Publication:
Voltammetric and spectroelectrochemical characterization of porphyrazines: Electrochemical metal sensor

dc.contributor.authorKOCA, ATIF
dc.contributor.authorsKoca, Atif; Gonca, Erguen; Guel, Ahmet
dc.date.accessioned2022-03-12T17:35:05Z
dc.date.accessioned2026-01-11T15:12:37Z
dc.date.available2022-03-12T17:35:05Z
dc.date.issued2008
dc.description.abstractVoltammetric and spectroelectrochemical characterization of the metallo-porphyrazines (M = 2H(+), Mg2+, CU2+, Zn2+ and Co2+) substituted with eight (1-naphthylmethylthio) groups on the peripheral positions are described. Cyclic voltammetry and differential pulse voltammetry studies show that while metal-free, magnesium, zinc, and copper porphyrazine complexes give three ligand-based reductions and one ligand-based oxidation couple having diffusion controlled one-electron reversible character, cobalt porphyrazine gives both metal-based and ligand-based reduction and oxidation couples. Assignments of the redox couples were confirmed by spectroelectrochemical measurements. Distinctive voltammetric and spectroscopic changes during titration of the cobalt porphyrazine with soft metal Ag+ and Pd2+, show the metal sensing properties of the complexes. (c) 2007 Elsevier B.V. All rights reserved.
dc.identifier.doi10.1016/j.jelechem.2007.09.028
dc.identifier.eissn1873-2569
dc.identifier.issn1572-6657
dc.identifier.urihttps://hdl.handle.net/11424/229115
dc.identifier.wosWOS:000252600400010
dc.language.isoeng
dc.publisherELSEVIER SCIENCE SA
dc.relation.ispartofJOURNAL OF ELECTROANALYTICAL CHEMISTRY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectporphyrazine
dc.subjectspectroelectrochemistry
dc.subjectcyclic voltammetry
dc.subjectsilver
dc.subjectpalladium
dc.subjectmetal sensor
dc.subjectPHTHALOCYANINE
dc.subjectCOBALT
dc.subjectMANGANESE
dc.subjectBEHAVIOR
dc.subjectREDUCTION
dc.subjectCOMPLEXES
dc.subjectLIGANDS
dc.subjectBINDING
dc.subjectRINGS
dc.titleVoltammetric and spectroelectrochemical characterization of porphyrazines: Electrochemical metal sensor
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage240
oaire.citation.issue2
oaire.citation.startPage231
oaire.citation.titleJOURNAL OF ELECTROANALYTICAL CHEMISTRY
oaire.citation.volume612

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