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The cyanate ion is an with the . It is a resonance of three forms: (61%) ↔ (30%) ↔ (4%).

Cyanate is the derived anion of , H−N=C=O, and its lesser cyanic acid (a.k.a. cyanol), H−O−C≡N.

Any salt containing the ion, such as , is called a cyanate.

The cyanate ion is an of the much-less-stable anion, or .William R. Martin and David W. Ball (2019): "Small organic fulminates as high-energy materials. Fulminates of acetylene, ethylene, and allene". Journal of Energetic Materials, volume 31, issue 7, pages 70-79.

The cyanate ion is an ambidentate ligand, forming complexes with a metal ion in which either the nitrogen or oxygen atom may be the . It can also act as a .

Compounds that contain the cyanate , −O−C≡N, are known as cyanates or . The cyanate functional group is distinct from the functional group, −N=C=O; the functional group, ; and the functional group, or .


Cyanate ion
The three atoms in a cyanate ion lie on a straight line, giving the ion a linear structure. The electronic structure is described most simply as
:Ö̤−C≡N:
with a single C−O bond and a triple C≡N bond. (Or more completely as :Ö̤−C≡N: ↔ Ö̤=C=N̤̈ ↔ :O≡C−N̤̈:) The infrared spectrum of a cyanate salt has a band at ca. 2096 cm−1; such a high frequency is characteristic of a .Nakamoto, Part A, p171

The cyanate ion is a . Both the oxygen and nitrogen atoms carry a of electrons and either one, the other, or both can be donated to acceptors. It can be described as an ambidentate ligand.


Cyanate salts
is with sodium , confirming the linear structure of the cyanate ion.Wells, p722. It is made industrially by heating a mixture of and .Greenwood, p324
A similar reaction is used to make potassium cyanate. Cyanates are produced when are oxidized. Use of this fact is made in cyanide decontamination processes where oxidants such as and hydrogen peroxide are used to convert toxic cyanide into less-toxic cyanate.

NH4OCNtetragonalP4/nmma=5.082 b=5.082 c=5.551 decomposes when heated to
LiOCNtrigonalR ma = 3.230 b = 14.268 Z=3128.901.895melts at 475 °C
NaOCNhexagonalR ma = 3.568 c = 15.123166.721.94melts at 550 °C
Potassium cyanateKOCNtetragonalI4/ mcma = 6.091 c = 7.052261.62.056melts at 315 °C
RbOCNtetragonalI4/ mcma = 6.35 c = 7.38297.582.85 T. C. Waddington "Lattice parameters and infrared spectra of some inorganic cyanates" J. Chem. Soc., 1959, 2499-2502.
CsOCNtetragonalI4 mcma = 6.519 c = 7.994339.683.42
TlOCNtetragonalI4 mcma = 6.23 c = 7.32284.35.76
AgOCNmonoclinicP21/ ma = 5.474 b = 6.378 c = 3.417 β = 90.931°119.294.173melts at 652 °C
Strontium cyanateSr(OCN)2orthorhombicFddda = 6.151 b = 11.268 c = 11.848 Z = 8821.12.78


Complexes with the cyanate ion
Cyanate is an ambidentate ligand which can donate the pair of electrons on the nitrogen atom or the oxygen atom, or both. Structurally the isomers can be distinguished by the geometry of the complex. In N-bonded cyanate complexes the M−NCO unit sometimes has a linear structure, but with O-bonded cyanate the M−O−C unit is bent. Thus, the silver cyanato complex, , has a linear structure as shown by X-ray crystallography. (click here) However, the crystal structure of shows zigzag chains of nitrogen atoms and silver atoms. There also exists a structure
   NCO
  /   \
Ni    Ni
  \   /
   OCN
     
in which the Ni-N-C group is bent.

Infrared spectroscopy has been used extensively to distinguish between isomers. Many complexes of metals are N-bonded. O-Bonding has been suggested for complexes of the type , M = Mo(III), Re(IV), and Re(V). The yellow complex and orange complex are linkage isomers and show differences in their infrared spectra which can be used for diagnosis.Nakamoto, Part B, pp 121–123.

The cyanate ion can bridge between two metal atoms by using both its donor atoms. For example, this structure is found in the compound . In this compound both the Ni−N−C unit and Ni−O−C unit are bent, even though in the first case donation is through the nitrogen atom.Greenwood, Table 8.9


Cyanate functional group
Compounds that contain the cyanate , −O−C≡N, are known as cyanates or . cyanates such are phenyl cyanate, can be formed by a reaction of with cyanogen chloride, ClCN, in the presence of a base.

that contain the isocyanate −N=C=O are known as . It is conventional in organic chemistry to write isocyanates with two double bonds, which accords with a simplistic valence bond theory of the bonding. In nucleophilic substitution reactions cyanate usually forms an isocyanate. Isocyanates are widely used in the manufacture of products and ; methyl isocyanate, used to make pesticides, was a major factor in the .


See also


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