Cobalt(II) cyanate

Last updated
Cobalt(II) cyanate
Identifiers
3D model (JSmol)
PubChem CID
  • isocyanate:InChI=1S/2CNO.Co/c2*2-1-3;/q2*-1;+2
    Key: JXDJYNWFLIUUIU-UHFFFAOYSA-N
  • C(#N)[O-].C(#N)[O-].[Co+2]
  • isocyanate:C(=[N-])=O.C(=[N-])=O.[Co+2]
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.

Contents

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.

History

Cobalt(II) cyanate was claimed to have been produced in 1952 by carefully heating pyridine cobalt(II) cyanate under vacuum. This has not been proven. [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]

Complexes

Tetracyanatocobaltate(II)

A solution of tetracyanatocobaltate(II) Cobalt cyanate complex.jpg
A solution of tetracyanatocobaltate(II)

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]

4 KOCN + Co(NO3)2 → K2[Co(NCO)4] + 2 KNO3

Tetracyanatocobaltate(II) salts with other counterions, such as cobaltcenium [Co(C5H5)]+ and EMIM are known. [2]

Other adducts

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]

Structure

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]

Related Research Articles

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.

<span class="mw-page-title-main">Metallocene</span>

A metallocene is a compound typically consisting of two cyclopentadienyl anions (C
5
H
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.

<span class="mw-page-title-main">Thiocyanate</span> Ion (S=C=N, charge –1)

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 PsPs 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.

<span class="mw-page-title-main">Cyanate</span> Anion with formula OCN and charge –1

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%).

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.

<span class="mw-page-title-main">Sodium hexanitritocobaltate(III)</span> Chemical compound

Sodium hexanitritocobaltate(III) is 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.

<span class="mw-page-title-main">Mercury(II) thiocyanate</span> Chemical compound

Mercury(II) thiocyanate (Hg(SCN)2) 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.

<span class="mw-page-title-main">Cobalt(II) nitrate</span> Chemical compound

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..

<span class="mw-page-title-main">Cobalt(II) thiocyanate</span> Chemical compound

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.

<span class="mw-page-title-main">Chloro(pyridine)cobaloxime</span> Chemical compound

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.

<span class="mw-page-title-main">Silver cyanate</span> Chemical compound

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.

<span class="mw-page-title-main">Diphenyl-2-pyridylmethane</span> Chemical compound

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.

<span class="mw-page-title-main">Phosphenium</span> Divalent cations of phosphorus

Phosphenium ions, not to be confused with phosphonium or phosphirenium, are divalent cations of phosphorus of the form [PR2]+. Phosphenium ions have long been proposed as reaction intermediates.

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

Hydromelonic acid, is an elusive chemical compound with formula C
9
H
3
N
13
or (HNCN)
3
(C
6
N
7
)
, whose molecule would consist of a heptazine H3(C
6
N
7
)
molecule, with three cyanamido groups H–N=C=N– or N≡C–NH– substituted for the hydrogen atoms.

<span class="mw-page-title-main">Transition metal pyridine complexes</span>

Transition metal pyridine complexes encompass many coordination complexes that contain pyridine as a ligand. Most examples are mixed-ligand complexes. Many variants of pyridine are also known to coordinate to metal ions, such as the methylpyridines, quinolines, and more complex rings.

A nitrate nitrite, or nitrite nitrate, is a coordination complex or other chemical compound that contains both nitrite and nitrate anions (NO3 and NO2). They are mixed-anion compounds, and they are mixed-valence compounds. Some have third anions. Many nitrite nitrate compounds are coordination complexes of cobalt. Such a substance was discovered by Wolcott Gibbs and Frederick Genth in 1857.

Cobalt compounds are chemical compounds formed by cobalt with other elements.

References

  1. Albert V. Logan; David C. Bush; Charles J. Rogers (1952). "The Heats of Formation of Cobalt(II) and Nickel(II) Pyridinated Cyanates and Thiocyanates". Journal of the American Chemical Society. 74 (16): 4194–4195. doi:10.1021/ja01136a069.
  2. 1 2 3 4 Tim Peppel; Alexander Hinz; Philipp Thiele; Monika Geppert-Rybczyńska; Jochen K. Lehmann; Martin Köckerling (2017). "Synthesis, Properties, and Structures of Low-Melting Tetraisocyanatocobaltate(II)-Based Ionic Liquids". European Journal of Inorganic Chemistry (5): 885–893. doi:10.1002/ejic.201601250.
  3. C. W. Blomstrand (1871). "Zur Kenntniss der gepaarten Verbindungen des fünfatomigen Stickstoffs" [Towards the knowledge of the paired compounds of five-atom nitrogen]. Journal für Praktische Chemie (in German). 3 (1): 186–224. doi:10.1002/prac.18710030119.
  4. A.H. Norbury (1975). "Coordination Chemistry of the Cyanate, Thiocyanate, and Selenocyanate Ions". Advances in Inorganic Chemistry and Radiochemistry. 17: 231–386. doi:10.1016/S0065-2792(08)60064-3.
  5. Karin Ruhlandt-Senge; Irina Sens; Ulrich Müller (1991). "Die Bildung von [Co(C5H5)2]NO3 und [Co(C5H5)2]2[Co(NCO)4] aus Cobaltocen, Ozon und Acetonitril sowie deren Kristallstrukturen" [Formation of [Co(C5H5)2]NO3 and [Co(C5H5)2]2[Co(NCO)4] from Cobaltocene, Ozone and Acetonitrile and their Crystal Structures]. Zeitschrift für Naturforschung B (in German). 46 (12): 1689–1693. doi:10.1515/znb-1991-1218.
  6. F. Albert Cotton; Margaret Goodgame (1961). "Magnetic Investigations of Spin-free Cobaltous Complexes. V. Tetra-azido and Tetracyanato Cobaltate(II) Ions". Journal of the American Chemical Society. 83 (8): 1777–1780. doi:10.1021/ja01469a001.
  7. LI Jia; Ling-Qian Kong; Da-Cheng Li (2008). "cis-Bis-(2,2'-bipyrid-yl)dicyanato-cobalt(II)". Acta Crystallographica Section E. 64 (4): 582. doi:10.1107/S1600536808007617.
  8. A. B. P. Lever; S. M. Nelson (1966). "An analysis of the electronic spectra of bis-amine cobalt halides: a novel effect of steric hindrance". Journal of the Chemical Society A: Inorganic, Physical, Theoretical: 859–863. doi:10.1039/J19660000859.