|Phosphorus trichloridePhosphorus trichloride|
|Systematic name||Phosphorus trichloride|
|Other names||Phosphorus(III) chloride|
|Molar mass||137.33 g/mol|
Diethyl ether: soluble
|Melting point||-93.6 °C (179.6 K)|
|Boiling point||76.1 °C (349.3 K)|
of formation ΔfH0liq
|−319.7 kJ/ mol (liquid)|
|Molecular geometry||Trigonal pyramidal|
|Bond angle||100 °|
|Bond length||P-Cl 204 pm (2.04 Å)|
|Dipole moment||0.56 D|
|Main hazards||Corrosive, toxic|
|R/S statement||R: 14-26/28-29-35-48/20 |
|Supplementary data page|
|nD = 1.4080 (25 C)|
Solid, liquid, gas
|Spectral data||UV, IR, NMR, MS|
|Except where noted otherwise, data are given for|
materials in their standard state (at 25°C, 100 kPa)
Infobox disclaimer and references
Phosphorus trichloride (formula PCl3) is the most important of the three phosphorus chlorides. It is an important industrial chemical, being used for the manufacture of organophosphorus compounds for a wide variety of applications.
The phosphorus in PCl3 is often considered to have the +3 oxidation state and the chlorine atoms are considered to be in the -1 oxidation state. Most of its reactivity is consistent with this description.
PCl3 as an electrophile
Phosphorus trichloride is the precursor to organophosphorus compounds that contain one or more (P3+) atoms, most notably phosphites and phosphonates. These compounds do not usually contain the chlorine atoms found in PCl3.
PCl3 reacts rapidly and exothermically with water to form phosphorous acid, H3PO3 and HCl. A large number of similar substitution reactions are known, the most important of which is the formation of phosphite esters by reaction with alcohols or phenols. For example, with phenol, triphenyl phosphite is formed:
where "Ph" stands for phenyl group, -C6H5. Alcohols such as ethanol react similarly in the presence of a base such as triethylamine to give phosphite esters such as triethyl phosphite (ethyl is -C2H5):
- 3 C2H5OH + PCl3 → P(OC2H5)3 + 3 HCl
- PCl3 + 3 C2H5OH → (C2H5O)2P(=O)H + C2H5Cl + 2 HCl
- R2NH + PCl3 + CH2O → (HO)2P(O)CH2NR2 + 3 HCl
Aminophosphonates are widely used as sequestring and antiscale agents in water treatment. The large volume herbicide glyphosate is also produced this way. The reaction of PCl3 with Grignard reagents and organolithium reagents is a useful method for the preparation of organic phosphines with the formula R3P (sometimes called phosphanes) such as triphenylphosphine, Ph3P.
- 3 PhMgBr + PCl3 → Ph3P + 3 MgBrCl
Under controlled conditions PCl3 can be used to prepare PhPCl2 and Ph2PCl.
PCl3 as a nucleophile
Phosphorus trichloride has a lone pair, and therefore can act as a Lewis base, for example with the Lewis acids BBr3 it forms a 1:1 adduct, Br3B−−+PCl3. Metal complexes such as Ni(PCl3)4 are known. This Lewis basicity is exploited in one useful route to organophosphorus compounds:
The (RPCl3)+ product can then be decomposed with water to produce an alkylphosphonic dichloride RP(=O)Cl2.
World production exceeds one-third of a million tonnes. Phosphorus trichloride is prepared industrially by the reaction of chlorine with a refluxing solution of white phosphorus in phosphorus trichloride, with continuous removal of PCl3 as it is formed.
Industrial production of phosphorus trichloride is controlled under the Chemical Weapons Convention, where it is listed in schedule 3.In the laboratory it may be more convenient to use the less toxic red phosphorus. It is sufficiently inexpensive that it would not be synthesized for laboratory use.
For example oxidation of PCl3 gives POCl3, which is used for the manufacture of triphenyl phosphate and tricresyl phosphate, which find application as flame retardants and plasticisers for PVC. They are also used to make insecticides such as diazinon. Phosphonates include the herbicide glyphosate.
PCl3 is the precursor to triphenylphosphine for the Wittig reaction, and phosphite esters which may be used as industrial intermediates, or used in the Horner-Wadsworth-Emmons reaction, both important methods for making alkenes. It can be used to make trioctylphosphine oxide (TOPO), used as an extraction agent, although TOPO is usually made via the corresponding phosphine.
PCl3 is also used directly as a reagent in organic synthesis. It is used to convert primary and secondary alcohols into alkyl chlorides, or carboxylic acids into acyl chlorides, although thionyl chloride generally gives better yields than PCl3.
PCl3 is toxic, with a concentration of 600 ppm being lethal in just a few minutes. PCl3 is classified as very toxic and corrosive under EU Directive 67/548/EEC, and the risk phrases R14, R26/28, R35 and R48/20 are obligatory.
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- N. N. Greenwood, A. Earnshaw, Chemistry of the Elements, 2nd ed., Butterworth-Heinemann, Oxford, UK, 1997.
- Handbook of Chemistry and Physics, 71st edition, CRC Press, Ann Arbor, Michigan, 1990.
- J. March, Advanced Organic Chemistry, 4th ed., p. 723, Wiley, New York, 1992.
- The Merck Index, 7th edition, Merck & Co, Rahway, New Jersey, USA, 1960.
- R. R. Holmes, Journal of Inorganic and Nuclear Chemistry 12, 266-275 (1960).
- M. C. Forbes, C. A. Roswell, R. N. Maxson, Inorganic Syntheses, Vol. II, 145-7 (1946).
- A. D. F. Toy, The Chemistry of Phosphorus, Pergamon Press, Oxford, UK, 1973.
- L. G. Wade, Jr., Organic Chemistry, 6th ed., p. 477, Pearson/Prentice Hall, Upper Saddle River, New Jersey, USA, 2005.