Publication:
Novel tetrakis 4-(hydroxymethyl)-2,6-dimethoxyphenoxyl substituted metallophthalocyanines: Synthesis, electrochemical redox, electrocatalytic oxygen reducing, and volatile organic compounds sensing and adsorption properties

dc.contributor.authorÖZKAYA, ALİ RIZA
dc.contributor.authorORMAN, EFE BATURHAN
dc.contributor.authorÖZER, METİN
dc.contributor.authorsGunay, Ipek; Orman, Efe Baturhan; Altindal, Ahmet; Salih, Bekir; Ozer, Metin; Ozkaya, Ali Riza
dc.date.accessioned2022-03-12T22:26:25Z
dc.date.accessioned2026-01-11T10:25:43Z
dc.date.available2022-03-12T22:26:25Z
dc.date.issued2018
dc.description.abstractNovel tetrakis [(4-(hydroxymethyl)-2,6-dimethoxyphenoxyl)] substituted zinc(II), cobalt(II) and iron(II) phthalocyanines were synthesized by the reaction of (4-(hydroxymethyl)-2,6-dimethoxyphenoxy)phthalonitrile with suitable metal salts in 2-N, N-dimethylaminoethanol. The phthalonitrile ligand was prepared from 4-hydroxy-3,5-dimethoxy benzyl alcohol and 4-nitrophthalonitrile using potassium carbonate as catalyst in N,N-dimethylformamide at 50 degrees C. The structural characterization of the compounds was carried out by elemental analysis, FTIR, UV-vis and MALDI-TOF Mass spectroscopic methods. Electron transfer properties and electrocatalytic oxygen reducing performances of the compounds were also investigated by electrochemical, in situ spectroelectrochemical and in situ electrocolorimetric measurements. Electrochemical, in situ spectroelectrochemical, and in situ electrocolorimetric measurements showed that rich redox behavior of the complexes leads to their high electrocatalytic activity for oxygen reduction and net electrocolorimetric changes suitable for electrochromic applications. Phthalocyanine central metal ion effect on the sensing properties and the adsorption kinetics of four main groups of volatile organic compounds (alkanes, alcohols, chlorinated hydrocarbons and amines) onto these novel compounds were also examined by three different models. While the sensitivity of the sensors was strongly dependent on the nature of the metal ion, no considerable effect was observed on the adsorption kinetics. The evaluation of the kinetics of adsorption processes with respect to three different models showed that pseudo second order rate equation best describes the adsorption of alcohols and chlorinated hydrocarbons while the adsorption of alkanes and amines on these compounds can be represented by Elovich equation.
dc.identifier.doi10.1016/j.dyepig.2018.02.037
dc.identifier.eissn1873-3743
dc.identifier.issn0143-7208
dc.identifier.urihttps://hdl.handle.net/11424/235062
dc.identifier.wosWOS:000432501000023
dc.language.isoeng
dc.publisherELSEVIER SCI LTD
dc.relation.ispartofDYES AND PIGMENTS
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectPhthalocyanine
dc.subjectElectrochemistry
dc.subjectIn situ spectroelectrochemistry
dc.subjectOxygen electrocatalysis
dc.subjectVOC sensing
dc.subjectVOC adsorption
dc.subjectHETERO-DINUCLEAR PHTHALOCYANINES
dc.subjectIN-SITU SPECTROELECTROCHEMISTRY
dc.subjectDECKER LU(III) PHTHALOCYANINES
dc.subjectBALL-TYPE PHTHALOCYANINES
dc.subjectMETAL-FREE
dc.subjectTHIN-FILMS
dc.subjectELECTRICAL-PROPERTIES
dc.subjectCOBALT PHTHALOCYANINES
dc.subjectREDUCTION REACTION
dc.subjectBEARING COUMARIN
dc.titleNovel tetrakis 4-(hydroxymethyl)-2,6-dimethoxyphenoxyl substituted metallophthalocyanines: Synthesis, electrochemical redox, electrocatalytic oxygen reducing, and volatile organic compounds sensing and adsorption properties
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage187
oaire.citation.startPage172
oaire.citation.titleDYES AND PIGMENTS
oaire.citation.volume154

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