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On the Existence of Intercalation Compound of Boron Nitride with Ferric Chloride
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Mercury oxidation in vitro by ferric compounds
Archives of Toxicology, 1982Among the ferric compounds studied, cytochrome C, methemoglobin, lactoperoxidase, ferritin and ferric ion, in addition to catalase, had the ability to oxidize metallic mercury in the presence of hydrogen peroxide. On the other hand, hematin, the active center of catalase, did not oxidize metallic mercury.
M, Ogata +3 more
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Interactions of Ferric Ions with Olive Oil Phenolic Compounds
Journal of Agricultural and Food Chemistry, 2005The ferric complexing capacity of four phenolic compounds, occurring in olives and virgin olive oil, namely, oleuropein, hydroxytyrosol, 3,4-dihydroxyphenylethanol-elenolic acid (3,4-DHPEA-EA), and 3,4-dihydroxyphenylethanol-elenolic acid dialdehyde (3,4-DHPEA-EDA), and their stability in the presence of ferric ions were studied.
Fátima, Paiva-Martins +1 more
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The Absorption Spectra of Ferric Compounds. I. The Ferric Chloride—Phenol Reaction
Journal of the American Chemical Society, 1934Edward F. Wesp, Wallace R. Brode
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Photoreduction of Ferric Compounds in Aqueous Solution
The Journal of Physical Chemistry, 1955J. H. Baxendale, N. K. Bridge
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Ferric iodide as a nonexistent compound
Inorganic Chemistry, 1990Reactivite et stabilite du compose FeI 3 : formation de FeI 4 − , metastabilite sous rayonnement visible et effet de l'oxygene moleculaire ou des halogenures d'alkyles en solution.
K. B. Yoon, J. K. Kochi
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Sternheimer Quadrupole Factors in Ferric Compounds
physica status solidi (b), 1982AbstractExpressions for the quadrupole shielding (antishielding) factors corresponding to various types of electronic charge distributions in a solid complex are obtained by means of Sternheimer's perturbation‐numerical method generalized for the two‐centre case.
E. Z. Liverts, A. K. Zhetbaev
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Solubilities and stabilities of ferric arsenate compounds
Hydrometallurgy, 1989Basic ferric arsenates precipitated from hydrometallurgical liquors by hydrolysis are shown to be very insoluble over a range of pHs. The stability range (solubilities
E. Krause, V.A. Ettel
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