Publication:
2,6-distyrene substituted meso phenyl/carbazole BODIPY derivatives: Synthesis, Characterization and Optical Features

dc.contributor.authorÖZDEMİR, MÜCAHİT
dc.contributor.authorYALÇIN, BAHATTİN
dc.contributor.authorsKÖKSOY B., ÖZDEMİR M., ALTINIŞIK S., KOYUNCU S., YALÇIN B.
dc.date.accessioned2023-11-06T12:19:54Z
dc.date.available2023-11-06T12:19:54Z
dc.date.issued2023-08-23
dc.description.abstract4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) compounds have emerged as an important central structure that has attracted attention by scientists in recent years with their strong absorption bands, high fluorescence quantum yields and interesting optical properties.. Its multifunctional structure facilitates the design and synthesis of molecules for the desired application. In particular, it has been reported in the literature that BODIPY derivatives substituted from the 2nd and 6th position are used in some applications such as optoelectronic materials [1], electrochemical sensors [2], energy casettes [3] and photopatterning studies [4]. In this study, BODIPY compounds containing styrene groups in the 2nd and 6th positions were synthesized and their structures were characterized by common characterization methods. In addition, the optical properties and crystal structures of the original molecules were studied.
dc.identifier.citationKÖKSOY B., ÖZDEMİR M., ALTINIŞIK S., KOYUNCU S., YALÇIN B., \"2,6-distyrene substituted meso phenyl/carbazole BODIPY derivatives: Synthesis, Characterization and Optical Features\", 19th Asian Chemical Congress, İstanbul, Türkiye, 9 - 14 Temmuz 2023
dc.identifier.urihttps://drive.google.com/file/d/1cMQSgXkg_lRMKG2I7qHQuU_51wuIGhTc/view
dc.identifier.urihttps://hdl.handle.net/11424/294627
dc.language.isoeng
dc.relation.ispartof19th Asian Chemical Congress
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.title2,6-distyrene substituted meso phenyl/carbazole BODIPY derivatives: Synthesis, Characterization and Optical Features
dc.typeconferenceObject
dspace.entity.typePublication
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relation.isAuthorOfPublication8ce578f0-69d2-471b-ae61-0d2526613f8f
relation.isAuthorOfPublication6405e2ff-5dd8-487d-a639-ac5fcc0832bc
relation.isAuthorOfPublication.latestForDiscovery8ce578f0-69d2-471b-ae61-0d2526613f8f

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