Identifiers | |
---|---|
3D model (JSmol) |
|
PubChem CID |
|
| |
| |
Properties | |
Co(OCN)2 | |
Molar mass | 142.97 g/mol |
Related compounds | |
Other anions | Cobalt(II) thiocyanate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Cobalt(II) cyanate is the hypothetical inorganic compound with the formula Co(OCN)2.
The simple cobalt(II) cyanate has not been proven to be made. However, the tetraisocyanatocobalt(II) ion (Co(NCO)42-) is known and its blue color and is used as a qualitative test for cobalt(II) ions.
Cobalt(II) cyanate was claimed to have been produced in 1952 by carefully heating pyridine cobalt(II) cyanate under vacuum. The nature of the compound produced has not been elucidated by X-ray diffraction. [1]
In contrast, the tetraisocyanatocobalt(II) ion (Co(NCO)42-) has been identified by X-ray crystallography and is widely known. [2] After being first produced in 1871, it has been used as a qualitative test for cobalt(II). [3]
Other cyanate complexes of cobalt have been discovered, such as tetrakis(pyridine)cobalt(II) cyanate. [4]
Multiple compounds of the related tetracyanatocobaltate(II) has been structurally elucidated, such as [Co(C5H5)2]2[Co(NCO)4]. All of these complexes have an intense blue color. [2] [5]
Potassium tetraisocyanatocobaltate(II) has been produced by the reaction of potassium cyanate and cobalt(II) nitrate: [6]
Tetracyanatocobaltate(II) salts with other counterions, such as cobaltcenium [Co(C5H5)]+ and EMIM are known. [2]
Cobalt(II) cyanate complexes have been produced by the addition of potassium cyanate to a soluble cobalt salt, such as cobalt(II) chloride, followed by the addition of the complexing agent, such as pyridine, bipyridine, [7] quinoline, and 2,6-dimethylpyrazine. [8]
Although the simple cyanate is unknown, the structure of the tetracyanatocobaltate(II) ion has been elucidated. The [Co(NCO)4]2- ion consists of a nitrogen-bonded tetrahederal central cobalt atom. The cobalt-nitrogen bond length is about 1.96 Å. [2]
Carbon compounds are defined as chemical substances containing carbon. More compounds of carbon exist than any other chemical element except for hydrogen. Organic carbon compounds are far more numerous than inorganic carbon compounds. In general bonds of carbon with other elements are covalent bonds. Carbon is tetravalent but carbon free radicals and carbenes occur as short-lived intermediates. Ions of carbon are carbocations and carbanions are also short-lived. An important carbon property is catenation as the ability to form long carbon chains and rings.
A metallocene is a compound typically consisting of two cyclopentadienyl anions (C
5H−
5, abbreviated Cp) bound to a metal center (M) in the oxidation state II, with the resulting general formula (C5H5)2M. Closely related to the metallocenes are the metallocene derivatives, e.g. titanocene dichloride or vanadocene dichloride. Certain metallocenes and their derivatives exhibit catalytic properties, although metallocenes are rarely used industrially. Cationic group 4 metallocene derivatives related to [Cp2ZrCH3]+ catalyze olefin polymerization.
Thiocyanates are salts containing the thiocyanate anion [SCN]−. [SCN]− is the conjugate base of thiocyanic acid. Common salts include the colourless salts potassium thiocyanate and sodium thiocyanate. Mercury(II) thiocyanate was formerly used in pyrotechnics.
Pseudohalogens are polyatomic analogues of halogens, whose chemistry, resembling that of the true halogens, allows them to substitute for halogens in several classes of chemical compounds. Pseudohalogens occur in pseudohalogen molecules, inorganic molecules of the general forms Ps–Ps or Ps–X, such as cyanogen; pseudohalide anions, such as cyanide ion; inorganic acids, such as hydrogen cyanide; as ligands in coordination complexes, such as ferricyanide; and as functional groups in organic molecules, such as the nitrile group. Well-known pseudohalogen functional groups include cyanide, cyanate, thiocyanate, and azide.
