Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9443
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dc.contributor.authorMisra, Rajneeshen_US
dc.contributor.authorMobin, Shaikh M.en_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:33:07Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:33:07Z-
dc.date.issued2013-
dc.identifier.citationJadhav, T., Maragani, R., Misra, R., Sreeramulu, V., Rao, D. N., & Mobin, S. M. (2013). Design and synthesis of donor-acceptor pyrazabole derivatives for multiphoton absorption. Dalton Transactions, 42(13), 4340-4342. doi:10.1039/c3dt33065fen_US
dc.identifier.issn1477-9226-
dc.identifier.otherEID(2-s2.0-84874925249)-
dc.identifier.urihttps://doi.org/10.1039/c3dt33065f-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9443-
dc.description.abstractA series of ferrocenyl substituted pyrazaboles were prepared, which have an electron-withdrawing pyrazabole moiety as the central core, with a D-π-A-π-D structural motif (D = donor, A = acceptor) and containing a variety of π bridges. A crystallographic study reveals that the pyrazabole central core was observed in planar geometry. Strong two-photon absorption in the visible region and three-photon absorption in the near IR region were observed in the ferrocenyl substituted pyrazaboles. It was observed that the 2PA absorption cross-section increases with the conjugation length. © The Royal Society of Chemistry 2013.en_US
dc.language.isoenen_US
dc.sourceDalton Transactionsen_US
dc.subjectAbsorption cross-sectionen_US
dc.subjectConjugation lengthen_US
dc.subjectCrystallographic studiesen_US
dc.subjectElectronwithdrawingen_US
dc.subjectMulti-photon absorptionen_US
dc.subjectStructural motifsen_US
dc.subjectThree photon absorptionen_US
dc.subjectTwo-photon absorptionsen_US
dc.subjectSingle crystalsen_US
dc.subjectTwo photon processesen_US
dc.subjectLight absorptionen_US
dc.titleDesign and synthesis of donor-acceptor pyrazabole derivatives for multiphoton absorptionen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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