Tunable Green Emitting Novel Phosphazene Compounds via Azide-Alkyne Cycloaddition: Evaluation of Photodiode Performance, Synthesis, and Photophysical Characterization

dc.contributor.authorSeker, Ferhan Sultan
dc.contributor.authorCetiner, Rumeysa
dc.contributor.authorKane, Labouda
dc.contributor.authorAkman, Feride
dc.contributor.authorBiryan, Fatih
dc.contributor.authorCaliskan, Eray
dc.contributor.authorKoran, Kenan
dc.date.accessioned2026-08-12T17:42:55Z
dc.date.issued2026
dc.departmentFırat Üniversitesi
dc.description.abstractThis study aims to develop new photodiode materials containing functional chalcone derivatives by combining the electronic properties of the cyclotriphosphazene ring with click chemistry. Azide-terminated chalcones were subjected to a click reaction with an alkyne-functionalized dispirocylotriphosphazene (Bif-PA) to afford the Bif-PA-Click-Chal 1-4 compounds, whose structural characterizations were confirmed by FT-IR, NMR, and MALDI-TOF MS analyses. Photophysical properties were investigated using UV-vis and fluorescence spectroscopy, and the Bif-PA-Click-Chal 1 compound exhibited a quantum yield of 0.32 and high emission intensity. For the Bif-PA-Click-Chal 1 molecule, absorption parameters were calculated using CPCM/6-31G(d,p) and TD-DFT/CAM-B3LYP methods (in THF), revealing a theoretical bandgap of 3.53 eV, whereas experimental UV-vis measurements indicated a bandgap of 2.69 eV. Electrical measurements were performed to investigate the I-V characteristics of the new types of diodes fabricated using the Bif-PA-Click-Chal 1-4 compounds. Among these, Bif-PA-Click-Chal 1 and 2 demonstrated diode performance. Comparison of their diode properties showed that both compounds behaved as semiconductors exhibiting diode characteristics. Bif-PA-Click-Chal 2 stood out with a high rectification ratio (RR = 523.64), low saturation current (I 0 = 1.27 x 10-8 A), a better ideality factor (n = 2.51), and high barrier height (phi b = 0.76 eV). However, measurements performed under various light intensities indicated that it did not exhibit photodiode behavior. In contrast, Bif-PA-Click-Chal 1, despite displaying a lower rectification ratio (RR = 80.45), higher saturation current (I 0 = 2.38 x 10-8 A), and an ideality factor of n = 2.73, demonstrated photodiode behavior under different light intensities. These findings confirm that both compounds exhibit diode characteristics; however, the photodiode behavior of Bif-PA-Click-Chal 1 and its superior I-V characterization reveal that it possesses enhanced electronic and photoconductive properties compared to its counterparts.
dc.description.sponsorshipFirat University Scientific Research Projects Management Unit [1919B012216312]
dc.description.sponsorshipThe authors dedicated this publication to the 50th anniversary of F & imath;rat University. This study was supported by F & imath;rat University Scientific Research Projects Coordination Unit (FUBAP) with the project number FF.25.25 and by TUBITAK BIDEB project number 1919B012216312. The authors express their sincere appreciation to TRUBA for providing the Gaussian 16 software and to Bitlis Eren University for their support with Gausview 5.0.
dc.identifier.doi10.1021/acs.inorgchem.5c04900
dc.identifier.endpage1335
dc.identifier.issn0020-1669
dc.identifier.issn1520-510X
dc.identifier.issue2
dc.identifier.orcid0000-0003-2399-4100
dc.identifier.pmid41492973
dc.identifier.scopus2-s2.0-105027628708
dc.identifier.scopusqualityQ1
dc.identifier.startpage1314
dc.identifier.urihttps://doi.org/10.1021/acs.inorgchem.5c04900
dc.identifier.urihttps://hdl.handle.net/11508/59926
dc.identifier.volume65
dc.identifier.wosWOS:001655290700001
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherAmer Chemical Soc
dc.relation.ispartofInorganic Chemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectDielectric-Properties
dc.subjectSeries Resistance
dc.subjectClick Chemistry
dc.subjectBand-Gap
dc.subjectFluorescence
dc.subjectDiodes
dc.subjectCyclophosphazenes
dc.subjectTemperature
dc.subjectFabrication
dc.subjectDependence
dc.titleTunable Green Emitting Novel Phosphazene Compounds via Azide-Alkyne Cycloaddition: Evaluation of Photodiode Performance, Synthesis, and Photophysical Characterization
dc.typeArticle

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