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The thiosulfate ion is tetrahedral at the central S atom. The thiosulfate ion has C 3v symmetry. The external sulfur atom has a valence of 2 while the central sulfur atom has a valence of 6. The oxygen atoms have a valence of 2. The S-S distance of about 201 pm in sodium thiosulphate is appropriate for a single bond.
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.
Tetrathionate has also been found to serve as a terminal electron acceptor for Salmonella enterica serotype Typhimurium, whereas existing thiosulfate in the small intestines of mammals is oxidized by reactive oxygen species released by the immune system (mainly NADPH oxidase produced superoxide) to form tetrathionate. This aids in the growth of ...
The advantages of this approach are that (i) thiosulfate is far less toxic than cyanide and (ii) that ore types that are refractory to gold cyanidation (e.g. carbonaceous or Carlin-type ores) can be leached by thiosulfate. One problem with this alternative process is the high consumption of thiosulfate, which is more expensive than cyanide.
Sodium tetrathionate is formed by the oxidation of sodium thiosulfate (Na 2 S 2 O 3), e.g. by the action of iodine: [1] 2 Na 2 S 2 O 3 + I 2 → Na 2 S 4 O 6 + 2 NaI. The reaction is signaled by the decoloration of iodine. This reaction is the basis of iodometric titrations. Other methods include the coupling of sodium bisulfite with disulfur ...
Aqueous solutions of sodium dithionite were once used to produce 'Fieser's solution' for the removal of oxygen from a gas stream. [11] Pyrithione can be prepared in a two-step synthesis from 2-bromopyridine by oxidation to the N -oxide with a suitable peracid followed by substitution using sodium dithionite to introduce the thiol functional group .
For example, from the word ether, referring to an oxygen-containing compound having the general chemical structure R−O−R′, where R and R′ are organic functional groups and O is an oxygen atom, comes the word thioether, which refers to an analogous compound with the general structure R−S−R′, where S is a sulfur atom covalently ...
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 ...