.organisation.number7950-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleActa crystallographica : Section E, Structure reports onlinede
jgu.journal.volume71de
jgu.journal.issue9de
jgu.pages.starto675de
jgu.pages.endo676de
jgu.publisher.year2015-
jgu.publisher.nameWiley-Blackwellde
jgu.publisher.placeOxfordde
jgu.publisher.urihttp://dx.doi.org/10.1107/S2056989015014541de
jgu.organisation.placeMainz-
jgu.subject.ddccode540de
opus.date.modified2018-09-05T09:11:36Z-
opus.subject.dfgcode00-000-
opus.organisation.stringFB 09: Chemie, Pharmazie und Geowissenschaften: Institut für Organische Chemiede_DE
opus.identifier.opusid51964-
opus.institute.number0905-
opus.metadataonlyfalse-
opus.type.contenttypeKeinede_DE
opus.type.contenttypeNoneen_EN
opus.affiliatedSchollmeyer, Dieter-
opus.affiliatedWaldvogel, Siegfried-
jgu.publisher.doi10.1107/S2056989015014541de
jgu.organisation.rorhttps://ror.org/023b0x485-
Appears in collections:DFG-OA-Publizieren (2012 - 2017)

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