Tetrachloroferrate

Last updated
Tetrachloroferrate
Tetrachloroferrate.svg
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
26231
PubChem CID
  • InChI=1S/4ClH.Fe/h4*1H;/q;;;;+3/p-4
    Key: HCQLFHJKDCJBSQ-UHFFFAOYSA-J
  • Cl[Fe-](Cl)(Cl)Cl
Properties
Cl4Fe−1
Molar mass 197.65 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Tetrachloroferrate is the polyatomic ion having chemical formula FeCl4. The metallate can be formed when ferric chloride (FeCl3) abstracts a chloride ion from various other chloride salts. [1] The resulting tetrachloroferrate salts are typically soluble in non-polar solvents. The tetrachloroferrate anion, with iron(III) in the center, has tetrahedral geometry. [2] It is useful as a non-coordinating anion comparable to perchlorate. [3] Several organoammonium salts have been studied for their novel material properties. 1-Butyl-3-methylimidazolium tetrachloroferrate is one of several ionic liquids that are magnetic. [4] Trimethylchloromethylammonium tetrachloroferrate is a plastic crystal that can behave as a molecular switch in response to several different types of inputs. [5]

Related Research Articles

In chemistry, a salt is a chemical compound consisting of an ionic assembly of positively charged cations and negatively charged anions, which results in a compound with no net electric charge. A common example is table salt, with positively charged sodium ions and negatively charged chloride ions.

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 of an atom in a chemical compound. Conceptually, the oxidation state may be positive, negative or zero. While fully ionic bonds are not found in nature, many bonds exhibit strong ionicity, making oxidation state a useful predictor of charge.

An electrolyte is a medium containing ions that is electrically conducting through the movement of those ions, but not conducting electrons. This includes most soluble salts, acids, and bases dissolved in a polar solvent, such as water. Upon dissolving, the substance separates into cations and anions, which disperse uniformly throughout the solvent. Solid-state electrolytes also exist. In medicine and sometimes in chemistry, the term electrolyte refers to the substance that is dissolved.

<span class="mw-page-title-main">Iron(III)</span> The element iron in its +3 oxidation state

In chemistry, iron(III) refers to the element iron in its +3 oxidation state. In ionic compounds (salts), such an atom may occur as a separate cation (positive ion) denoted by Fe3+.

<span class="mw-page-title-main">Ionic compound</span> Chemical compound involving ionic bonding

In chemistry, an ionic compound is a chemical compound composed of ions held together by electrostatic forces termed ionic bonding. The compound is neutral overall, but consists of positively charged ions called cations and negatively charged ions called anions. These can be simple ions such as the sodium (Na+) and chloride (Cl) in sodium chloride, or polyatomic species such as the ammonium (NH+
4
) and carbonate (CO2−
3
) ions in ammonium carbonate. Individual ions within an ionic compound usually have multiple nearest neighbours, so are not considered to be part of molecules, but instead part of a continuous three-dimensional network. Ionic compounds usually form crystalline structures when solid.

Iron(III) chloride describes the inorganic compounds with the formula FeCl3(H2O)x. Also called ferric chloride, these compounds are available both in anhydrous and hydrated forms which are both hygroscopic. They are common sources of iron in its +3 oxidation state. The anhydrous derivative is a Lewis acid, while the hydrate is a mild oxidizing agent. It is used as a water cleaner and as an etchant for metals.

<span class="mw-page-title-main">Ionic liquid</span> Salt in the liquid state

An ionic liquid (IL) is a salt in the liquid state. In some contexts, the term has been restricted to salts whose melting point is below a specific temperature, such as 100 °C (212 °F). While ordinary liquids such as water and gasoline are predominantly made of electrically neutral molecules, ionic liquids are largely made of ions. These substances are variously called liquid electrolytes, ionic melts, ionic fluids, fused salts, liquid salts, or ionic glasses.

1-Butyl-3-methylimidazolium tetrachloroferrate is a magnetic ionic liquid. It can be obtained from 1-butyl-3-methylimidazolium chloride and ferric chloride. It has quite low water solubility.

<span class="mw-page-title-main">Phosphonium</span> Family of polyatomic cations containing phosphorus

In chemistry, the term phosphonium describes polyatomic cations with the chemical formula PR+
4
. These cations have tetrahedral structures. The salts are generally colorless or take the color of the anions.

In chemistry, a phase-transfer catalyst or PTC is a catalyst that facilitates the transition of a reactant from one phase into another phase where reaction occurs. Phase-transfer catalysis is a special form of catalysis and can act through homogeneous catalysis or heterogeneous catalysis methods depending on the catalyst used. Ionic reactants are often soluble in an aqueous phase but insoluble in an organic phase in the absence of the phase-transfer catalyst. The catalyst functions like a detergent for solubilizing the salts into the organic phase. Phase-transfer catalysis refers to the acceleration of the reaction upon the addition of the phase-transfer catalyst.

