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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°.
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.
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°.
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.
In the yellow-coloured isomer, the nitro ligand is bound through nitrogen. In the red linkage isomer, the nitrito is bound through one oxygen atom. The O-bonded isomer is often written as [Co(NH 3) 5 (ONO)] 2+. Although the existence of the isomers had been known since the late 1800s, only in 1907 was the difference explained. [2]
Calcium thiocyanate refers to the salt Cs(SCN) 2. It is a colorless solid. According to X-ray crystallography, it is a coordination polymer. The Ca 2+ ions are each bonded to eight thiocyanate anions, with four Ca-S and four Ca-N bonds. The motif is reminiscent of the fluorite structure. [1]
New details about a study that warned against black plastic spatulas and other kitchen tools have come out. (Getty Creative) (Анатолий Тушенцов via Getty Images)
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