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Hydrogen cyanide (formerly known as prussic acid) is a chemical compound with the formula HCN and structural formula H−C≡N.It is a highly toxic and flammable liquid that boils slightly above room temperature, at 25.6 °C (78.1 °F).
Since the initial detection, HCNH + has also been observed in TMC-1 [15] [16] as well as DR 21(OH) [15]. [17] The initial detection toward Sgr B2 has also been confirmed. [15] [18] All 3 of these sources are dense molecular clouds, and to date HCNH + has not been detected in diffuse interstellar material.
Among the most toxic cyanides are hydrogen cyanide (HCN), sodium cyanide (NaCN), potassium cyanide (KCN), and calcium cyanide (Ca(CN) 2). The cyanide anion is an inhibitor of the enzyme cytochrome c oxidase (also known as aa 3 ), the fourth complex of the electron transport chain found in the inner membrane of the mitochondria of eukaryotic cells.
Interference with hydrogen is one of the reason for the molecule's instability due to the energetically favorable dissociation back into hydrogen cyanide and acetylene. [ 2 ] Cyanopolyynes were first discovered in interstellar molecular clouds in 1971 using millimeter wave and microwave telescopes . [ 1 ]
Cyanogen is typically generated from cyanide compounds. One laboratory method entails thermal decomposition of mercuric cyanide: . 2 Hg(CN) 2 → (CN) 2 + Hg 2 (CN) 2 Or, one can combine solutions of copper(II) salts (such as copper(II) sulfate) with cyanides; an unstable copper(II) cyanide is formed which rapidly decomposes into copper(I) cyanide and cyanogen.
Hydrogen isocyanide (HNC) is a linear triatomic molecule with C ∞v point group symmetry.It is a zwitterion and an isomer of hydrogen cyanide (HCN). [2] Both HNC and HCN have large, similar dipole moments, with μ HNC = 3.05 Debye and μ HCN = 2.98 Debye respectively. [3]
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, [Ag(NCO) 2] −, has a linear structure as shown by X-ray crystallography. [13]
Subsequent binding of the alkene gives the intermediate M(H)(CN)L n (alkene), which then undergoes migratory insertion to give an alkylmetal cyanide. The cycle is completed by the reductive elimination of the nitrile. Lewis acids, such as triphenylboron (B(C 6 H 5) 3), induce reductive elimination of the nitrile product, increasing rates. [1]