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  2. Microbial oxidation of sulfur - Wikipedia

    en.wikipedia.org/wiki/Microbial_oxidation_of_sulfur

    Reactions of oxidation of sulfide to sulfate and elemental sulfur (incorrectly balanced). The electrons (e −) liberated from these oxidation reactions, which release chemical energy, are then used to fix carbon into organic molecules. The elements that become oxidized are shown in pink, those that become reduced in blue, and the electrons in ...

  3. Sulfur - Wikipedia

    en.wikipedia.org/wiki/Sulfur

    Sulfur (also spelled sulphur in British English) is a chemical element; it has symbol S and atomic number 16. It is abundant, multivalent and nonmetallic. Under normal conditions, sulfur atoms form cyclic octatomic molecules with the chemical formula S 8. Elemental sulfur is a bright yellow, crystalline solid at room temperature.

  4. Organosulfur chemistry - Wikipedia

    en.wikipedia.org/wiki/Organosulfur_chemistry

    Nature is abound with organosulfur compounds—sulfur is vital for life. Of the 20 common amino acids, two (cysteine and methionine) are organosulfur compounds, and the antibiotics penicillin and sulfa drugs both contain sulfur. While sulfur-containing antibiotics save many lives, sulfur mustard is a deadly chemical warfare agent.

  5. Sulfur compounds - Wikipedia

    en.wikipedia.org/wiki/Sulfur_compounds

    Treatment of sulfur with hydrogen gives hydrogen sulfide.When dissolved in water, hydrogen sulfide is mildly acidic: [5] H 2 S ⇌ HS − + H +. Hydrogen sulfide gas and the hydrosulfide anion are extremely toxic to mammals, due to their inhibition of the oxygen-carrying capacity of hemoglobin and certain cytochromes in a manner analogous to cyanide and azide.

  6. Organic sulfide - Wikipedia

    en.wikipedia.org/wiki/Organic_sulfide

    This reaction is exploited in biological systems as a means of transferring an alkyl group. For example, S-adenosylmethionine acts as a methylating agent in biological S N 2 reactions. An unusual but well tested method for the synthesis of thioethers involves addition of alkenes, especially ethylene across the S-Cl bond of sulfur dichloride.

  7. 2,3-sigmatropic rearrangement - Wikipedia

    en.wikipedia.org/wiki/2,3-sigmatropic_rearrangement

    Atom Y may be sulfur, selenium, or nitrogen. If Y is nitrogen, the reaction is referred to as the Sommelet–Hauser rearrangement if a quaternary ammonium salt is involved or the aza-Wittig reaction if an alpha-metalated tertiary amine is involved; if Y is oxygen, then it is called a 2,3-Wittig rearrangement (not to be confused with the well ...

  8. Sulfation - Wikipedia

    en.wikipedia.org/wiki/Sulfation

    Sulfation is a process used to remove "sulfur" from the combustion of fossil fuels. The goal is to minimize the pollution by the combusted gases. Combustion of sulfur-containing fuels releases sulfur dioxide, which, in the atmosphere, oxidizes to the equivalent of sulfuric acid, which is corrosive.

  9. Sulfur metabolism - Wikipedia

    en.wikipedia.org/wiki/Sulfur_metabolism

    From the sulfide they form the amino acids cysteine and methionine, sulfolipids, and other sulfur compounds. Animals obtain sulfur from cysteine and methionine in the protein that they consume. Sulfur is the third most abundant mineral element in the body. [21] The amino acids cysteine and methionine are used by the body to make glutathione.

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