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  2. Transition metal complexes of thiocyanate - Wikipedia

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

    Ru(PPh 3) 2 (CO) 3 + (SCN) 2 → Ru(NCS) 2 (PPh 3) 2 (CO) 2 + CO, where Ph = C 6 H 5. Even though the reaction involves cleavage of the S-S bond in thiocyanogen, the product is the Ru-NCS linkage isomer. In another unusual method, thiocyanate functions as both a ligand and as a reductant in its reaction with dichromate to give [Cr(NCS) 4 (NH 3 ...

  3. 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.

  4. Clar's rule - Wikipedia

    en.wikipedia.org/wiki/Clar's_rule

    Clar's rule states that for a benzenoid polycyclic aromatic hydrocarbon (i.e. one with only hexagonal rings), the resonance structure with the largest number of disjoint aromatic π-sextets is the most important to characterize its chemical and physical properties. Such a resonance structure is called a Clar structure. In other words, a ...

  5. Resonance (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Resonance_(chemistry)

    Contributing structures of the carbonate ion. In chemistry, resonance, also called mesomerism, is a way of describing bonding in certain molecules or polyatomic ions by the combination of several contributing structures (or forms, [1] also variously known as resonance structures or canonical structures) into a resonance hybrid (or hybrid structure) in valence bond theory.

  6. Organic thiocyanates - Wikipedia

    en.wikipedia.org/wiki/Organic_thiocyanates

    Sulfenyl thiosulfates (RSSO 3 −) react with alkali metal cyanides to give thiocyanates with displacement of sulfite. This approach has been applied to allyl thiocyanate: [6] CH 2 =CHCH 2 Cl + Na 2 S 2 O 3 → CH 2 =CHCH 2 S 2 O 3 Na + NaCl CH 2 =CHCH 2 S 2 O 3 Na + NaCN → CH 2 =CHCH 2 SCN + Na 2 SO 3. Sulfenyl chlorides (RSCl) also convert ...

  7. Thiocyanogen - Wikipedia

    en.wikipedia.org/wiki/Thiocyanogen

    Thiocyanogen, (SCN) 2, is a pseudohalogen derived from the pseudohalide thiocyanate, [SCN] −, with behavior intermediate between dibromine and diiodine. [2] This hexatomic compound exhibits C 2 point group symmetry and has the connectivity NCS-SCN. [3] In the lungs, lactoperoxidase may oxidize thiocyanate to thiocyanogen [4] or ...

  8. Mercury (II) thiocyanate - Wikipedia

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

    Because of this, a heptazine-based structure similar to Liebig's melon, a compound initially prepared around the same time that the pharoah's snake reaction was discovered, was not ruled out by the authors as a partial component of the solid material. [10] The generalized reaction is as follows: 2 Hg(SCN) 2 → 2 β−HgS + CS 2 + C 3 N 4

  9. Copper(II) thiocyanate - Wikipedia

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

    The structure of Cu(SCN) 2 was determined via powder X-ray diffraction and consists of chains of Cu(NCS) 2 linked together by weak Cu–S–Cu bonds into two-dimensional layers. It can be considered a Jahn–Teller distorted analogue of the mercury thiocyanate structure-type. Each copper is octahedrally coordinated by four sulfurs and two ...