In chemistry, linkage isomerism or ambidentate isomerism is a form of isomerism in which certain coordination compounds have the same composition but differ in their metal atom's connectivity to a ligand.
The cyanate ion is an anion with the chemical formula OCN−. It is a resonance of three forms: [O−−C≡N] (61%) ↔ [O=C=N−] (30%) ↔ [O+≡C−N2−] (4%).
A salt metathesis reaction is a chemical process involving the exchange of bonds between two reacting chemical species which results in the creation of products with similar or identical bonding affiliations. This reaction is represented by the general scheme:
In chemical nomenclature, the IUPAC nomenclature of inorganic chemistry is a systematic method of naming inorganic chemical compounds, as recommended by the International Union of Pure and Applied Chemistry (IUPAC). It is published in Nomenclature of Inorganic Chemistry. Ideally, every inorganic compound should have a name from which an unambiguous formula can be determined. There is also an IUPAC nomenclature of organic chemistry.
Sodium hexanitritocobaltate(III) is an inorganic compound with the formula Na3[Co(NO2)6]. The anion of this yellow-coloured salt consists of the transition metal nitrite complex [Co(NO2)6]3−. It was a reagent for the qualitative test for potassium and ammonium ions.
Mercury(II) thiocyanate is an inorganic chemical compound, the coordination complex of Hg2+ and the thiocyanate anion. It is a white powder. It will produce a large, winding "snake" when ignited, an effect known as the Pharaoh's serpent.
Cobalt nitrate is the inorganic compound with the formula Co(NO3)2.xH2O. It is cobalt(II)'s salt. The most common form is the hexahydrate Co(NO3)2·6H2O, which is a red-brown deliquescent salt that is soluble in water and other polar solvents.
In chemistry, an ate complex is a salt formed by the reaction of a Lewis acid with a Lewis base whereby the central atom increases its valence and gains a negative formal charge..
Cobalt(II) thiocyanate is an inorganic compound with the formula Co(SCN)2. The anhydrous compound is a coordination polymer with a layered structure. The trihydrate, Co(SCN)2(H2O)3, is a isothiocyanate complex used in the cobalt thiocyanate test (or Scott test) for detecting cocaine. The test has been responsible for widespread false positives and false convictions.
Chloro(pyridine)cobaloxime is a coordination compound containing a CoIII center with octahedral coordination. It has been considered as a model compound of vitamin B12 for studying the properties and mechanism of action of the vitamin. It belongs to a class of bis(dimethylglyoximato)cobalt(III) complexes with different axial ligands, called cobaloximes. Chloro(pyridine)cobaloxime is a yellow-brown powder that is sparingly soluble in most solvents, including water.
Silver cyanate is the cyanate salt of silver. It can be made by the reaction of potassium cyanate with silver nitrate in aqueous solution, from which it precipitates as a solid.
Diphenyl-2-pyridylmethane is a triaryl organic compound that has been used to selectively extract specific metal ions into organic solvents. Its pharmacology is similar to the stimulant desoxypipradrol in which the pyridine ring is reduced to a piperidine and for which it is a chemical precursor.
Hydromelonic acid, is an elusive chemical compound with formula C
9H
3N
13 or (HNCN)
3(C
6N
7), whose molecule would consist of a heptazine H3(C
6N
7) molecule, with three cyanamido groups H–N=C=N– or N≡C–NH– substituted for the hydrogen atoms.
Cobalt compounds are chemical compounds formed by cobalt with other elements.
A selenocyanate is an ion or chemical compound that contains the -SeCN group, which could be in the form of an anion, SeCN−. Organic selenocyanates also exist.
Transition metal complexes of thiocyanate describes coordination complexes containing one or more thiocyanate (SCN-) ligands. The topic also includes transition metal complexes of isothiocyanate. These complexes have few applications but played significant role in the development of coordination chemistry.