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  2. Thiosulfate - Wikipedia

    en.wikipedia.org/wiki/Thiosulfate

    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.

  3. Sodium thiosulfate - Wikipedia

    en.wikipedia.org/wiki/Sodium_thiosulfate

    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.

  4. Tetrasulfur tetranitride - Wikipedia

    en.wikipedia.org/wiki/Tetrasulfur_tetranitride

    This compound, upon standing, isomerizes to additionally bond through a nitrogen atom. S 4 N 4 oxidatively adds to Vaska's complex ([Ir(Cl)(CO)(PPh 3) 2] to form a hexacoordinate iridium complex where the S 4 N 4 binds through two sulfur atoms and one nitrogen atom. [2] Dilute NaOH hydrolyzes S 4 N 4 as follows, yielding thiosulfate and ...

  5. Transition metal thiosulfate complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal...

    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.

  6. Nitrogen compounds - Wikipedia

    en.wikipedia.org/wiki/Nitrogen_compounds

    Its bonding is similar to that in nitrogen, but one extra electron is added to a π* antibonding orbital and thus the bond order has been reduced to approximately 2.5; hence dimerisation to O=N–N=O is unfavourable except below the boiling point (where the cis isomer is more stable) because it does not actually increase the total bond order ...

  7. Microbial oxidation of sulfur - Wikipedia

    en.wikipedia.org/wiki/Microbial_oxidation_of_sulfur

    The aforementioned Sox pathway, through which both sulfur atoms in thiosulfate are oxidized to sulfate without the formation of any free intermediate. [ 37 ] [ 38 ] [ 39 ] The oxidation of thiosulfate (S 2 O 3 2- ) via the formation of tetrathionate (S 4 O 6 2- ) intermediate, that is present in several obligate chemolithotrophic Gamma and ...

  8. Tetrathionate - Wikipedia

    en.wikipedia.org/wiki/Tetrathionate

    Two of the sulfur atoms present in the ion are in oxidation state 0 and two are in oxidation state +5. Alternatively, the compound can be viewed as the adduct resulting from the binding of S 2− 2 to SO 3. Tetrathionate is one of the polythionates, a family of anions with the formula [S n (SO 3) 2] 2−. [1]

  9. Thiosulfinate - Wikipedia

    en.wikipedia.org/wiki/Thiosulfinate

    Conversion of simple disulfides to thiosulfinates results in a considerable weakening of the S–S bond from about 47.8 to 28.0 kcal mol −1 for the S-S bond in PhS(O)SPh and from about 63.2 to 39.3 kcal mol −1 for the S-S bond in MeS(O)SMe, [14] with the consequence that most thiosulfinates are both unstable and quite reactive.