Structure-Property Evaluation of Knoevenagel-Derived π-Conjugated Organic Systems

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dc.contributor.authorRavikumar, M.V.
dc.contributor.authorRaj, A.K.
dc.contributor.authorRajeswara Rao, M.
dc.contributor.authorLakshmi, V.
dc.date.accessioned2026-02-08T18:38:24Z
dc.date.issued2025
dc.description.abstractπ-Conjugated organic compounds display unique optical and electrical properties, rendering them appropriate for semiconducting applications. Knoevenagel condensation is one of the important reactions that facilitate the formation of olefin linkages (−C=C−) and thus has been widely employed to synthesize new π-conjugated molecules. This review summarizes the synthesis of π-conjugated compounds constructed using four novel π-conjugated moieties: diketonate/azopyrrole-BF<inf>2</inf> complexes (BF), p-azaquinodimethane (AQM), diketopyrrolopyrrole (DPP), and barbituric acid (BA), alongside their optoelectronic features and applications in sensing, bioimaging, and photovoltaic technologies. © 2025 Wiley-VCH GmbH.
dc.identifier.citationEuropean Journal of Organic Chemistry, 2025, Vol.28, 13, p. -
dc.identifier.issn1434193X
dc.identifier.urihttps://doi.org/10.1002/ejoc.202401367
dc.identifier.urihttps://idr.nitk.ac.in/handle/123456789/34131
dc.publisherJohn Wiley and Sons Inc
dc.subjectBarbituric acid
dc.subjectBF2 complexes
dc.subjectDiketopyrrolopyrrole
dc.subjectFluorescence
dc.subjectKnoevenagel condensation
dc.subjectp-Azaquinodimethane
dc.subjectπ-Conjugation
dc.titleStructure-Property Evaluation of Knoevenagel-Derived π-Conjugated Organic Systems

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