Synthesis, photophysical and photochemical studies on long chain zinc phthalocyanine derivatives

dc.contributor.authorOgunsipe, Abimbola
dc.contributor.authorDurmuş, Mahmut
dc.contributor.authorAtilla, Devrim
dc.contributor.authorGürek, Ayşe Gül
dc.contributor.authorAhsen, Vefa
dc.contributor.authorNyokong, Tebello
dc.date.accessioned2025-10-29T11:22:41Z
dc.date.issued2008
dc.departmentFakülteler, Temel Bilimler Fakültesi, Kimya Bölümü
dc.description.abstractThe synthesis and characterization of 2,9,16,23-chloro-3,10,17,24-triethyleneoxysulphanylphthalocyaninato zinc(H) (CTESZnPc) is described. The photophysics and photochemistry of CTESZnPc and those of tetrakis(triethyleneoxysulphanyl)zinc phthalocyanine (TTESZnPc) and octakis(triethyleneoxysulphanyl)zinc phthalocyanine (OTESZnPc), are presented and compared with those of unsubstituted zinc phthalocyanine (ZnPc). The presence of triethyleneoxysulphanyl substituents oil the ZnPc ring gave rise to higher values of singlet oxygen (phi(Delta)) and photodegradation (phi(Pd)) quantum yields in DMF However, TTESZnPc, OTESZnPc and CTESZnPc are less fluorescent than ZnPc, judging from their fluorescence quantum yield (phi(F)) values. Fluorescence was lower in toluene than in DMF due to aggregation in the former solvent. Triplet quantum yield (phi(T)) values were found to increase with the presence of substituents oil the ZnPc ring. while triplet lifetimes (tau(T)) were found to vary linearly with the logarithms of solvent viscosities. The fluorescences of the substituted ZnPc complexes were effectively quenched by benzoquinone (BQ). and the quenching data analyzed by the Stern-Volmer equation. The Stern-Volmer constants and the diffusion-controlled bimolecular rate constants were calculated. (C) 2008 Elsevier B.V. All rights reserved,
dc.description.sponsorshipNational Research Foundation of South Africa [NRF GUN 2053657]
dc.description.sponsorshipTUBITAK [104T217]
dc.description.sponsorshipThis work was supported by the National Research Foundation of South Africa (NRF GUN # 2053657) and TUBITAK (Kariyer-104T217) project as well as Rhodes University. AO thanks ANSTI/UNESCO for Staff exchange visit fellowship.
dc.identifier.doi10.1016/j.synthmet.2008.06.007
dc.identifier.endpage847
dc.identifier.issn0379-6779
dc.identifier.issue21-24
dc.identifier.orcid0000-0002-4590-9926
dc.identifier.scopus2-s2.0-57649229435
dc.identifier.scopusqualityQ1
dc.identifier.startpage839
dc.identifier.urihttps://doi.org/10.1016/j.synthmet.2008.06.007
dc.identifier.urihttps://hdl.handle.net/20.500.14854/9054
dc.identifier.volume158
dc.identifier.wosWOS:000262573900010
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherElsevier Science Sa
dc.relation.ispartofSynthetic Metals
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20251020
dc.subjectPhthalocyanine
dc.subjectQuantum yields
dc.subjectSinglet oxygen
dc.subjectPhotodynamic therapy
dc.subjectBenzoquinone
dc.subjectQuenching
dc.titleSynthesis, photophysical and photochemical studies on long chain zinc phthalocyanine derivatives
dc.typeArticle

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