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dc.contributor.authorSener, Sevil
dc.contributor.authorSelcuki, Nursel Acar
dc.contributor.authorDumludag, Fatih
dc.contributor.authorSalih, Bekir
dc.contributor.authorBekaroglu, Ozer
dc.date.accessioned2020-08-30T20:06:59Z
dc.date.available2020-08-30T20:06:59Z
dc.date.issued2019
dc.identifier.citationSener, S., Selcuki, N. A., Dumludag, F., Salih, B., & Bekaroglu, O. (2019). Synthesis, Conductivity, and Impedance Studies on Metallophthalocyanines Formed Across Adjacent Rings. EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, (6), 770–779. https://doi.org/10.1002/ejic.201801209en_US
dc.identifier.issn1434-1948
dc.identifier.issn1099-0682
dc.identifier.urihttps://doi.org/10.1002/ejic.201801209
dc.identifier.urihttps://hdl.handle.net/20.500.12713/667
dc.descriptionSelcuki, Nursel Acar/0000-0001-9292-0637; Bekaroglu, Ozer ---/0000-0002-9249-2385; SENER, Sevil/0000-0002-4766-9727en_US
dc.descriptionWOS: 000458689800005en_US
dc.descriptionBekaroglu, Ozer (isu author)
dc.description.abstractThe synthesis and characterization of Co-II, Zn-II, and Ni-II phthalocyanines (Pcs) 4, 5, and 6, respectively, containing two bis[2-(4-hydroxyphenyl)-2-propyl]benzene groups formed across adjacent rings at the peripheral positions are described. The Pcs were synthesized by cyclotetramerization of the previously prepared precursor 4,4 '-bis[1,3-propylbenzene-2-p-phenoxy]phthalonitrile (3) in the presence of metal salt in boiling dry DMF under a dry nitrogen atmosphere. Elemental analysis, UV-Vis, FT-IR, and H-1-NMR spectroscopy, as well as MALDI-TOF mass spectrometry techniques were used for the characterization of 4. Conductivity (dc and ac) and impedance spectroscopy (IS) measurements were performed on the films of 5 and 6 between the temperatures 293 and 523 K and frequencies 40 and100 kHz. The dc conductivity values were calculated as 2.11 x 10-(10), 3.48 x 10-(10), and 1.90 x 10-(10) S/cm for the films of 4, 5, and 6, respectively, at room temperature. Activation energy values of the films were also calculated. Conductivity (ac) results suggest that the dominant charge transport mechanisms can be explained by the hopping model depending on temperature and frequency range. From impedance spectra and Cole-Cole plots, the relaxation time in the Debye dispersion relation is considered as a distribution of relaxation time values rather than as a single relaxation time. To elucidate the structural, spectroscopic, and bonding properties of the obtained compounds, DFT/TD-DFT calculations were performed.en_US
dc.description.sponsorshipScientific Research Commission of Marmara University (BAPKO)Marmara University [FEN-BGS-290506-0114]; Turkish Academy of Sciences (TUBA)Turkish Academy of Sciencesen_US
dc.description.sponsorshipThe authors gratefully acknowledge financial support by the Scientific Research Commission of Marmara University (BAPKO Project No: FEN-BGS-290506-0114), the Turkish Academy of Sciences (TUBA), and computer time on the FenCluster provided by the Ege University Faculty of Science and TUBITAK-ULAKBIM Truba Resources.en_US
dc.language.isoengen_US
dc.publisherWiley-V C H Verlag Gmbhen_US
dc.relation.isversionof10.1002/ejic.201801209en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectConductivityen_US
dc.subjectDensity Functional Calculationsen_US
dc.subjectElectrical Characterizationen_US
dc.subjectPhthalocyaninesen_US
dc.subjectCobalten_US
dc.subjectNickelen_US
dc.subjectZincen_US
dc.titleSynthesis, conductivity, and ımpedance studies on metallophthalocyanines formed across adjacent ringsen_US
dc.typearticleen_US
dc.contributor.departmentİstinye Üniversitesi, Eczacılık Fakültesi, Eczacılık Temel Bilimleri Bölümüen_US
dc.contributor.authorID0000-0002-9249-2385en_US
dc.contributor.institutionauthorBekaroglu, Ozeren_US
dc.identifier.issue6en_US
dc.identifier.startpage770en_US
dc.identifier.endpage779en_US
dc.relation.journalEuropean Journal of Inorganic Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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