Sulfur compounds

Short description: Chemical compounds with a sulfur atom

Sulfur compounds are chemical compounds formed the element sulfur (S). Common oxidation states of sulfur range from −2 to +6. Sulfur forms stable compounds with all elements except the noble gases.

Electron transfer reactions

Lapis lazuli owes its blue color to a trisulfur radical anion (S−3)

Sulfur polycations, S₈²⁺, S₄²⁺ and S₁₆²⁺ are produced when sulfur is reacted with oxidising agents in a strongly acidic solution.^[1] The colored solutions produced by dissolving sulfur in oleum were first reported as early as 1804 by C.F. Bucholz, but the cause of the color and the structure of the polycations involved was only determined in the late 1960s. S₈²⁺ is deep blue, S₄²⁺ is yellow and S₁₆²⁺ is red.^[2]

Reduction of sulfur gives various polysulfides with the formula S_x^2-, many of which have been obtained crystalline form. Illustrative is the production of sodium tetrasulfide:

4 Na + S
8 → 2 Na
2S
4

Some of these dianions dissociate to give radical anions, such as S₃⁻ gives the blue color of the rock lapis lazuli.

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]

This reaction highlights a distinctive property of sulfur: its ability to catenate (bind to itself by formation of chains). Protonation of these polysulfide anions produces the polysulfanes, H₂S_x where x= 2, 3, and 4.^[4] Ultimately, reduction of sulfur produces sulfide salts:

16 Na + S₈ → 8 Na₂S

The interconversion of these species is exploited in the sodium–sulfur battery.

Hydrogen sulfide

Treatment of sulfur with hydrogen gives hydrogen sulfide. When dissolved in water, hydrogen sulfide is mildly acidic:^[5]

H₂S ⇌ 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.

Oxides

The two principal sulfur oxides are obtained by burning sulfur:

S + O₂ → SO₂ (sulfur dioxide)

2 SO₂ + O₂ → 2 SO₃ (sulfur trioxide)

Many other sulfur oxides are observed including the sulfur-rich oxides include sulfur monoxide, disulfur monoxide, disulfur dioxides, and higher oxides containing peroxo groups.

Halides

Sulfur reacts with fluorine to give the highly reactive sulfur tetrafluoride and the highly inert Sulfur hexafluoride.^[6] Whereas fluorine gives S(IV) and S(VI) compounds, chlorine gives S(II) and S(I) derivatives. Thus, sulfur dichloride, disulfur dichloride, and higher chlorosulfanes arise from the chlorination of sulfur. Sulfuryl chloride and chlorosulfuric acid are derivatives of sulfuric acid; thionyl chloride (SOCl₂) is a common reagent in organic synthesis.^[7]

Pseudohalides

Sulfur oxidizes cyanide and sulfite to give thiocyanate and thiosulfate, respectively.

Metal sulfides

Sulfur reacts with many metals. Electropositive metals give polysulfide salts. Copper, zinc and silver are tarnished by slfur. Although many metal sulfides are known, most are prepared by high temperature reactions of the elements.^[8] Sulfide minerals contain the sulfide (S^2-) or disulfide (S₂^2-) anions. Typical examples are:

Acanthite Ag
2S
Chalcocite Cu
2S
Galena PbS
Sphalerite ZnS
Chalcopyrite CuFeS
2
Millerite NiS
Cinnabar HgS
Stibnite Sb
2S
3
Pyrite FeS
2
Molybdenite MoS
2

Organic compounds

Main page: Chemistry:Organosulfur compounds

Illustrative organosulfur compounds
Allicin, a chemical compound in garlic
(R)-cysteine, an amino acid containing a thiol group
Methionine, an amino acid containing a thioether
Diphenyl disulfide, a representative disulfide
Perfluorooctanesulfonic acid, a surfactant
Dibenzothiophene, a component of crude oil
Penicillin, an antibiotic where "R" is the variable group

Some of the main classes of sulfur-containing organic compounds include the following:^[9]

Thiols or mercaptans (so called because they capture mercury as chelators) are the sulfur analogs of alcohols; treatment of thiols with base gives thiolate ions.
Thioethers are the sulfur analogs of ethers.
Sulfonium ions have three groups attached to a cationic sulfur center. Dimethylsulfoniopropionate (DMSP) is one such compound, important in the marine organic sulfur cycle.
Sulfoxides and sulfones are thioethers with one and two oxygen atoms attached to the sulfur atom, respectively. The simplest sulfoxide, dimethyl sulfoxide, is a common solvent; a common sulfone is sulfolane.
Sulfonic acids are used in many detergents.

Compounds with carbon–sulfur multiple bonds are uncommon, an exception being carbon disulfide, a volatile colorless liquid that is structurally similar to carbon dioxide. It is used as a reagent to make the polymer rayon and many organosulfur compounds. Unlike carbon monoxide, carbon monosulfide is stable only as an extremely dilute gas, found between solar systems.^[10]

Organosulfur compounds are responsible for some of the unpleasant odors of decaying organic matter. They are widely known as the odorant in domestic natural gas, garlic odor, and skunk spray. Not all organic sulfur compounds smell unpleasant at all concentrations: the sulfur-containing monoterpenoid (grapefruit mercaptan) in small concentrations is the characteristic scent of grapefruit, but has a generic thiol odor at larger concentrations. Sulfur mustard, a potent vesicant, was used in World War I as a disabling agent.^[11]

Sulfur–sulfur bonds are a structural component used to stiffen rubber, similar to the disulfide bridges that rigidify proteins (see biological below). In the most common type of industrial "curing" or hardening and strengthening of natural rubber, elemental sulfur is heated with the rubber to the point that chemical reactions form disulfide bridges between isoprene units of the polymer. 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.

