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Although the biological oxidation of reduced sulfur compounds competes with abiotic chemical reactions (e.g. the iron-mediated oxidation of sulfide to iron sulfide (FeS) or pyrite (FeS 2)), [10] thermodynamic and kinetic considerations suggest that biological oxidation far exceeds the chemical oxidation of sulfide in most environments. [4]
Dibenzyl sulfide is a symmetrical thioether. It contains two C 6 H 5 CH 2 - (benzyl) groups linked by a sulfide bridge. It is a colorless or white solid that is soluble in nonpolar solvents.
The bacterial oxidation process comprises contacting refractory sulfide ROM ore or concentrate with a strain of the bacterial culture for a suitable treatment period under an optimum operating environment. The bacteria oxidise the sulfide minerals, thus liberating the occluded gold for subsequent recovery via cyanidation.
The assembly of iron–sulfur clusters cluster begins with the production of the equivalent of a sulfur (sulfur atoms per se are not found in nature). The required sulfur atom is obtained from free cysteine by the action of so-called cysteine desulfurases. One prominent desulfurase is called IscS, a pyridoxal phosphate-dependent enzyme.
Fractional oxidation states are often used to represent the average oxidation state of several atoms of the same element in a structure. For example, the formula of magnetite is Fe 3 O 4, implying an average oxidation state for iron of + 8 / 3 . [17]: 81–82 However, this average value may not be representative if the atoms are not ...
Sulfur can be found under several oxidation states in nature, mainly −2, −1, 0, +2 (apparent), +2.5 (apparent), +4, and +6. When two sulfur atoms are present in the same polyatomic oxyanion in an asymmetrical situation, i.e, each bound to different groups as in thiosulfate, the oxidation state calculated from the known oxidation state of accompanying atoms (H = +1, and O = −2) can be an ...
Iron shows the characteristic chemical properties of the transition metals, namely the ability to form variable oxidation states differing by steps of one and a very large coordination and organometallic chemistry: indeed, it was the discovery of an iron compound, ferrocene, that revolutionalized the latter field in the 1950s. [1]
Iron–sulfur clusters are molecular ensembles of iron and sulfide. They are most often discussed in the context of the biological role for iron–sulfur proteins , which are pervasive. [ 2 ] Many Fe–S clusters are known in the area of organometallic chemistry and as precursors to synthetic analogues of the biological clusters.