The Role of Electron-Donating Subunits in Cross-Linked BODIPY Polymer Films
| dc.contributor.author | Özdemir, Mücahit | |
| dc.contributor.author | Köksoy, Baybars | |
| dc.contributor.author | Yalcin, B. | |
| dc.contributor.author | Koyuncu, Sermet | |
| dc.date.accessioned | 2026-02-08T15:11:03Z | |
| dc.date.available | 2026-02-08T15:11:03Z | |
| dc.date.issued | 2024 | |
| dc.department | Bursa Teknik Üniversitesi | |
| 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. © 2023 The Authors. Macromolecular Rapid Communications published by Wiley-VCH GmbH. | |
| dc.description.sponsorship | Marmara Üniversitesi, (FDK-2022-10521) | |
| dc.identifier.doi | 10.1002/marc.202300552 | |
| dc.identifier.issn | 1022-1336 | |
| dc.identifier.issue | 4 | |
| dc.identifier.pmid | 37962095 | |
| dc.identifier.scopus | 2-s2.0-85178096135 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.uri | https://doi.org/10.1002/marc.202300552 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12885/5201 | |
| dc.identifier.volume | 45 | |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | PubMed | |
| dc.language.iso | en | |
| dc.publisher | John Wiley and Sons Inc | |
| dc.relation.ispartof | Macromolecular Rapid Communications | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.snmz | Scopus_KA_20260207 | |
| 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 |












