Publication: The role of electron-donating subunits in cross-linked BODIPY polymer films
dc.contributor.author | ÖZDEMİR, MÜCAHİT | |
dc.contributor.author | YALÇIN, BAHATTİN | |
dc.contributor.authors | ÖZDEMİR M., Köksoy B., YALÇIN B., KOYUNCU S. | |
dc.date.accessioned | 2023-12-11T08:41:26Z | |
dc.date.available | 2023-12-11T08:41:26Z | |
dc.date.issued | 2023-01-01 | |
dc.description.abstract | A new method for synthesizing cross-linked 4,4-difluoro-4-bora-3a,4a-diaza-s-indacenes (BODIPYs) using a radical-based thiol-ene click reaction is developed. This method is simple, efficient, and cost-effective, and it produces polymers with unique optical, electrochemical, and surface morphology properties. Significant blue shifts in absorption and photoinduced electron transfer in emissions are observed in the cross-linked BODIPY thin films. Cross-linking also leads to the restriction of conjugation, which results in the breakage of the terminal vinyl group, an increase in the oxidation potential, and a slight upshift in the HOMO position. As a result, the electrochemical band gap is widened from 1.88 to 1.94 eV for polymer bearing N,N-dimethylamino-BODIPY and from 1.97 to 2.02 eV for polymer bearing N,N-diphenylamino-BODIPY moieties. Monomer thin films form planar surfaces due to crystallinity, while amorphous cross-linked BODIPY polymers form more rough surfaces. Additionally, photopatterning on the film surface is successfully performed using different patterned masks. This new method for synthesizing cross-linked BODIPYs has the potential to be used in a variety of applications, including organic electronics, bioimaging, and photocatalysis. | |
dc.identifier.citation | ÖZDEMİR M., Köksoy B., YALÇIN B., KOYUNCU S., "The Role of Electron-Donating Subunits in Cross-Linked BODIPY Polymer Films", Macromolecular Rapid Communications, 2023 | |
dc.identifier.doi | 10.1002/marc.202300552 | |
dc.identifier.issn | 1022-1336 | |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85178096135&origin=inward | |
dc.identifier.uri | https://hdl.handle.net/11424/295527 | |
dc.language.iso | eng | |
dc.relation.ispartof | Macromolecular Rapid Communications | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | Kimya | |
dc.subject | Biyokimya | |
dc.subject | Biyoinorganik Kimya | |
dc.subject | Fizikokimya | |
dc.subject | Polimer Karakterizasyonu | |
dc.subject | Temel Bilimler | |
dc.subject | Mühendislik ve Teknoloji | |
dc.subject | Chemistry | |
dc.subject | Biochemistry | |
dc.subject | Bioinorganic Chemistry | |
dc.subject | Physical Chemistry | |
dc.subject | Characterization of Polymers | |
dc.subject | Natural Sciences | |
dc.subject | Engineering and Technology | |
dc.subject | Mühendislik, Bilişim ve Teknoloji (ENG) | |
dc.subject | Temel Bilimler (SCI) | |
dc.subject | Malzeme Bilimi | |
dc.subject | POLİMER BİLİMİ | |
dc.subject | KİMYA, ORGANİK | |
dc.subject | MALZEME BİLİMİ, ÇOKDİSİPLİNLİ | |
dc.subject | Engineering, Computing & Technology (ENG) | |
dc.subject | Natural Sciences (SCI) | |
dc.subject | MATERIALS SCIENCE | |
dc.subject | CHEMISTRY | |
dc.subject | POLYMER SCIENCE | |
dc.subject | CHEMISTRY, ORGANIC | |
dc.subject | MATERIALS SCIENCE, MULTIDISCIPLINARY | |
dc.subject | Polimerler ve Plastikler | |
dc.subject | Fizik Bilimleri | |
dc.subject | Organik Kimya | |
dc.subject | Malzeme Kimyası | |
dc.subject | Polymers and Plastics | |
dc.subject | Physical Sciences | |
dc.subject | Organic Chemistry | |
dc.subject | Materials Chemistry | |
dc.subject | 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene | |
dc.subject | electron donating groups | |
dc.subject | optical properties | |
dc.subject | photopatterning | |
dc.subject | surface morphology | |
dc.subject | thiol-ene click | |
dc.title | The role of electron-donating subunits in cross-linked BODIPY polymer films | |
dc.type | article | |
dspace.entity.type | Publication | |
local.avesis.id | 1b9ecee0-1500-420f-a09f-b29208a3df65 | |
local.indexed.at | PUBMED | |
local.indexed.at | SCOPUS | |
relation.isAuthorOfPublication | 8ce578f0-69d2-471b-ae61-0d2526613f8f | |
relation.isAuthorOfPublication | 6405e2ff-5dd8-487d-a639-ac5fcc0832bc | |
relation.isAuthorOfPublication.latestForDiscovery | 8ce578f0-69d2-471b-ae61-0d2526613f8f |
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