<span class="mw-page-title-main">Tetramethylammonium hydroxide</span> Chemical compound

Tetramethylammonium hydroxide (TMAH or TMAOH) is a quaternary ammonium salt with molecular formula N(CH3)4+ OH. It is commonly encountered in form of concentrated solutions in water or methanol. TMAH in solid state and its aqueous solutions are all colorless, but may be yellowish if impure. Although TMAH has virtually no odor when pure, samples often have a strong fishy smell due to presence of trimethylamine which is a common impurity. TMAH has several diverse industrial and research applications.

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.

An alkalide is a chemical compound in which alkali metal atoms are anions with a charge or oxidation state of −1. Until the first discovery of alkalides in the 1970s, alkali metals were known to appear in salts only as cations with a charge or oxidation state of +1. These types of compounds are of theoretical interest due to their unusual stoichiometry and low ionization potentials. Alkalide compounds are chemically related to the electrides, salts in which trapped electrons are effectively the anions.

<span class="mw-page-title-main">Hexafluorophosphate</span> Anion with the chemical formula PF6–

Hexafluorophosphate is an anion with chemical formula of [PF6]. It is an octahedral species that imparts no color to its salts. [PF6] is isoelectronic with sulfur hexafluoride, SF6, and the hexafluorosilicate dianion, [SiF6]2−, and hexafluoroantimonate [SbF6]. In this anion, phosphorus has a valence of 5. Being poorly nucleophilic, hexafluorophosphate is classified as a non-coordinating anion.

<span class="mw-page-title-main">Chloroauric acid</span> Chemical compound

Chloroauric acid is an inorganic compound with the chemical formula H[AuCl4]. It forms hydrates H[AuCl4nH2O. Both the trihydrate and tetrahydrate are known. Both are orange-yellow solids consisting of the planar [AuCl4] anion. Often chloroauric acid is handled as a solution, such as those obtained by dissolution of gold in aqua regia. These solutions can be converted to other gold complexes or reduced to metallic gold or gold nanoparticles.

In chemistry, ion association is a chemical reaction whereby ions of opposite electric charge come together in solution to form a distinct chemical entity. Ion associates are classified, according to the number of ions that associate with each other, as ion pairs, ion triplets, etc. Ion pairs are also classified according to the nature of the interaction as contact, solvent-shared or solvent-separated. The most important factor to determine the extent of ion association is the dielectric constant of the solvent. Ion associates have been characterized by means of vibrational spectroscopy, as introduced by Niels Bjerrum, and dielectric-loss spectroscopy.

<span class="mw-page-title-main">Iron(II)</span> The element iron in its +2 oxidation state

In chemistry, iron(II) refers to the element iron in its +2 oxidation state. In ionic compounds (salts), such an atom may occur as a separate cation (positive ion) denoted by Fe2+.

<span class="mw-page-title-main">Tetrachloronickelate</span> Class of chemical compounds

Tetrachloronickelate is the metal complex with the formula [NiCl4]2−. Salts of the complex are available with a variety of cations, but a common one is tetraethylammonium.

<span class="mw-page-title-main">Transition metal chloride complex</span> Coordination complex

In chemistry, a transition metal chloride complex is a coordination complex that consists of a transition metal coordinated to one or more chloride ligand. The class of complexes is extensive.

A chloroanion is an anion that contains an element and chlorine atoms. They are also known as complex chlorides. They can occur in salts, or in solution, but not as pure acids. They mostly can be considered as chlorometallates which are a subclass of halometallates.

References

  1. Cook, Charles M. Jr.; Dunn, Wendell E. Jr. (1961). "The Reaction of Ferric Chloride with Sodium and Potassium Chlorides". J. Phys. Chem. 65 (9): 1505–1511. doi:10.1021/j100905a008.
  2. Lutz, Martin; Huang, Yuxing; Moret, Marc-Etienne; Klein Gebbink, Robertus J. M. (2014). "Phase Transitions and Twinned Low-Temperature Structures of Tetraethylammonium Tetrachloridoferrate(III)". Acta Crystallographica Section C. 70 (5): 470–476. doi:10.1107/S2053229614007955. hdl: 1874/307900 . PMID   24816016.
  3. Golding, Raymund M.; Harris, CM; Jessop, KJ; Tennant, William C. (1972). "Oxidation of dithiocarbamato metal complexes". Australian Journal of Chemistry. 25 (12): 2567–2576. doi:10.1071/CH9722567.
  4. Hayashi, Satoshi; Saha, Satyen; Hamaguchi, Hiro-o (2006). "A new class of magnetic fluids: bmim[FeCl4] and nbmim[FeCl4] ionic liquids". IEEE Transactions on Magnetics . 42 (1): 12–14. Bibcode:2006ITM....42...12H. doi:10.1109/TMAG.2005.854875. S2CID   42347833.
  5. Li, Dong; Zhao, Xue-Mei; Zhao, Hai-Xia; Long, La-Sheng; Zheng, Lan-Sun (2019). "Coexistence of Magnetic-Optic-Electric Triple Switching and Thermal Energy Storage in a Multifunctional Plastic Crystal of Trimethylchloromethyl Ammonium Tetrachloroferrate(III)". Inorg. Chem. 58 (1): 655–662. doi:10.1021/acs.inorgchem.8b02835. PMID   30576116. S2CID   58631842.