Photophysical and photodynamic properties of Pyronin Y in micellar media at different temperatures

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In this study, photophysics and photodynamical properties of Pyronin Y (PyY) in different liquid media were investigated. Interactions of PyY, which is a positively charged pigment compound pertaining to the xanthene derivatives with surfactants possessing distinct charges, were determined by using the molecular absorption and fluorescence spectroscopy techniques. It was observed that band intensities of absorption and fluorescence spectra belonging to PyY increase in proportion to the water when compared to three micelle systems, cetyltrimethylammonium bromide (CTAB), sodium dodecyl sulfate (SDS) and Triton X-100 (TX-100). This suggests that interactions in micelle systems are different from those in deionized water, and solvation and surface interactions modify. It is determined that the strongest interaction occurs between PyY dye and SDS, anionic surfactant, and this interaction arises from the electrostatic forces. Calculated photophysical parameters indicated that the microenvironment of PyY in SDS micelle is different to that of other systems. In temperature studies, it was reported that increasing the temperature of the samples increased non-radiative transitions. Steady-state fluorescence anisotropy values were calculated by using fluorescence intensities of PyY compound in pre-micellar, micellar and post-micellar systems. Once the PyY fluorescence probe is added to the surfactant containing solutions below the critical micelle concentrations, the measured anisotropy values were found to be low because the probe remains in the deionized water phase. When the surfactant concentration of the medium becomes closer to the critical micelle concentrations, the steady-state anisotropy value prominently increases. This is because of the restrictions on the rotational diffusion of the probe in micellar solution. It is observed that positively charged PyY shows a higher affinity to the negatively charged SDS compared with the positively charged CTAB and neutral TX-100 surfactants. This can be explained by Coulombic interactions. © 2019 John Wiley & Sons, Ltd.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/13556Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1002/bio.3624Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorBeşer, Burcu Meryem
dc.contributor.authorArik, Mustafa
dc.contributor.authorOnganer, Yavuz
dc.date.accessioned2026-10-18T20:28:23.430808413Z
dc.date.available2026-10-18T20:28:23.430808413Z
dc.date.issued2019
dc.description.abstractIn this study, photophysics and photodynamical properties of Pyronin Y (PyY) in different liquid media were investigated. Interactions of PyY, which is a positively charged pigment compound pertaining to the xanthene derivatives with surfactants possessing distinct charges, were determined by using the molecular absorption and fluorescence spectroscopy techniques. It was observed that band intensities of absorption and fluorescence spectra belonging to PyY increase in proportion to the water when compared to three micelle systems, cetyltrimethylammonium bromide (CTAB), sodium dodecyl sulfate (SDS) and Triton X-100 (TX-100). This suggests that interactions in micelle systems are different from those in deionized water, and solvation and surface interactions modify. It is determined that the strongest interaction occurs between PyY dye and SDS, anionic surfactant, and this interaction arises from the electrostatic forces. Calculated photophysical parameters indicated that the microenvironment of PyY in SDS micelle is different to that of other systems. In temperature studies, it was reported that increasing the temperature of the samples increased non-radiative transitions. Steady-state fluorescence anisotropy values were calculated by using fluorescence intensities of PyY compound in pre-micellar, micellar and post-micellar systems. Once the PyY fluorescence probe is added to the surfactant containing solutions below the critical micelle concentrations, the measured anisotropy values were found to be low because the probe remains in the deionized water phase. When the surfactant concentration of the medium becomes closer to the critical micelle concentrations, the steady-state anisotropy value prominently increases. This is because of the restrictions on the rotational diffusion of the probe in micellar solution. It is observed that positively charged PyY shows a higher affinity to the negatively charged SDS compared with the positively charged CTAB and neutral TX-100 surfactants. This can be explained by Coulombic interactions. © 2019 John Wiley & Sons, Ltd.
dc.identifier.doi10.1002/bio.3624
dc.identifier.eissn1522-7243
dc.identifier.endpage425
dc.identifier.issn1522-7235
dc.identifier.issue4
dc.identifier.pmid30868727
dc.identifier.scopus2-s2.0-85062967920
dc.identifier.startpage415
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/13556
dc.identifier.volume34
dc.identifier.wosWOS:000467485600004
dc.language.isoen
dc.publisherJohn Wiley and Sons Ltd
dc.relation.ispartofLuminescence
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectdye–surfactant interactions
dc.subjectphotodynamics
dc.subjectphotophysics
dc.subjectPyronin Y
dc.subjectAnisotropy
dc.subjectFluorescence
dc.subjectFluorescent Dyes
dc.subjectMicelles
dc.subjectMolecular Structure
dc.subjectPhotochemical Processes
dc.subjectPyronine
dc.subjectSurface-Active Agents
dc.subjectTemperature
dc.subjectCritical micelle concentration
dc.subjectDeionized water
dc.subjectFluorescence spectroscopy
dc.subjectProbes
dc.subjectSulfur compounds
dc.subjectWater absorption
dc.subjectfluorescent dye
dc.subjectsurfactant
dc.subjectCetyltrimethylammonium bromide
dc.subjectDye-surfactant interaction
dc.subjectMiceller systems
dc.subjectPhotodynamic
dc.subjectPositively charged
dc.subjectProperty
dc.subjectSodium dodecyl sulphate
dc.subjectTriton X-100
dc.subjectchemical structure
dc.titlePhotophysical and photodynamic properties of Pyronin Y in micellar media at different temperatures
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus10
rdl.citation.wos9
rdl.departmentDepartment of Chemistry, Erzincan Binali Yıldırım University, Erzincan, Turkey.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)