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Electrochemical disproportionation in new ruthenium (II) nitro complexes with 2,4,6-tris(2-pyridyl)-1,3,5-triazine detected by IR spectroelectrochemistry with an OTTLE cell
Affiliation:1. Department of Chemistry, University of North Bengal, Darjeeling 734013, India;2. Department of Chemical Sciences, Indian Institute of Science Education and Research, Mohali, Sector 81, Knowledge City, S. A. S. Nagar, Manauli PO, Mohali, Punjab 140306, India;3. Department of Chemistry, Dinabandhu Andrews College, Kolkata 700084, India;1. Depto. Química Analítica, Facultad de Ciencias Químicas, Benemérita Universidad Autónoma de Puebla, Puebla 72570, Mexico;2. Instituto de Física, Benemérita Universidad Autónoma de Puebla, Apartado postal J-48, Puebla 72570, Mexico
Abstract:The syntheses and characterization of new nitro complexes of Ru(II) with 2,4,6-tris(2-pyridyl)-1,3,5-triazine (tptz) and different substituted bipyridines are reported. A disproportionation reaction can occur after applying an oxidation potential corresponding to the couple RuII/RuIII forming the nitrate and the nitrosyl complexes, which were detected by cyclic voltammetry. This reaction was confirmed by IR-spectroelectrochemistry with an OTTLE cell, for the first time. Additionally, for 2,2′-bipyridine we have obtained as ClO4 salt a new nitrosyl-complex which presents an elevated IR stretching frequency.
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