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Novel `synthetic metals' based on symmetrically tetrasubstituted nickel phthalocyanines
Affiliation:1. Centro de Nanociencias Aplicadas (CENAP), Doctorado de Fisicoquímica Molecular Universidad Andres Bello, Av. República 275, Santiago 8370146, Chile;2. Facultad de Quimica y Biología, Departamento de Quimica de los Materiales, Universidad de Santiago de Chile, Casilla 40, Correo 33, Santiago 9170022, Chile;3. Facultad Ciencias de la Salud, Universidad Autónoma de Chile, Av. Pedro de Valdivia 641, Chile;1. Department of Chemistry, Faculty of Science, Karadeniz Technical University, 61080 Trabzon, Turkey;2. Department of Chemistry, Faculty of Science, Istanbul Technical University, Maslak, Istanbul, Turkey;3. Department of Chemical Engineering, Engineering Faculty, Marmara University, 34722 Göztepe, Istanbul, Turkey;1. Faculty of Chemistry, Jagiellonian University, Ingardena 3, 30-060 Kraków, Poland;2. Department of Biophysics, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Gronostajowa 7, 30-387 Krakow, Poland;1. College of Chemistry & Materials, Fujian Province Key Laboratory of Polymer Materials, Fujian Normal University, Fuzhou, China;2. Provincial Clinical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, China;3. Fujian Institute of Research on the Structure of Matter, Chinese Academic of Sciences, Fuzhou, China;4. Key Laboratory of Optoelectronic Science and Technology for Medicine of Ministry of Education, Fujian Normal University, Fuzhou, China;1. Department of Chemistry, University of Pretoria, Pretoria 0002, South Africa;2. Department of Pure and Industrial Chemistry, University of Nigeria, 410001 Nsukka, Nigeria;3. Energy Materials, Materials Science and Manufacturing, Council for Scientific & Industrial Research (CSIR), Pretoria 0001, South Africa
Abstract:Nickel(II) 2,9,16,23-tetrasubstituted phthalocyanines, NiPTX (where X=–OH, –NO2, –NH2 and –SO3H) were synthesized in pure state and doped with iodine. Elemental analysis, UV-Vis, infrared, X-ray diffraction, magnetic susceptibility and TGA studies were used to investigate the effects of iodine doping as well as substituents on the properties of the complexes. The electrical conductivity of nickel phthalocyanine derivatives found to depend on the nature of the substituents and showed ∼103–105 times increased electrical conductivity in comparison to parent nickel phthalocyanine. Further, the substitution and iodine doping show remarkably very high improved electrical conductivity nearly 1011 times the electrical conductivity of nickel phthalocyanine.
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