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Potassium ferrioxalate contains the iron(III) complex [Fe(C 2 O 4) 3] 3−. In chemistry, iron(III) or ferric refers to the element iron in its +3 oxidation state. Ferric chloride is an alternative name for iron(III) chloride (FeCl 3). The adjective ferrous is used instead for iron(II) salts, containing the cation Fe 2+.
Iron(III) oxide is a product of the oxidation of iron. It can be prepared in the laboratory by electrolyzing a solution of sodium bicarbonate, an inert electrolyte, with an iron anode: 4 Fe + 3 O 2 + 2 H 2 O → 4 FeO(OH) The resulting hydrated iron(III) oxide, written here as FeO(OH), dehydrates around 200 °C. [18] [19] 2 FeO(OH) → Fe 2 O 3 ...
The formation of Fe(III)-EDTA (FeY) − can be described as follows: FeSO 4 ∙7H 2 O + K 2 H 2 Y + 1/4 O 2 → K[FeY(H 2 O)]. H 2 O + KHSO 4 + 5.5 H 2 O (1) [8]. Iron chelate has also been used as a bait in the chemical control of slugs, snails and slaters in agriculture in Australia and New Zealand.
The iron compounds produced on the largest scale in industry are iron(II) sulfate (FeSO 4 ·7H 2 O) and iron(III) chloride (FeCl 3). The former is one of the most readily available sources of iron(II), but is less stable to aerial oxidation than Mohr's salt ((NH 4) 2 Fe(SO 4) 2 ·6H 2 O). Iron(II) compounds tend to be oxidized to iron(III ...
Iron(II) complexes are less stable than iron(III) complexes but the preference for O-donor ligands is less marked, so that for example [Fe(NH 3) 6] 2+ is known while [Fe(NH 3) 6] 3+ is not. They have a tendency to be oxidized to iron(III) but this can be moderated by low pH and the specific ligands used. [72]
Ferric oxalate, also known as iron(III) oxalate, refers to inorganic compounds with the formula Fe 2 (C 2 O 4) 3 (H 2 O) x but could also refer to salts of [Fe(C 2 O 4) 3] 3-. Fe 2 (C 2 O 4 ) 3 (H 2 O) x are coordination polymers with varying degrees of hydration.
structure of the cation called basic iron acetate as determined from X-ray crystallography [4] Basic iron acetate forms on treating aqueous solutions of iron(III) sources with acetate salts. It is slowly soluble in water and poorly soluble in acetic acid. [5] A typical precursor is freshly precipitated iron oxide/hydroxide, which is halide-free ...
ion in ferric citrate (as in many iron(III) carboxylates) is reduced by exposure to light, [8] especially blue and ultraviolet, to Fe 2+ (ferrous) ion with concomitant oxidation of the carboxyl group adjacent to the hydroxyl, yielding carbon dioxide and acetonedicarboxylate: 2 Fe 3+ + R 2-C(OH)-CO − 2 → 2 Fe 2+ + R 2-C=O + H + + CO 2