Luminescent 1H-1,3-benzazaphospholes

dc.contributor.authorEvariste, Sloane
dc.contributor.authorHarrison, Alexandra M.
dc.contributor.authorSarkar, Sunandan
dc.contributor.authorRheingold, Arnold L.
dc.contributor.authorDunietz, Barry D.
dc.contributor.authorHeinicke, Joachim W.
dc.contributor.authorDelgado Rosario, Emalyn
dc.contributor.authorYoon, Sungwoon
dc.contributor.authorTeets, Thomas S.
dc.contributor.authorProtasiewicz, John D.
dc.date.accessioned2026-08-25T11:13:29Z
dc.date.available2026-08-25T11:13:29Z
dc.date.issued2022-12-22
dc.description.abstract2-R-1H-1,3-Benzazaphospholes (R-BAPs) are an interesting class of σ2P heterocycles containing P = C bonds. While closely related 2-R-1,3-benzoxaphospholes (R-BOPs) have been shown to be highly photoluminescent materials depending on specific R substituents, photoluminescence of R-BAPs has been previously limited to an example having a fused carbazole ring system. Here we detail the synthesis and structural characterization of a new R-BAP (3c, R = 2,2′-dithiophene), and compare its photoluminescence against two previously reported R-BAPs (3a, R, R′ = Me and 3b, R = 2-thiophene). The significant fluorescence displayed by the thiophene derivatives 3b (φ = 0.53) and 3c (φ = 0.12) stands in contrast to the weakly emissive methyl substituted analogue 3a (φ = 0.08). Comparative computational investigations of 3a-c offer insights into the interplay between structure-function relationships affecting excited state relaxation processes. © 2023 The Royal Society of Chemistry.
dc.identifier.issn20462069
dc.identifier.urihttps://doi.org/10.1039/d2ra07226b
dc.identifier.urihttp://nitt.ndl.gov.in/handle/123456789/246
dc.language.isoen
dc.publisherRoyal Society of Chemistry
dc.titleLuminescent 1H-1,3-benzazaphospholes
dc.typeArticle
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