Thiophosphoryl fluoride

Thiophosphoryl fluoride  |

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Names
IUPAC name

Trifluoro(sulfanylidene)-λ5-phosphane

Other names

* Phosphorothioc trifluoride[1]
* Phosphorothioic trifluoride
* Phosphorus fluoride sulfide
* Phosphorus sulfurtrifluoride
* Phosphorus thiofluoride
* Thiophosphoryl trifluoride
* Trifluorophosphine sulfide
* Trifluoro-λ5-phosphanethione[2]

Identifiers

CAS Number

* 2404-52-6 N

3D model (JSmol)

* [3]: Interactive image

ChemSpider |

* 121246 N

PubChem CID

* 137585

InChI

* InChI=1S/F3PS/c1-4(2,3)5 N

Key: LHGOOQAICOQNRG-UHFFFAOYSA-N N

SMILES

* [3]: FP(F)(F)=S

Properties

Chemical formula

| PSF

Molar mass | 120.035 g/mol
Appearance  | Colorless gas or liquid
Density | 1.56g/cm3 liquid[4] 4.906 g/L as gas[1]
Melting point |  −148.8 °C (−235.8 °F; 124.3 K)
Boiling point |  −52.25 °C (−62.05 °F; 220.90 K)

Solubility in water

| slight, Highly reactive
Structure

Molecular shape

| Tetrahedral at the P atom
Hazards
Main hazards | Spontaneously flammable in air; toxic fumes
Flash point | very low
Related compounds

Related compounds

* Phosphoryl trifluoride
* Phosphorus trifluoride
* Thiazyl trifluoride
* Selenophosphoryl fluoride PSeF

* Thiophosphoryl chloride
* Phosphorothioc chloride difluoride

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Infobox references

Tracking categories (test):

* PairSizeSet

Thiophosphoryl fluoride is an inorganic molecular gas with formula PSF
3 containing phosphorus, sulfur and fluorine. It spontaneously ignites in air and burns with a cool flame. The discoverers were able to have flames around their hands without discomfort,[5] and called it "probably one of the coldest flames known".[5] The gas was discovered in 1888.[5]

It is useless for chemical warfare as it burns immediately and is not toxic enough.[6]

## Contents

* 1 Preparation
* 2 Reactions
* 2.1 Sulfur removal
* 2.2 Fluorine substitution
* 2.3 Cations
* 3 Related compounds
* 4 Physical properties
* 5 References
* 6 Other references

## Preparation

Thiophosphoryl fluoride was discovered and named by J. W. Rodger and T. E. Thorpe in 1888.[5][7]

They prepared it by heating arsenic trifluoride and thiophosphoryl chloride together in a sealed glass tube to 150 °C. Also produced in this reaction was silicon tetrafluoride and phosphorus fluorides. By increasing the PSCl
3 the proportion of PSF
3 was increased. They observed the spontaneous inflammability. They also used this method:

3 PbF
2 \+ P

5 → 3 PbS + PSF

at 170 °C, and also substituting a mixture of red phosphorus and sulfur, and substituting bismuth trifluoride.[5]

Another way to prepare PSF
3 is to add fluoride to PSCl
3 using sodium fluoride in acetonitrile.[8]

A high yield reaction can be used to produce the gas:[9][citation needed]

10 \+ 12 HF → 6 H
2S + 4 PSF

Under high pressure phosphorus trifluoride can react with hydrogen sulfide to yield:[10]

3 \+ H
2S → PSF
3 \+ H
2 (1350 bar at 200 °C)

Another high pressure production uses phosphorus trifluoride with sulfur.[10]

## Reactions

PSF
3 is decomposed by moisture and oxygen or heat. With heat, phosphorus, sulfur and phosphorus fluorides are formed:

PSF
3 → PF
3 \+ S

The hot gas reacts with glass producing SF
4, sulfur and elemental phosphorus. The pure gas is completely absorbed by alkali solutions. However, it does not react with ether, benzene, carbon disulfide, or pure sulfuric acid. It is stable against CaO, which can be used to remove impurities such as SiF
4 and PF
3. In air it burns spontaneously with a greyish green flame, producing solid white fumes. With dry oxygen combustion may not be spontaneous and the flame is yellow. On burning SO
2 and P

