Chemistry:Phosphorus sulfides
Phosphorus sulfides comprise a family of inorganic compounds containing only phosphorus and sulfur. These compounds have the formula P
4S
n with n ≤ 10. Two are of commercial significance, phosphorus pentasulfide (P
4S
10), which is made on a kiloton scale for the production of other organosulfur compounds, and phosphorus sesquisulfide (P
4S
3), used in the production of "strike anywhere matches".
There are several other phosphorus sulfides in addition to P
4S
3 and P
4S
10. Six of these phosphorus sulfides exist as isomers: P
4S
4, P
4S
5, P
4S
6, P
4S
7, P
4S
8, and P
4S
9. These isomers are distinguished by Greek letter prefixes. The prefix is based on the order of the discovery of the isomers, not their structure.[1] All known molecular phosphorus sulfides contain a tetrahedral array of four phosphorus atoms.[2] P
4S
2 is also known but is unstable above −30 °C.[3]
Preparation
The main method for preparing these compounds is thermolysis of mixtures of phosphorus and sulfur. The product distributions can be analyzed by 31P-NMR spectroscopy. More selective syntheses entail:
- desulfurization, e.g. using triphenylphosphine and, complementarily,
- sulfidation using triphenylarsine sulfide.[4][5]
P
4S
3
Phosphorus sesquisulfide is prepared by treating red phosphorus with sulfur above 450 K,[6] followed by careful recrystallization with carbon disulfide and benzene. An alternative method involves the controlled fusion of white phosphorus with sulfur in an inert, non-flammable solvent.[7]
P
4S
4
The α- and β- forms of P
4S
4 can be prepared by treating the corresponding isomers of P
4S
3I
2 with ((CH
3)
3Sn)
2S:[6]
P
4S
3I
2 can be synthesized by the reaction of stoichiometric amounts of phosphorus, sulfur, and iodine.
P
4S
5
P
4S
5 can be prepared by treating stoichiometric amounts of P
4S
3 with sulfur in carbon disulfide solution, in the presence of light and a catalytic amount of iodine.[8] The respective product distribution is then analyzed by using 31P-NMR spectroscopy.
In particular, α-P
4S
5 can be easily made by the photochemical reaction of P
4S
10 with red phosphorus.[6] Note that P
4S
5 is unstable when heated, tending to disproportionate to P
4S
3 and P
4S
7 before reaching its melting point.[9]
P
4S
6
P
4S
6 can be made by abstracting a sulfur atom from P
4S
7 using triphenylphosphine:[6]
- P
4S
7 + Ph
3P → P
4S
6 + Ph
3PS
Treating α-P
4S
5 with Ph
3AsS in CS
2 also yields α-P
4S
6.[4] The two new polymorphs δ-P
4S
6 and ε-P
4S
6 can be made by treating α-P
4S
4 with Ph
3SbS in CS
2.[10]
P
4S
7
P
4S
7 is most conveniently made by direct union of the corresponding elements, and is one of the most easily purified binary phosphorus sulfides.[11]
- P
4 + 7 S → P
4S
7
P
4S
8
β-P
4S
8 can be made by treating α-P
4S
7 with Ph
3AsS in CS
2, which yields a mixture between α-P
4S
7 and β-P
4S
8.[4]
P
4S
9
P
4S
9 can be made by two methods. One method involves the heating of P
4S
3 in excess sulfur.[6] Another
method involves the heating of P
4S
7 and P
4S
10 in 1:2 mole ratio, where P
4S
9 is reversibly formed:[10]
- P
4S
7 + 2 P
4S
10 ⇌ 3 P
4S
9
P
4S
10
P
4S
10 is one of the most stable phosphorus sulfides. It is most easily made by heating white phosphorus with sulfur above 570 K in an evacuated tube.[12]
- P
4 + 10 S → P
4S
10
See also
- Diphosphorus trisulfide (P
2S
3)
References
- ↑ Jason, M. E.; Ngo, T.; Rahman, S. (1997). "Products and Mechanisms in the Oxidation of Phosphorus by Sulfur at Low Temperature". Inorg. Chem. 36 (12): 2633–2640. doi:10.1021/ic9614879.
- ↑ Holleman, A. F.; Wiberg, E. Inorganic Chemistry. Academic Press: San Diego, 2001. ISBN:0-12-352651-5.
- ↑ Heal, H. G. The Inorganic Heterocyclic Chemistry of Sulfur, Nitrogen, and Phosphorus Academic Press: London; 1980 ISBN:0-12-335680-6.
- ↑ 4.0 4.1 4.2 Jason, M. E. (1997). "Transfer of Sulfur from Arsenic and Antimony Sulfides to Phosphorus Sulfides. Rational Syntheses of Several Less-Common P4Sn Species". Inorg. Chem. 36 (12): 2641–2646. doi:10.1021/ic9614881.
- ↑ Nowottnick, H.; Blachnik, R. (1999). "Zwei neue Phosphorsulfide (Two New Phosphorus Sulfides)". Zeitschrift für anorganische und allgemeine Chemie 625 (12): 1966–1968. doi:10.1002/(SICI)1521-3749(199912)625:12<1966::AID-ZAAC1966>3.0.CO;2-B.
- ↑ 6.0 6.1 6.2 6.3 6.4 Catherine E. Housecroft; Alan G. Sharpe (2008). "Chapter 15: The group 15 elements". Inorganic Chemistry, 3rd Edition. Pearson. p. 484. ISBN 978-0-13-175553-6.
- ↑ "Phosphorus trisulfide" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 563.
- ↑ "Phosphorus pentasulfide" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 565.
- ↑ A. Earnshaw; Norman Greenwood (2002). "Phosphorus". Chemistry of the elements, 2nd edition. Butterworth Heinemann. p. 508. ISBN 0750633654.
- ↑ 10.0 10.1 R. Bruce King (2005). "Phosphorus". Encyclopedia of Inorganic Chemistry, 2nd edition. Wiley. p. 3711. ISBN 9780470862100.
- ↑ "Phosphorus heptasulfide" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 566.
- ↑ "Diphosphorus pentasulfide" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 567.
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