Sulfur compounds

This reaction highlights a distinctive property of sulfur: its ability to catenate (bind to itself by formation of chains).

[4] Ultimately, reduction of sulfur produces sulfide salts: The interconversion of these species is exploited in the sodium–sulfur battery.

When dissolved in water, hydrogen sulfide is mildly acidic:[5] 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.

Typical examples are: Some of the main classes of sulfur-containing organic compounds include the following:[10] Compounds with carbon–sulfur multiple bonds are uncommon, an exception being carbon disulfide, a volatile colorless liquid that is structurally similar to carbon dioxide.

[12] Sulfur–sulfur bonds are a structural component used to stiffen rubber, similar to the disulfide bridges that rigidify proteins (see biological below).

This process, patented in 1843, made rubber a major industrial product, especially in automobile tires.

Because of the heat and sulfur, the process was named vulcanization, after the Roman god of the forge and volcanism.

Lapis lazuli owes its blue color to a trisulfur radical anion ( S
3
)
Two parallel sulfur chains grown inside a single-wall carbon nanotube (CNT, a). Zig-zag (b) and straight (c) S chains inside double-wall CNTs [ 3 ]