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The term sulfide (also spelled sulphide, see spelling) refers to several types of chemical compounds containing sulfur in its lowest oxidation number of −2.

Formally, "sulfide" is the dianion, S2−, which exists in strongly alkaline aqueous solutions formed from H2S or alkali metal salts such as Li2S, Na2S, and K2S. Sulfide is exceptionally basic and, with a pKa > 14, it does not exist in appreciable concentrations even in highly alkaline water, being undetectable at pH < ~15 (8 M NaOH). Instead, sulfide combines with protons to form HS, which is variously called hydrogen sulfide ion, hydrosulfide ion, sulfhydryl ion, or bisulfide ion. At still lower pH's (<7), HS converts to H2S, hydrogen sulfide. Thus, the exact sulfur species obtained upon dissolving sulfide salts depends on the pH of the final solution.

Aqueous solutions of transition metal cations react with sulfide sources (H2S, NaSH, Na2S) to precipitate solid sulfides. Such inorganic sulfides typically have very low solubility in water and many are related to minerals. One famous example is the bright yellow species CdS or "cadmium yellow". The black tarnish formed on sterling silver is Ag2S. Such species are sometimes referred to as salts. In fact the bonding in transition metal sulfides is highly covalent, which gives rise to their semiconductor properties, which in turn is related to the practical applications of many sulfide materials.

In organic chemistry, "sulfide" usually refers to the linkage C-S-C, although the term thioether is less ambiguous. For example, the thioether dimethyl sulfide is CH3-S-CH3. Polyphenylene sulfide (see below) has the empirical formula C6H4S. Occasionally, the term sulfide refers to molecules containing the -SH functional group. For example, methyl suflide can mean CH3-SH. The preferred descriptor for such SH-containing compounds is thiol or mercaptan, i.e. methanethiol or methyl mercaptan.

Confusion arises from the different meanings of the term "disulfide". Molybdenum disulfide consists of separated sulfide centers, in association with molybdenum in the formal 4+ oxidation state. Iron disulfide on the other hand consists of S22−, or S-S, in association with iron in the formal 2+ oxidation state. Dimethyldisulfide has the connectivity CH3-S-S-CH3, whereas carbon disulfide has no S-S linkages, being S=C=S.



Natural occurrence

Many important metal ores are sulfides. Significant sulfide minerals include:


Many metal sulfides are so insoluble that they are probably not very toxic. Some metal sulfides, when exposed to a strong mineral acid, including gastric acids, will release toxic hydrogen sulfide.

Organic sulfides are highly flammable. When a sulfide burns, the fumes usually include toxic sulfur dioxide (SO2) gas.

Hydrogen sulfide, some of its salts, and almost all organic sulfides have a strong and putrid stench, as rotting biomass releases these. Mercaptans, in particular, are the strongest-smelling substances known.


  • Meyer B, Ward K, Koshlap K, Peter L (1983). Second dissociation constant of hydrogen sulfide. Inorg Chem, 22:2345.

See also

bg:Сулфид ca:Sulfur da:Sulfid de:Sulfide et:Sulfiidid eo:Sulfido it:Solfuri nl:Sulfide no:Sulfid sr:Сулфид fi:Sulfidi sv:Sulfider