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  2. Organic thiocyanates - Wikipedia

    en.wikipedia.org/wiki/Organic_thiocyanates

    In methyl thiocyanate, N≡C and C−S distances are 116 and 176 pm. By contrast, N=C and C=S distances are 117 and 158 pm in isothiocyanates. [7] Typical bond angles for C−S−C are 100°. [3] By contrast C−N=C in aryl isothiocyanates is 165°. Again, the thiocyanate isomers are quite different with C−S−C angle near 100°.

  3. Isothiocyanate - Wikipedia

    en.wikipedia.org/wiki/Isothiocyanate

    By contrast, in methyl thiocyanate, N≡C and C−S distances are 116 and 176 pm. Typical bond angles for C−N=C in aryl isothiocyanates are near 165°. Again, the thiocyanate isomers are quite different with C−S−C angle near 100°. [3] In both isomers the SCN angle approaches 180°.

  4. Thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Thiocyanate

    [SCN] − is one of the pseudohalides, due to the similarity of its reactions to that of halide ions. Thiocyanate used to be known as rhodanide (from a Greek word for rose) because of the red colour of its complexes with iron. Thiocyanate is produced by the reaction of elemental sulfur or thiosulfate with cyanide: 8 CN − + S 8 → 8 SCN −

  5. Transition metal complexes of thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_complexes...

    Thiocyanate complexes are not widely used commercially. Possibly the oldest application of thiocyanate complexes was the use of thiocyanate as a test for ferric ions in aqueous solution. [15] The reverse was also used: testing for the presence of thiocyanate by the addition of ferric salts. The 1:1 complex of thiocyanate and iron is deeply red.

  6. Thiocyanic acid - Wikipedia

    en.wikipedia.org/wiki/Thiocyanic_acid

    One of the thiocyanic acid tautomers, HSCN, is predicted to have a triple bond between carbon and nitrogen. Thiocyanic acid has been observed spectroscopically. [12] The salts and esters of thiocyanic acid are known as thiocyanates. The salts are composed of the thiocyanate ion ([SCN] −) and a suitable cation (e.g., potassium thiocyanate, KSCN).

  7. Nickel(II) thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Nickel(II)_thiocyanate

    Nickel(II) thiocyanate is a coordination polymer with formula Ni(SCN) 2. [1] It is a green-brown solid and its crystal structure was determined first in 1982. [1]

  8. Mercury (II) thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Mercury(II)_thiocyanate

    Mercury(II) thiocyanate (Hg(SCN) 2) is an inorganic chemical compound, the coordination complex of Hg 2+ and the thiocyanate anion. It is a white powder. It is a white powder. It will produce a large, winding "snake" when ignited, an effect known as the Pharaoh's serpent .

  9. Copper(I) thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Copper(I)_thiocyanate

    Copper(I) thiocyanate is a hole conductor, a semiconductor with a wide band gap (3.6 eV, therefore transparent to visible and near infrared light). [11] It is used in photovoltaics in some third-generation cells as a hole transfer layer.