References

↑ Shriver, Atkins. Inorganic Chemistry, Fifth Edition. W. H. Freeman and Company, New York, 2010; pp 416
↑ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. pp. 645–665. ISBN 978-0-08-037941-8.
↑ Fujimori, Toshihiko; Morelos-Gómez, Aarón; Zhu, Zhen; Muramatsu, Hiroyuki; Futamura, Ryusuke; Urita, Koki; Terrones, Mauricio; Hayashi, Takuya et al. (2013). "Conducting linear chains of sulphur inside carbon nanotubes". Nature Communications 4: 2162. doi:10.1038/ncomms3162. PMID 23851903. Bibcode: 2013NatCo...4.2162F.
↑ Handbook of Preparative Inorganic Chemistry, 2nd ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 421.
↑ Greenwood, N. N.; & Earnshaw, A. (1997). Chemistry of the Elements (2nd ed.), Oxford:Butterworth-Heinemann. ISBN:0-7506-3365-4.
↑ Hasek, W. R. (1961). "1,1,1-Trifluoroheptane". Organic Syntheses 41: 104. doi:10.1002/0471264180.os041.28.
↑ Rutenberg, M. W.; Horning, E. C. (1950). "1-Methyl-3-ethyloxindole". Organic Syntheses 30: 62. doi:10.15227/orgsyn.030.0062.
↑ Vaughan, David J.; Craig, James R. (1978). Mineral chemistry of metal sulfides. Cambridge earth science series. Cambridge London New york [etc.]: Cambridge university press. ISBN 978-0-521-21489-6.
↑ Cremlyn R. J. (1996). An Introduction to Organosulfur Chemistry. Chichester: John Wiley and Sons. ISBN 0-471-95512-4.
↑ Wilson, R. W.; Penzias, A. A.; Wannier, P. G.; Linke, R. A. (15 March 1976). "Isotopic abundances in interstellar carbon monosulfide". Astrophysical Journal 204: L135–L137. doi:10.1086/182072. Bibcode: 1976ApJ...204L.135W.
↑ Banoub, Joseph (2011). Detection of Biological Agents for the Prevention of Bioterrorism. NATO Science for Peace and Security Series A: Chemistry and Biology. p. 183. doi:10.1007/978-90-481-9815-3. ISBN 978-90-481-9815-3. OCLC 697506461. Bibcode: 2011dbap.book.....B.

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[1] Shriver, Atkins. Inorganic Chemistry, Fifth Edition. W. H. Freeman and Company, New York, 2010; pp 416

[Greenwood-2] Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. pp. 645–665. ISBN 978-0-08-037941-8.

[3] Fujimori, Toshihiko; Morelos-Gómez, Aarón; Zhu, Zhen; Muramatsu, Hiroyuki; Futamura, Ryusuke; Urita, Koki; Terrones, Mauricio; Hayashi, Takuya et al. (2013). "Conducting linear chains of sulphur inside carbon nanotubes". Nature Communications 4: 2162. doi:10.1038/ncomms3162. PMID 23851903. Bibcode: 2013NatCo...4.2162F.

[4] Handbook of Preparative Inorganic Chemistry, 2nd ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 421.

[Greenwd-5] Greenwood, N. N.; & Earnshaw, A. (1997). Chemistry of the Elements (2nd ed.), Oxford:Butterworth-Heinemann. ISBN:0-7506-3365-4.

[6] Hasek, W. R. (1961). "1,1,1-Trifluoroheptane". Organic Syntheses 41: 104. doi:10.1002/0471264180.os041.28.

[7] Rutenberg, M. W.; Horning, E. C. (1950). "1-Methyl-3-ethyloxindole". Organic Syntheses 30: 62. doi:10.15227/orgsyn.030.0062.

[8] Vaughan, David J.; Craig, James R. (1978). Mineral chemistry of metal sulfides. Cambridge earth science series. Cambridge London New york [etc.]: Cambridge university press. ISBN 978-0-521-21489-6.

[Cremlyn-9] Cremlyn R. J. (1996). An Introduction to Organosulfur Chemistry. Chichester: John Wiley and Sons. ISBN 0-471-95512-4.

[10] Wilson, R. W.; Penzias, A. A.; Wannier, P. G.; Linke, R. A. (15 March 1976). "Isotopic abundances in interstellar carbon monosulfide". Astrophysical Journal 204: L135–L137. doi:10.1086/182072. Bibcode: 1976ApJ...204L.135W.

[11] Banoub, Joseph (2011). Detection of Biological Agents for the Prevention of Bioterrorism. NATO Science for Peace and Security Series A: Chemistry and Biology. p. 183. doi:10.1007/978-90-481-9815-3. ISBN 978-90-481-9815-3. OCLC 697506461. Bibcode: 2011dbap.book.....B.

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