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Chemical assembly of the heteronuclear pivalate complex with the LiI and FeIII ions
Authors:I.?А.?Lutsenko  author-information"  >  author-information__contact u-icon-before"  >  mailto:irinalu@rambler.ru"   title="  irinalu@rambler.ru"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,М.?А.?Kiskin,G.?G.?Alexandrov,V.?K.?Imshennik,Yu.?V.?Maksimov,A.?V.?Khoroshilov,A.?S.?Goloveshkin,А.?А.?Sidorov,I.?L.?Eremenko
Affiliation:1.N. S. Kurnakov Institute of General and Inorganic Chemistry,Russian Academy of Sciences,Moscow,Russian Federation;2.N. N. Semenov Institute of Chemical Physics,Russian Academy of Sciences,Moscow,Russian Federation;3.A. N. Nesmeyanov Institute of Organoelement Compounds,Russian Academy of Sciences,Moscow,Russian Federation
Abstract:The heteronuclear complex [Fe4Li2(O)2(Piv)10(H2O)2] (1, Piv is the pivalic acid anion) was obtained by refluxing FeIII pivalates with LiI pivalates in toluene and isolated as the 1?PhCH3 solvate with a toluene molecule. According to X-ray diffraction data, complex 1 contains the {Fe4Li2O2} core. The Mössbauer spectroscopy data indicate that the core comprises para magnetic FeIII ions in the high-spin state located in the symmetric octahedral environment of oxygen atoms. Thermolysis of 1 studied by simultaneous thermal analysis demonstrated thermal stability of the complex up to 225 °С. The main end product of thermolysis at 600 °С is the mixed oxide LiFe5O8.
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