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Sodium ferrocyanide is the sodium salt of the coordination compound of formula [Fe(CN) 6] 4−. In its hydrous form, Na 4 Fe(CN) 6 · H 2 O (sodium ferrocyanide decahydrate), it is sometimes known as yellow prussiate of soda. It is a yellow crystalline solid that is soluble in water and insoluble in alcohol. The yellow color is the color of ...
Ferrocyanide is the name of the anion [Fe 6] 4−. Salts of this coordination complex give yellow solutions. It is usually available as the salt potassium ferrocyanide, which has the formula K 4 Fe(CN) 6. [Fe(CN) 6] 4− is a diamagnetic species, featuring low-spin iron(II) center in an octahedral ligand environment.
Cyanogen azide is a chemical compound with the chemical formula C N 4, or more precisely − N=N + =N−C≡N. It is an azide compound of carbon and nitrogen. It is an oily, colourless liquid at room temperature. [2] It is a highly explosive chemical that is soluble in most organic solvents, and normally handled in dilute solution in this form.
2 K 4 [Fe(CN) 6] + Cl 2 → 2 K 3 [Fe(CN) 6] + 2 KCl. This reaction can be used to remove potassium hexacyanidoferrate(II) from a solution. [citation needed] A famous reaction involves treatment with ferric salts, most commonly Iron(III) chloride, to give Prussian blue. In the reaction with Iron(III) chloride, producing Potassium chloride as a ...
Prussian blue (also known as Berlin blue, Brandenburg blue, Parisian and Paris blue) is a dark blue pigment produced by oxidation of ferrous ferrocyanide salts. It has the chemical formula Fe 3+ 4 [Fe 2+ 6] 3.
The iron is low spin and easily reduced to the related ferrocyanide ion [Fe(CN) 6] 4−, which is a ferrous (Fe 2+) derivative. This redox couple is reversible and entails no making or breaking of Fe–C bonds: [Fe(CN) 6] 3− + e − ⇌ [Fe(CN) 6] 4−. This redox couple is a standard in electrochemistry.
In chemistry, the oxidation state, or oxidation number, is the hypothetical charge of an atom if all of its bonds to other atoms were fully ionic. It describes the degree of oxidation (loss of electrons ) of an atom in a chemical compound .
Typical nitrile ligands are acetonitrile, propionitrile, and benzonitrile.The structures of [Ru(NH 3) 5 (NCPh)] n+ have been determined for the 2+ and 3+ oxidation states. Upon oxidation the Ru-NH 3 distances contract and the Ru-NCPh distances elongate, consistent with amines serving as pure-sigma donor ligands and nitriles functioning as pi-acceptors.