Names | |
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IUPAC name Iron(II) diperchlorate | |
Other names
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Identifiers | |
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3D model (JSmol) | |
ChemSpider | |
ECHA InfoCard | 100.034.263 |
EC Number |
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PubChem CID | |
CompTox Dashboard (EPA) | |
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Properties | |
Fe(ClO4)2 | |
Molar mass | 254.75 g/mol |
Appearance | Green crystals |
Density | 2.15 g/cm3 |
Melting point | 100 °C (212 °F; 373 K) |
98 g/100 mL (25 °C) [1] | |
Structure [2] | |
Orthorhombic | |
Pmn21 | |
a = 7.79 Å, b = 13.48 Å, c = 5.24 Å | |
Hazards | |
GHS labelling: | |
Danger | |
H272, H315, H319, H335 | |
P210, P220, P221, P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P370+P378, P403+P233, P405, P501 | |
NFPA 704 (fire diamond) | |
Related compounds | |
Other cations | Manganese(II) perchlorate Cobalt(II) perchlorate Nickel(II) perchlorate |
Related compounds | Iron(III) perchlorate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Iron(II) perchlorate is the inorganic compound with the formula Fe(ClO4)2·6H2O. A green, water-soluble solid, it is produced by the reaction of iron metal with dilute perchloric acid followed by evaporation of the solution: [3]
Although the ferrous cation is a reductant and the perchlorate anion is a strong oxidant, in the absence of atmospheric oxygen, dissolved ferrous perchlorate is stable in aqueous solution because the electron transfer between both species Fe2+ and ClO−4 is hindered by severe kinetic limitations. Being a weak Lewis base, the perchlorate anion is a poor ligand for the aqueous Fe2+ and does not contribute to the electron transfer by favoring the formation of an inner sphere complex giving rise to a possible reorganisation of the activated complex. The resulting high activation energy prohibits a thermodynamically spontaneous redox reaction (∆Gr < 0).
However, in aqueous solution, and under air, iron(II) perchlorate slowly oxidizes to iron(III) oxyhydroxide. [4]
The hexahydrate consists of discreet hexa-aquo-iron(II) divalent cations and perchlorate anions. It crystallizes with an orthorhombic structure. [2] It has minor phase transitions at 245 and 336 K. [5]
In organic chemistry, iron(II) perchlorate can be used as a source of ferrous ions for the Fenton oxidation. [1]
Perchloric acid is a mineral acid with the formula HClO4. It is an oxoacid of chlorine. Usually found as an aqueous solution, this colorless compound is a stronger acid than sulfuric acid, nitric acid and hydrochloric acid. It is a powerful oxidizer when hot, but aqueous solutions up to approximately 70% by weight at room temperature are generally safe, only showing strong acid features and no oxidizing properties. Perchloric acid is useful for preparing perchlorate salts, especially ammonium perchlorate, an important rocket fuel component. Perchloric acid is dangerously corrosive and readily forms potentially explosive mixtures.
In chemistry, iron(II) refers to the element iron in its +2 oxidation state. The adjective ferrous or the prefix ferro- is often used to specify such compounds, as in ferrous chloride for iron(II) chloride (FeCl2). The adjective ferric is used instead for iron(III) salts, containing the cation Fe3+. The word ferrous is derived from the Latin word ferrum, meaning "iron".
An oxyanion, or oxoanion, is an ion with the generic formula A
xOz−
y. Oxyanions are formed by a large majority of the chemical elements. The formulae of simple oxyanions are determined by the octet rule. The corresponding oxyacid of an oxyanion is the compound H
zA
xO
y. The structures of condensed oxyanions can be rationalized in terms of AOn polyhedral units with sharing of corners or edges between polyhedra. The oxyanions adenosine monophosphate (AMP), adenosine diphosphate (ADP) and adenosine triphosphate (ATP) are important in biology.
Iron(III) chloride describes the inorganic compounds with the formula FeCl3(H2O)x. Also called ferric chloride, these compounds are some of the most important and commonplace compounds of iron. They are available both in anhydrous and in hydrated forms, which are both hygroscopic. They feature iron in its +3 oxidation state. The anhydrous derivative is a Lewis acid, while all forms are mild oxidizing agents. It is used as a water cleaner and as an etchant for metals.
Potassium ferrate is an inorganic compound with the formula K2FeO4. It is the potassium salt of ferric acid. Potassium ferrate is a powerful oxidizing agent with applications in green chemistry, organic synthesis, and cathode technology.
