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Thiosulfate (IUPAC-recommended spelling; sometimes thiosulphate in British English) is an oxyanion of sulfur with the chemical formula S 2 O 2− 3.Thiosulfate also refers to the compounds containing this anion, which are the salts of thiosulfuric acid, such as sodium thiosulfate Na 2 S 2 O 3 and ammonium thiosulfate (NH 4) 2 S 2 O 3.
Eventually, [these] thioesters could have served to usher in ATP through its ability to support the formation of bonds between phosphate groups. However, due to the high free energy change of thioester's hydrolysis and correspondingly their low equilibrium constants, it is unlikely that these compounds could have accumulated abiotically to any ...
In the solid state, the thiosulfate anion is tetrahedral in shape and is notionally derived by replacing one of the oxygen atoms by a sulfur atom in a sulfate anion. The S-S distance indicates a single bond, implying that the terminal sulfur holds a significant negative charge and the S-O interactions have more double-bond character.
A chemical reaction involving the replacement of oxygen to sulfur is called thionation or thiation. Thio- can be prefixed with di- and tri- in chemical nomenclature. The word derives from Ancient Greek θεῖον (theîon) 'sulfur' (which occurs in Greek epic poetry as θέ(ϝ)ειον , théweion and may come from the same root as Latin fumus ...
One problem with this alternative process is the high consumption of thiosulfate, which is more expensive than cyanide. Another issue is the lack of a suitable recovery technique since [Au(S 2 O 3 ) 2 ] 3− does not adsorb to activated carbon , which is the standard technique used in gold cyanidation to separate the gold complex from the ore ...
The S−H bond in thiols is weak compared to the O−H bond in alcohols. For CH 3 X−H, the bond enthalpies are 365.07 ± 2.1 kcal/mol for X = S and 440.2 ± 3.0 kcal/mol for X = O. [ 21 ] Hydrogen-atom abstraction from a thiol gives a thiyl radical with the formula RS • , where R = alkyl or aryl.
Each oxygen atom in its peroxide ion may have a full octet of 4 pairs of electrons. [6] Superoxides are a class of compounds that are very similar to peroxides, but with just one unpaired electron for each pair of oxygen atoms (O − 2). [6] These compounds form by oxidation of alkali metals with larger ionic radii (K, Rb, Cs).
Double bonds occur most commonly between two carbon atoms, for example in alkenes. Many double bonds exist between two different elements: for example, in a carbonyl group between a carbon atom and an oxygen atom. Other common double bonds are found in azo compounds (N=N), imines (C=N), and sulfoxides (S=O).