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  2. Thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Thiocyanate

    Thiocyanate [6] is known to be an important part in the biosynthesis of hypothiocyanite by a lactoperoxidase. [7] [8] [9] Thus the complete absence of thiocyanate or reduced thiocyanate [10] in the human body, (e.g., cystic fibrosis) is damaging to the human host defense system.

  3. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Lewis structure of a water molecule. Lewis structures – also called Lewis dot formulas, Lewis dot structures, electron dot structures, or Lewis electron dot structures (LEDs) – are diagrams that show the bonding between atoms of a molecule, as well as the lone pairs of electrons that may exist in the molecule.

  4. Thiocyanic acid - Wikipedia

    en.wikipedia.org/wiki/Thiocyanic_acid

    The esters of thiocyanic acid have the general structure R−S−C≡N, where R stands for an organyl group. Isothiocyanic acid, HNCS, is a Lewis acid whose free energy, enthalpy and entropy changes for its 1:1 association with a variety of Lewis bases in carbon tetrachloride solution at 25 °C have been reported.

  5. Transition metal complexes of thiocyanate - Wikipedia

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

    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.

  6. Thiocyanogen - Wikipedia

    en.wikipedia.org/wiki/Thiocyanogen

    3(SCN) 2 + 4H 2 O → H 2 SO 4 + HCN + 5HSCN. Thiocyanogen is a weak electrophile, attacking only highly activated (phenolic or anilinic) or polycyclic arenes. [1]: 243–245 It attacks carbonyls at the α position. [1] Heteratoms are attacked more easily, and the compound thiocyanates sulfur, nitrogen, and various poor metals.

  7. Sulfur dicyanide - Wikipedia

    en.wikipedia.org/wiki/Sulfur_dicyanide

    [2]: 8 It is the first member of the dicyanosulfanes S x (CN) 2, which includes thiocyanogen ((SCN) 2) and higher polysulfanes up to S 4 (CN) 2. [3] According to X-ray crystallography, the molecule is planar, the SCN units are linear, with an S-C-S angle of 95.6°. [4] Sulfur dicyanide begins to sublime at 30-40 °C and melts at 60 °C. [5]

  8. Scandium compounds - Wikipedia

    en.wikipedia.org/wiki/Scandium_compounds

    The halides are Lewis acids; for example, ScF 3 dissolves in a solution containing excess fluoride ion to form [ScF 6] 3−. The coordination number 6 is typical for Sc(III). In the larger Y 3+ and La 3+ ions, coordination numbers of 8 and 9 are common. Scandium triflate is sometimes used as a Lewis acid catalyst in organic chemistry.

  9. Sodium thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Sodium_thiocyanate

    Sodium thiocyanate (sometimes called sodium sulphocyanide) is the chemical compound with the formula NaSCN. This colorless deliquescent salt is one of the main sources of the thiocyanate anion.