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Words near each other
・ Thiosulfate—dithiol sulfurtransferase
・ Thiosulfate—thiol sulfurtransferase
・ Thiosulfinate
・ Thiosulfoxide
・ Thiosulfuric acid
・ Thiosulfurous acid
・ Thiosymbescaline
・ Thiocarbohydrazide
・ Thiocarbonate
・ Thiocarbonic acid
・ Thiocarboxylic acid
・ Thiocarlide
・ Thiochroa
・ Thioclava
・ Thiocolchicoside
Thiocyanate
・ Thiocyanate hydrolase
・ Thiocyanate isomerase
・ Thiocyanatoiron
・ Thiocyanic acid
・ Thiocyanogen
・ Thiodia
・ Thiodia citrana
・ Thiodia glandulosana
・ Thiodia lerneana
・ Thiodia torridana
・ Thiodiglycol
・ Thiodina
・ Thiodiodes
・ Thioenol


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Thiocyanate : ウィキペディア英語版
Thiocyanate

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Thiocyanate (also known as rhodanide) is the anion (). It is the conjugate base of thiocyanic acid. Common derivatives include the colourless salts potassium thiocyanate and sodium thiocyanate. Organic compounds containing the functional group SCN are also called thiocyanates. Mercury(II) thiocyanate was formerly used in pyrotechnics.
Thiocyanate is analogous to the cyanate ion, (), wherein oxygen is replaced by sulfur. () 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 + S8 → 8 SCN
: CN + S2O32− → SCN + SO32−
The second reaction is catalyzed by the enzyme sulfotransferase known as rhodanase and may be relevant to detoxification of cyanide in the body.
==Organic thiocyanates==
Organic and transition metal derivatives of the thiocyanate ion can exist as "linkage isomers." In thiocyanates, the organic group (or metal ion) is attached to sulfur: R−S−C≡N has a S-C single bond and a C≡N triple bond. In isothiocyanates, the substituent is attached to nitrogen: R−N=C=S has a S=C double bond and a C=N double bond:

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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