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dc.contributor.authorDe Soricellis, G.
dc.contributor.authorFagnani, F.
dc.contributor.authorColombo, A.
dc.contributor.authorDragonetti, C.
dc.contributor.authorRoberto, D.
dc.contributor.authorMarinotto, D.
dc.contributor.authorHartnell, D.H.
dc.contributor.authorHackett, Mark
dc.contributor.authorMassi, Max
dc.contributor.authorCarboni, B.
dc.contributor.authorGuerchais, V.
dc.date.accessioned2024-11-28T02:57:06Z
dc.date.available2024-11-28T02:57:06Z
dc.date.issued2023
dc.identifier.citationDe Soricellis, G. and Fagnani, F. and Colombo, A. and Dragonetti, C. and Roberto, D. and Marinotto, D. and Hartnell, D.H. et al. 2023. An attractive family of cyclometalated Ir(III) dyes functionalized with tryptophan for potential neuroimaging applications. Dyes and Pigments. 210: ARTN 111012.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/96433
dc.identifier.doi10.1016/j.dyepig.2022.111012
dc.description.abstract

Three novel luminescent iridium(III) dyes functionalized with a tryptophan amino acid and bearing two cyclometalated 2-phenylpyridines, 2-(2,4-difluorophenyl)pyridines or 2-phenylquinolines have been prepared and well characterized. They emit at 522–561 nm with a luminescence quantum yield in the range 0.33–0.98. All the dyes are able to stain neuronal cells in rat cerebellum tissue, as evidenced by fluorescence microscopy, showing affinity for granule neurons. The complexes bearing cyclometalated 2-(2,4-difluorophenyl)pyridines or 2-phenylquinolines also have a good affinity for brain white matter. The dye with two cyclometalated 2-phenylquinolines is characterized by the best luminescence quantum yield (0.98). Besides, giving the greatest image contrast, the dye with two cyclometalated 2-phenylquinolines shows the strongest affinity for a distinct subtype of neurons found in cerebellum tissue, the purkinje neurons (as evidenced with fluorescence microscopy).

dc.languageEnglish
dc.publisherELSEVIER SCI LTD
dc.relation.sponsoredbyhttp://purl.org/au-research/grants/arc/DP220103091
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectScience & Technology
dc.subjectPhysical Sciences
dc.subjectTechnology
dc.subjectChemistry, Applied
dc.subjectEngineering, Chemical
dc.subjectMaterials Science, Textiles
dc.subjectChemistry
dc.subjectEngineering
dc.subjectMaterials Science
dc.subjectIridium dyes
dc.subjectCyclometalated iridium(III) phenanthroline
dc.subjectcomplexes
dc.subjectPhosphorescence
dc.subjectBio-imaging
dc.subjectOptical markers
dc.subjectBrain tissue staining
dc.subjectNONLINEAR-OPTICAL PROPERTIES
dc.subjectEXCITED-STATE PROPERTIES
dc.subjectIRIDIUM(III) COMPLEXES
dc.subject2-PHOTON ABSORPTION
dc.subjectSUBSTITUTED 1,10-PHENANTHROLINES
dc.subjectELECTROLUMINESCENT DEVICES
dc.subjectENDOPLASMIC-RETICULUM
dc.subjectPHOTOREDOX CATALYSIS
dc.subjectIII COMPLEXES
dc.subjectLIGHT
dc.titleAn attractive family of cyclometalated Ir(III) dyes functionalized with tryptophan for potential neuroimaging applications
dc.typeJournal Article
dcterms.source.volume210
dcterms.source.issn0143-7208
dcterms.source.titleDyes and Pigments
dc.date.updated2024-11-28T02:57:06Z
curtin.departmentSchool of Molecular and Life Sciences (MLS)
curtin.accessStatusOpen access
curtin.facultyFaculty of Science and Engineering
curtin.contributor.orcidMassi, Max [0000-0001-6949-4019]
curtin.contributor.orcidHackett, Mark [0000-0002-3296-7270]
curtin.identifier.article-numberARTN 111012
dcterms.source.eissn1873-3743
curtin.contributor.scopusauthoridMassi, Max [7102368846]
curtin.contributor.scopusauthoridHackett, Mark [35240056500] [57999521300]
curtin.repositoryagreementV3


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