Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/8761
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dc.contributor.authorPopli, Charuen_US
dc.contributor.authorPatil, Yuvrajen_US
dc.contributor.authorMisra, Rajneeshen_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:29:43Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:29:43Z-
dc.date.issued2020-
dc.identifier.citationPopli, C., Jang, Y., Patil, Y., Misra, R., & D'Souza, F. (2020). Formation of highly efficient, long-lived charge separated states in star-shaped ferrocene-diketopyrrolopyrrole-triphenylamine Donor–Acceptor–Donor conjugates. Chemistry - A European Journal, 26(66), 15109-15115. doi:10.1002/chem.202002851en_US
dc.identifier.issn0947-6539-
dc.identifier.otherEID(2-s2.0-85092558707)-
dc.identifier.urihttps://doi.org/10.1002/chem.202002851-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/8761-
dc.description.abstractThe significance of multiple number of donor–acceptor entities on a central electron donor in a star-shaped molecular system in improving light energy harvesting ability is reported. For this, donor–acceptor–donor type conjugates comprised up to three entities ferrocenyl (Fc)-diketopyrrolopyrrole (DPP) onto a central triphenylamine (TPA), (4–6) by the Pd-catalyzed Sonogashira cross-coupling reactions have been newly synthesized and characterized. Donor–acceptor conjugates possessing diketopyrrolopyrrole (1 to 3 entities) onto the central triphenylamine, (1–3) served as reference dyads while monomeric DPP and Fc-DPP served as control compounds. Both DPP and Fc-DPP carrying conjugates exhibited red-shifted absorption compared to their respective control compounds revealing existence of ground state interactions. Furthermore, DPP fluorescence in 4–6 was found to be quantitatively quenched while for 1–3, this property varied between 73–65 % suggesting occurrence moderate amounts of excited state events. The electrochemical investigations exhibited an additional low potential oxidation in the case of Fc-DPP-TPA based derivatives (4–6) owing to the presence of ferrocene unit(s). This was in addition to DPP and TPA redox peaks. Using spectral, electrochemical and computational studies, Gibbs free-energy calculations were performed to visualize excited state charge separation (ΔGCS) in these donor–acceptor conjugates as a function of different number of Fc-DPP entities. Formation of Fc+-DPP.−-TPA charge separated states (CSS) in the case of 4–6 was evident. Using spectroelectrochemical studies, spectrum of CSS was deduced. Finally, femtosecond transient absorption spectral studies were performed to gather information on excited state charge separation. Increasing the number of Fc-DPP entities in 4–6 improved charge separation rates. Surprisingly, lifetime of the charge separated state, Fc+-DPP.−-TPA was found to persist longer with an increase in the number of Fc-DPP entities in 4–6 as compared to Fc-DPP-control and simple DPP derived donor–acceptor conjugates in literature. This unprecedented result has been attributed to subtle changes in ΔGCS and ΔGCR and the associated electron coupling between different entities. © 2020 Wiley-VCH GmbHen_US
dc.language.isoenen_US
dc.publisherWiley-VCH Verlagen_US
dc.sourceChemistry - A European Journalen_US
dc.subjectChemical reactionsen_US
dc.subjectEnergy harvestingen_US
dc.subjectFree energyen_US
dc.subjectGibbs free energyen_US
dc.subjectGround stateen_US
dc.subjectIron compoundsen_US
dc.subjectOrganometallicsen_US
dc.subjectRed Shiften_US
dc.subjectSeparationen_US
dc.subjectSpectroelectrochemistryen_US
dc.subjectSpectroscopic analysisen_US
dc.subjectStarsen_US
dc.subjectCharge-separated stateen_US
dc.subjectElectrochemical investigationsen_US
dc.subjectFemtosecond transient absorptionen_US
dc.subjectGibbs free energy calculationsen_US
dc.subjectGround-state interactionsen_US
dc.subjectLight energy harvestingen_US
dc.subjectSonogashira cross-coupling reactionen_US
dc.subjectSpectroelectrochemical studyen_US
dc.subjectExcited statesen_US
dc.titleFormation of Highly Efficient, Long-Lived Charge Separated States in Star-Shaped Ferrocene-Diketopyrrolopyrrole-Triphenylamine Donor–Acceptor–Donor Conjugatesen_US
dc.typeJournal Articleen_US
dc.rights.licenseAll Open Access, Bronze-
Appears in Collections:Department of Chemistry

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