Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9079
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dc.contributor.authorMisra, Rajneeshen_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:30:57Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:30:57Z-
dc.date.issued2018-
dc.identifier.citationSharma, R., Maragani, R., & Misra, R. (2018). C 3-symmetric star shaped donor-acceptor truxenes: Synthesis and photophysical, electrochemical and computational studies. New Journal of Chemistry, 42(2), 882-890. doi:10.1039/c7nj03934den_US
dc.identifier.issn1144-0546-
dc.identifier.otherEID(2-s2.0-85040864688)-
dc.identifier.urihttps://doi.org/10.1039/c7nj03934d-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9079-
dc.description.abstractThis manuscript reports the design and synthesis of C3-symmetric star shaped donor and acceptor substituted truxenes 6, 7, 10 and 11 using Pd-catalyzed Sonogashira cross-coupling and [2+2] cycloaddition-retroelectrocyclization reactions. Their photophysical, electrochemical and computational studies were explored, which indicate strong donor-acceptor interactions and effective tuning of the HOMO-LUMO gap. The computational studies reveal that the TCNE and TCNQ substituted truxenes 10 and 11 exhibit lower HOMO-LUMO gaps compared to truxenes 6 and 7. The reaction pathway of [2+2] cycloaddition-retroelectrocyclization was studied using computational calculations, which reveal that the donor substituted truxene 7 is favourable for cycloaddition-retroelectrocyclization reactions, whereas acceptor substituted truxene 6 is not favourable. © 2018 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.sourceNew Journal of Chemistryen_US
dc.subjectacetic aciden_US
dc.subjectdichloromethaneen_US
dc.subjecthexaneen_US
dc.subjecthydrochloric aciden_US
dc.subjectpalladiumen_US
dc.subjectpolycyclic aromatic hydrocarbonen_US
dc.subjecttetrabutylammoniumen_US
dc.subjecttetracyanoethyleneen_US
dc.subjecttruxeneen_US
dc.subjectunclassified drugen_US
dc.subjectalkylationen_US
dc.subjectArticleen_US
dc.subjectcarbon nuclear magnetic resonanceen_US
dc.subjectcatalysisen_US
dc.subjectchemical phenomenaen_US
dc.subjectconformationen_US
dc.subjectcyclic potentiometryen_US
dc.subjectcyclizationen_US
dc.subjectcycloadditionen_US
dc.subjectdensityen_US
dc.subjectdonor acceptor systemen_US
dc.subjectelectrochemistryen_US
dc.subjectfluorescenceen_US
dc.subjectmass spectrometryen_US
dc.subjectoxidationen_US
dc.subjectoxidation reduction potentialen_US
dc.subjectpriority journalen_US
dc.subjectproton nuclear magnetic resonanceen_US
dc.subjectretroelectrocyclizationen_US
dc.subjectsolubilityen_US
dc.subjectSonogashira reactionen_US
dc.subjectsynthesisen_US
dc.subjectthermogravimetryen_US
dc.subjectthermostabilityen_US
dc.subjectultraviolet spectrophotometryen_US
dc.titleC 3-Symmetric star shaped donor-acceptor truxenes: Synthesis and photophysical, electrochemical and computational studiesen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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