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Concise synthesis, electrochemistry and spectroelectrochemistry of phthalocyanines having triazole functionality

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dc.creator Ozalp-Yaman, Seniz
dc.creator TANYELİ, CİHANGİR
dc.creator Karaca, Huseyin
dc.creator Sezer, Serdar
dc.date 2014-04-09T21:00:00Z
dc.date.accessioned 2020-10-06T10:32:44Z
dc.date.available 2020-10-06T10:32:44Z
dc.identifier 76b103e8-afd7-434d-b62b-9b3dcf41325c
dc.identifier 10.1016/j.poly.2014.01.037
dc.identifier https://avesis.sdu.edu.tr/publication/details/76b103e8-afd7-434d-b62b-9b3dcf41325c/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/63760
dc.description The synthesis of novel metallophthalocyanines (M = Zn, Ni) bearing substituted benzyl protected 1,2,3-triazole moieties at peripheral positions is described for the first time via direct cyclotetramerization. These complexes have been characterized by a combination of FT-IR, H-1 NMR, HRMS and UVVis spectroscopy techniques and all the new compounds are highly soluble in most common organic solvents. In addition, the electrochemical and electrochromic behaviors of the complexes are investigated. Cyclic voltammetry and differential pulse voltammetry measurements demonstrate ligand base oxidations and reductions for both the Zn(II) and Ni(II) phthalocyanines by the transfer of one electron in each electrochemical step. The redox couples are identified in situ by monitoring the electronic absorption spectral changes during the electrolysis.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Concise synthesis, electrochemistry and spectroelectrochemistry of phthalocyanines having triazole functionality
dc.type info:eu-repo/semantics/article


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