An attractive family of cyclometalated Ir(III) dyes functionalized with tryptophan for potential neuroimaging applications
dc.contributor.author | De Soricellis, G. | |
dc.contributor.author | Fagnani, F. | |
dc.contributor.author | Colombo, A. | |
dc.contributor.author | Dragonetti, C. | |
dc.contributor.author | Roberto, D. | |
dc.contributor.author | Marinotto, D. | |
dc.contributor.author | Hartnell, D.H. | |
dc.contributor.author | Hackett, Mark | |
dc.contributor.author | Massi, Max | |
dc.contributor.author | Carboni, B. | |
dc.contributor.author | Guerchais, V. | |
dc.date.accessioned | 2024-11-28T02:57:06Z | |
dc.date.available | 2024-11-28T02:57:06Z | |
dc.date.issued | 2023 | |
dc.identifier.citation | De 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.uri | http://hdl.handle.net/20.500.11937/96433 | |
dc.identifier.doi | 10.1016/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.language | English | |
dc.publisher | ELSEVIER SCI LTD | |
dc.relation.sponsoredby | http://purl.org/au-research/grants/arc/DP220103091 | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.subject | Science & Technology | |
dc.subject | Physical Sciences | |
dc.subject | Technology | |
dc.subject | Chemistry, Applied | |
dc.subject | Engineering, Chemical | |
dc.subject | Materials Science, Textiles | |
dc.subject | Chemistry | |
dc.subject | Engineering | |
dc.subject | Materials Science | |
dc.subject | Iridium dyes | |
dc.subject | Cyclometalated iridium(III) phenanthroline | |
dc.subject | complexes | |
dc.subject | Phosphorescence | |
dc.subject | Bio-imaging | |
dc.subject | Optical markers | |
dc.subject | Brain tissue staining | |
dc.subject | NONLINEAR-OPTICAL PROPERTIES | |
dc.subject | EXCITED-STATE PROPERTIES | |
dc.subject | IRIDIUM(III) COMPLEXES | |
dc.subject | 2-PHOTON ABSORPTION | |
dc.subject | SUBSTITUTED 1,10-PHENANTHROLINES | |
dc.subject | ELECTROLUMINESCENT DEVICES | |
dc.subject | ENDOPLASMIC-RETICULUM | |
dc.subject | PHOTOREDOX CATALYSIS | |
dc.subject | III COMPLEXES | |
dc.subject | LIGHT | |
dc.title | An attractive family of cyclometalated Ir(III) dyes functionalized with tryptophan for potential neuroimaging applications | |
dc.type | Journal Article | |
dcterms.source.volume | 210 | |
dcterms.source.issn | 0143-7208 | |
dcterms.source.title | Dyes and Pigments | |
dc.date.updated | 2024-11-28T02:57:06Z | |
curtin.department | School of Molecular and Life Sciences (MLS) | |
curtin.accessStatus | Open access | |
curtin.faculty | Faculty of Science and Engineering | |
curtin.contributor.orcid | Massi, Max [0000-0001-6949-4019] | |
curtin.contributor.orcid | Hackett, Mark [0000-0002-3296-7270] | |
curtin.identifier.article-number | ARTN 111012 | |
dcterms.source.eissn | 1873-3743 | |
curtin.contributor.scopusauthorid | Massi, Max [7102368846] | |
curtin.contributor.scopusauthorid | Hackett, Mark [35240056500] [57999521300] | |
curtin.repositoryagreement | V3 |