Publication:
Dibenzopleiadiene-embeded polyaromatics: Via [4 + 3] annulative decarbonylation/decarboxylation

dc.contributor.authorKritchasorn Kantaroden_US
dc.contributor.authorThanapat Worakulen_US
dc.contributor.authorDarunee Soorukramen_US
dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorPanida Surawatanawongen_US
dc.contributor.authorWorawat Wattanathanaen_US
dc.contributor.authorPawaret Leowanawaten_US
dc.contributor.otherKasetsart Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2022-08-04T08:24:48Z
dc.date.available2022-08-04T08:24:48Z
dc.date.issued2021-02-07en_US
dc.description.abstractA novel strategy is developed for the synthesis of dibenzopleiadiene-embedded polycyclic aromatic hydrocarbons from 1,8-naphthalic anhydride derivatives and cyclic diaryliodonium salts through a palladium-catalyzed cascade [4 + 3] decarbonylative/decarboxylative annulation. The mechanism of the reaction is proposed and the molecular structure, photophysical properties, and frontier molecular orbitals of diverse dibenzopleiadiene-embedded polyaromatics are elucidated by X-ray crystallography, UV-Vis and fluorescence spectroscopy, and DFT calculations.en_US
dc.identifier.citationOrganic Chemistry Frontiers. Vol.8, No.3 (2021), 522-530en_US
dc.identifier.doi10.1039/d0qo00942cen_US
dc.identifier.issn20524129en_US
dc.identifier.issn20524110en_US
dc.identifier.other2-s2.0-85100736380en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/76621
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85100736380&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleDibenzopleiadiene-embeded polyaromatics: Via [4 + 3] annulative decarbonylation/decarboxylationen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85100736380&origin=inwarden_US

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