Dibenzonaphthyridinones: Heterocycle-to-Heterocycle Synthetic Strategies and Photophysical Studies

Simple item page
dc.contributor.authorPalazzo, Teresa Ann
dc.contributor.authorPatra, Digambara
dc.contributor.authorYang, Joung S.
dc.contributor.authorEl Khoury, Elsy D.
dc.contributor.authorAppleton, Mackenzie G.
dc.contributor.authorHaddadin, Makhluf J.
dc.contributor.authorTantillo, Dean Joseph
dc.contributor.authorKurth, Mark J.
dc.contributor.departmentDepartment of Chemistry
dc.contributor.facultyFaculty of Arts and Sciences (FAS)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:21:46Z
dc.date.available2025-01-24T11:21:46Z
dc.date.issued2015
dc.description.abstractA heterocycle-to-heterocycle strategy is presented for the preparation of highly fluorescent and solvatochromic dibenzonaphthyridinones (DBNs) via methodology that leads to the formation of a tertiary, spiro-fused carbon center. A linear correlation between the results of photophysical experiments and time dependent density functional theory calculations was observed for the λmax of excitation for DBNs with varying electronic character. © 2015 American Chemical Society.
dc.identifier.doihttps://doi.org/10.1021/acs.orglett.5b02680
dc.identifier.eid2-s2.0-84948843953
dc.identifier.pmid26574652
dc.identifier.urihttp://hdl.handle.net/10938/25309
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.relation.ispartofOrganic Letters
dc.sourceScopus
dc.subjectBenzene derivatives
dc.subjectCombinatorial chemistry techniques
dc.subjectFluorescence
dc.subjectIsoxazoles
dc.subjectModels, chemical
dc.subjectMolecular structure
dc.subjectNaphthyridines
dc.subjectBenzene derivative
dc.subjectIsoxazole derivative
dc.subjectNaphthyridine derivative
dc.subjectChemical model
dc.subjectChemical structure
dc.subjectChemistry
dc.subjectCombinatorial chemistry
dc.subjectSynthesis
dc.titleDibenzonaphthyridinones: Heterocycle-to-Heterocycle Synthetic Strategies and Photophysical Studies
dc.typeArticle

Files

Original bundle

Now showing 1 - 1 of 1
Thumbnail Image
Name:
2015-9844.pdf
Size:
1013.68 KB
Format:
Adobe Portable Document Format
Download

Collections

Department of Chemistry