Do the positions of trimethyl groups on phthalocyanine photosensitizers improve their photochemical and photophysical properties?

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dc.authoridodabas, zafer/0000-0002-0647-0404
dc.authoridPiskin, Mehmet/0000-0002-4572-4905
dc.contributor.authorCetinkaya, Mehmet
dc.contributor.authorPiskin, Mehmet
dc.contributor.authorAltun, Selcuk
dc.contributor.authorOdabas, Zafer
dc.contributor.authorDurmus, Mahmut
dc.date.accessioned2025-01-27T21:00:25Z
dc.date.available2025-01-27T21:00:25Z
dc.date.issued2017
dc.departmentÇanakkale Onsekiz Mart Üniversitesi
dc.description.abstractThe synthesis of novel highly soluble and non-aggregated metal-free and zinc(II) phthalocyanines containing four 2,3,5-trimethylphenoxy groups was achieved by starting phthalonitrile compounds. The phthalocyanines were characterized by elemental analysis, infrared, ultraviolet-visible and matrix assisted laser desorption/ionization time-of-flight mass spectroscopic techniques. Their photochemical and photophysical properties were also investigated in N,N-dimethylformamide. In addition, the influences of position of methyl groups on phenoxy unit and nature of metal in phthalocyanine cavity on photophysical and photochemical properties were investigated by comparing with previous analogues (phthalocyanines with 2,3,6-trimethylphenoxy and 2,4,6-trimethylphenoxy groups). (C) 2016 Elsevier B.V. All rights reserved.
dc.description.sponsorshipMarmara University, The Commission of Scientific Research Projects (BAPKO) [FEN-C-YLP-041213-0459]
dc.description.sponsorshipWe are thankful to Marmara University, The Commission of Scientific Research Projects (BAPKO) (Project No: FEN-C-YLP-041213-0459)
dc.identifier.doi10.1016/j.jphotochem.2016.11.009
dc.identifier.endpage25
dc.identifier.issn1010-6030
dc.identifier.scopus2-s2.0-84996721549
dc.identifier.scopusqualityQ1
dc.identifier.startpage17
dc.identifier.urihttps://doi.org/10.1016/j.jphotochem.2016.11.009
dc.identifier.urihttps://hdl.handle.net/20.500.12428/27017
dc.identifier.volume335
dc.identifier.wosWOS:000393529000003
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherElsevier Science Sa
dc.relation.ispartofJournal of Photochemistry and Photobiology A-Chemistry
dc.relation.publicationcategoryinfo:eu-repo/semantics/openAccess
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20250125
dc.subjectPhthalocyanine
dc.subject2,3,5-Trimethylphenoxy
dc.subjectPhotosensitizer
dc.subjectPhotophysical
dc.subjectPhotochemical
dc.titleDo the positions of trimethyl groups on phthalocyanine photosensitizers improve their photochemical and photophysical properties?
dc.typeArticle

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