Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/13231
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dc.contributor.authorNazlı, İbrahim Hanifen_US
dc.contributor.authorYakalı, Gülen_US
dc.contributor.authorTopkaya, Deryaen_US
dc.contributor.authorİzmirli, Merveen_US
dc.contributor.authorUzun, Sema Demircien_US
dc.contributor.authorAlp, Serapen_US
dc.date.accessioned2023-03-13T13:05:08Z-
dc.date.available2023-03-13T13:05:08Z-
dc.date.issued2023-
dc.identifier.issn1053-0509-
dc.identifier.urihttps://doi.org/10.1007/s10895-023-03158-7-
dc.identifier.urihttps://hdl.handle.net/11147/13231-
dc.description.abstractMost of the fluorescent molecules among organic π-conjugated materials show blue or green emission in the solid phase but few of them emit red-shifted visible and near-infrared light in the material science. To create molecules emitting for this feature, two π-conjugated oxazol-5-one derivatives containing donor (OCH3) and acceptor groups (NO2) were synthesized. Their optical and charge-transport properties were investigated through experimental and theoretical methods including the single crystal X-ray crystallography, Hirshfeld Surface Analysis, photophysical studies and Density Functional Theory (DFT), respectively. In addition, FT-IR, 1H-NMR, 13C-NMR spectroscopy, cyclic voltammetry (CV) measurements were performed. According to our results, both molecules may provide the significant pathway of development of long wavelength visible and red emissive features in solid phase with the aggregation induced enhanced emission (AIEE) properties particularly in the fields of OLEDs, optical communication, defence and bioimaging.en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.ispartofJournal of Fluorescenceen_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectAggregation induced enhanced emission (AIEE)en_US
dc.subjectNoncovalent interactionsen_US
dc.subjectStacking interactionsen_US
dc.titleTuning the solid phase fluorescence emission from long wavelength visible to near-ınfrared in oxazol-5-one derivatives: structure–property relationship, theoretical and experimental studiesen_US
dc.typeArticleen_US
dc.authorid0000-0002-7705-2349en_US
dc.institutionauthorNazlı, İbrahim Hanifen_US
dc.departmentİzmir Institute of Technology. Chemistryen_US
dc.identifier.wosWOS:000932804300001en_US
dc.identifier.scopus2-s2.0-85147740375en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1007/s10895-023-03158-7-
dc.identifier.pmid36763296-
dc.contributor.affiliation01. Izmir Institute of Technologyen_US
dc.contributor.affiliationİzmir Katip Çelebi Üniversitesien_US
dc.contributor.affiliationDokuz Eylül Üniversitesien_US
dc.contributor.affiliationDokuz Eylül Üniversitesien_US
dc.contributor.affiliationİzmir Katip Çelebi Üniversitesien_US
dc.contributor.affiliationDokuz Eylül Üniversitesien_US
dc.relation.issn1053-0509en_US
dc.identifier.wosqualityQ3-
dc.identifier.scopusqualityQ3-
item.fulltextWith Fulltext-
item.grantfulltextembargo_20250701-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeArticle-
crisitem.author.dept01. Izmir Institute of Technology-
Appears in Collections:Chemistry / Kimya
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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