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Thermal decomposition of dinuclear complexes LM(μ-OOCR)4ML (L is α-substituted pyridine)
Authors:I. G. Fomina  Zh. V. Dobrokhotova  G. G. Aleksandrov  M. A. Kiskin  M. A. Bykov  V. N. Ikorskii  V. M. Novotortsev  I. L. Eremenko
Affiliation:1.N. S. Kurnakov Institute of General and Inorganic Chemistry,Russian Academy of Sciences,Moscow,Russian Federation;2.Department of Chemistry,M. V. Lomonosov Moscow State University,Moscow,Russian Federation;3.International Tomography Center,Siberian Branch of the Russian Academy of Sciences,Novosibirsk,Russian Federation
Abstract:The solid-state thermal decomposition of the dinuclear pivalate complexes LM(μ-OOCR)4ML, both those synthesized earlier (M = MnII, FeII, or CoII; L = 2,6-(NH2)2C5H3N)) and new complexes (M = CuII; L = 2,6-(NH2)2C5H3N or (2-NH2)(6-CH3)C5H3N), was studied by differential scanning calorimetry and thermogravimetry. The decomposition of the CoII complexes is accompanied by the aggregation to form the volatile octanuclear complex Co84-O)2n-OOCCMe3)12 (n = 2 or 3), whereas the thermolysis of the MnII, FeII, and CuII complexes is destructive, the phase composition of the decomposition products being substantially dependent on the nature of metal and the α substituent R in the apical organic ligand.
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