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dc.rights.licenseopenen_US
dc.contributor.authorOLIVIER, Celine
dc.contributor.authorNAGATOMO, Nao
dc.contributor.authorMORI, Tadashi
dc.contributor.authorMCCLENAGHAN, Nathan
dc.contributor.authorJONUSAUSKAS, Gediminas
dc.contributor.authorKAUFFMANN, Brice
dc.contributor.authorKUWAHARA, Yutaka
dc.contributor.authorTAKAFUJI, Makoto
dc.contributor.authorIHARA, Hirotaka
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
dc.contributor.authorFERRAND, Yann
dc.date.accessioned2023-03-28T08:01:00Z
dc.date.available2023-03-28T08:01:00Z
dc.date.issued2022-12-13
dc.identifier.issn2052-4129en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/172635
dc.description.abstractEnThe synthesis and characterization of an original π-extended cationic azahelicene is reported. The phenanthrene-fused aza[7]helicene derivative encompasses a total of ten aromatic fused rings leading to a dissymmetric yet helically folded structure, as revealed by NMR and X-ray diffraction analyses. The polyaromatic and cationic nature of the new azahelicenium makes it soluble in both organic and aqueous media, which allowed photophysical studies in solvents of different polarities. The extended chromophoric species demonstrates a broad absorption over the whole visible range and orange-red fluorescence emission. Chiral resolution of the racemate was performed subsequently, affording two optically pure and configurationally stable azahelicenium enantiomers. Multi-band circular dichroism and long-wavelength circularly polarized emission were observed, associated with remarkable absorption and luminescence dissymmetry factors, both in organic and aqueous media.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/us/*
dc.title.enA π-extended phenanthrene-fused aza[7]helicenium as a novel chiroptically-active architecture in organic and aqueous media
dc.title.alternativeOrg. Chem. Front.en_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1039/D2QO01942Fen_US
dc.subject.halChimie/Matériauxen_US
dc.description.sponsorshipEuropeProgram Initiative d’Excellenceen_US
bordeaux.journalOrganic Chemistry Frontiersen_US
bordeaux.page752-758en_US
bordeaux.volume10en_US
bordeaux.hal.laboratoriesCBMN : Chimie & de Biologie des Membranes & des Nano-objets - UMR 5248en_US
bordeaux.issue3en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-04048641
hal.version1
hal.date.transferred2023-03-28T08:01:10Z
hal.exporttrue
dc.rights.ccCC BY-NCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Organic%20Chemistry%20Frontiers&rft.date=2022-12-13&rft.volume=10&rft.issue=3&rft.spage=752-758&rft.epage=752-758&rft.eissn=2052-4129&rft.issn=2052-4129&rft.au=OLIVIER,%20Celine&NAGATOMO,%20Nao&MORI,%20Tadashi&MCCLENAGHAN,%20Nathan&JONUSAUSKAS,%20Gediminas&rft.genre=article


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