Chromium(III) chloride (also called chromic chloride) is an inorganic chemical compound with the chemical formula CrCl3. It forms several hydrates with the formula CrCl3·nH2O, among which are hydrates where n can be 5 (chromium(III) chloride pentahydrate CrCl3·5H2O) or 6 (chromium(III) chloride hexahydrate CrCl3·6H2O). The anhydrous compound with the formula CrCl3 are violet crystals, while the most common form of the chromium(III) chloride are the dark green crystals of hexahydrate, CrCl3·6H2O. Chromium chlorides find use as catalysts and as precursors to dyes for wool.
Pitting corrosion, or pitting, is a form of extremely localized corrosion that leads to the random creation of small holes in metal. The driving power for pitting corrosion is the depassivation of a small area, which becomes anodic while an unknown but potentially vast area becomes cathodic, leading to very localized galvanic corrosion. The corrosion penetrates the mass of the metal, with a limited diffusion of ions.
A solubility chart is a chart describing whether the ionic compounds formed from different combinations of cations and anions dissolve in or precipitate from solution.
Iron(III) nitrate, or ferric nitrate, is the name used for a series of inorganic compounds with the formula Fe(NO3)3.(H2O)n. Most common is the nonahydrate Fe(NO3)3.(H2O)9. The hydrates are all pale colored, water-soluble paramagnetic salts.
Iron shows the characteristic chemical properties of the transition metals, namely the ability to form variable oxidation states differing by steps of one and a very large coordination and organometallic chemistry: indeed, it was the discovery of an iron compound, ferrocene, that revolutionalized the latter field in the 1950s. Iron is sometimes considered as a prototype for the entire block of transition metals, due to its abundance and the immense role it has played in the technological progress of humanity. Its 26 electrons are arranged in the configuration [Ar]3d64s2, of which the 3d and 4s electrons are relatively close in energy, and thus it can lose a variable number of electrons and there is no clear point where further ionization becomes unprofitable.
Iron(II) carbonate, or ferrous carbonate, is a chemical compound with formula FeCO
3, that occurs naturally as the mineral siderite. At ordinary ambient temperatures, it is a green-brown ionic solid consisting of iron(II) cations Fe2+
and carbonate anions CO2−
3.
Ferroin is the chemical compound with the formula [Fe(o-phen)3]SO4, where o-phen is an abbreviation for 1,10-phenanthroline, a bidentate ligand. The term "ferroin" is used loosely and includes salts of other anions such as chloride.
The Schikorr reaction formally describes the conversion of the iron(II) hydroxide (Fe(OH)2) into iron(II,III) oxide (Fe3O4). This transformation reaction was first studied by Gerhard Schikorr. The global reaction follows:
Green rust is a generic name for various green crystalline chemical compounds containing iron(II) and iron(III) cations, the hydroxide (OH−
) anion, and another anion such as carbonate (CO2−
3), chloride (Cl−
), or sulfate (SO2−
4), in a layered double hydroxide (LDH) structure. The most studied varieties are the following:
A supporting electrolyte, in electrochemistry, according to an IUPAC definition, is an electrolyte containing chemical species that are not electroactive and which has an ionic strength and conductivity much larger than those due to the electroactive species added to the electrolyte. Supporting electrolyte is also sometimes referred to as background electrolyte, inert electrolyte, or inactive electrolyte.
Iron(II) selenate (ferrous selenate) is an inorganic compound with the formula FeSeO4. It has anhydrous and several hydrate forms. The pentahydrate has the structure, [Fe(H2O)4]SeO4•H2O, isomorphous to the corresponding iron(II) sulfate. Heptahydrate is also known, in form of unstable green crystalline solid.
Nickel(II) perchlorate is a collection of inorganic compounds with the chemical formula of Ni(ClO4)2(H2O)x. Its colors of these solids vary with the degree of hydration. For example, the hydrate forms cyan crystals, the pentahydrate forms green crystals, but the hexahydrate (Ni(ClO4)2·6H2O) forms blue crystals. Nickel(II) perchlorate hexahydrate is highly soluble in water and soluble in some polar organic solvents.
Cobalt(II) perchlorate is an inorganic chemical compound with the formula Co(ClO4)2·nH2O (n = 0,6). The pink anhydrous and red hexahydrate forms are both hygroscopic solids.
Manganese(II) perchlorate is an inorganic chemical compound with the formula Mn(ClO4)2. It forms a white-colored anhydrous and a rose-colored hexahydrate, both of which are hygroscopic. As a perchlorate, it is a strong oxidizing agent.
Transition metal perchlorate complexes are coordination complexes with one or more perchlorate ligands. Perchlorate can bind to metals through one, two, three, or all four oxygen atoms. Usually however, perchlorate is a counterion, not a ligand.