5 are produced. The gas burns with one of the coldest flames known.[5]

Reaction with water is slow:

PSF
3 \+ 4 H
2O → H
2S + H
3PO
4 \+ 3 HF

If PSF
3 is allowed to react with water in a lead glass container, the hydrofluoric acid and hydrogen sulfide combination produces a black deposit of lead sulfide on the inner surface of the glass.[5]

It reacts with four times its volume of ammonia gas producing ammonium fluoride and a mystery product, possibly P(NH

2SF.[5]

PSF
3 is an initiator for the polymerization of tetrahydrofuran.[11]

### Sulfur removal

2 PSF
3 \+ SO
2 → 2 POF
3 \+ 3 S

This reaction indicates why PSF
3 is not formed from PF
3 and SO
2.[10]

PSF
3 \+ SO
3 → POF
3 \+ 2 S and sulfur and sulfur sesquioxide (S2+
4 polysulfate) as additional products.[12][<span title="This chemical reaction is incorrect because there are 3 oxygens at the left side and 1 at the right side! Instead S at the right side should be SO? And what the hell is "S42+ polysulfate"??? (September 2023)">clarification needed]

### Fluorine substitution

PSF
3 \+ 2 ICl → PCl

3.[13][clarification needed]

PSF
3 combines with dimethylamine in solution to produce dimethylaminothiophosphoryl difluoride (H
3C–)
2N–P(=S)F
2 and difluorophosphate and hexafluorophosphate ions.[14]

Thiophosphoryl difluoride isocyanate can be formed by reacting PSF
3 with silicontetraisocyanate at 200 °C in an autoclave.[9]

### Cations

PSF
3 reacts with alkali solutions producing the fluoride and a thiophosphate (PSO3−
3).[5]

CsF \+ 2 PSF
3 → Cs[PF
6] + CsPS

2[15]

The reaction is showing the PSF
3 gas is related to the difluorodithiophosphate cation PS
2F−
2.[16]

The CsPS

2 is caesium difluorodithiophosphate.

PSF
3 reacts with [SF
6]−
in a mass spectrometer to form [PSF
4]−
.[17]

PSF
3 \+ [SF
6]−
→ [PSF
4]−
\+ SF

## Related compounds

One fluorine can be substituted by iodine to give thiophosphoryl difluoride iodide, PSIF
2.[18] PSIF
2 can be converted to hydrothiophosphoryldifluoride, S=PHF
2, by reducing it with hydrogen iodide.[19] In F
2P(=S)–S–PF
2, one sulfur forms a bridge between two phosphorus atoms.[18]

Dimethylaminothiophosphoryl difluoride ((H
3C–)
2N–P(=S)F
2) is a foul smelling liquid with a boiling point of 117 °C. It has a Trouton constant (entropy of vaporization at the boiling point of the liquid) of 24.4, and a heat of evaporation of 9530 cal/mole. Alternately it can be produced by fluorination of dimethylaminothiophosphoryl dichloride ((H
3C–)
2N–P(=S)Cl
2).

## Physical properties

The thiophosphoryl trifluoride molecule shape has been determined using electron diffraction. The interatomic distances are P=S 0.187±0.003 nm, P–F 0.153±0.002 nm and bond angles of F–P–F bonding is 100.3±2°, The microwave rotational spectrum has been measured for several different isotopologues.[20]

The critical point is at 346 K at 3.82 MPa.[21] The liquid refractive index is 1.353.[4]

The enthalpy of vaporisation 19.6 kJ/mol at boiling point.[22] The enthalpy of vaporisation at other temperatures is a function of temperature T: H(T)=28.85011(346-T)0.38 kJ/mol.[23]

The molecule is polar. It has a non-uniform distribution of positive and negative charge which gives it a dipole moment. When an electric field is applied more energy is stored than if the molecules did not respond by rotating. This increases the dielectric constant. The dipole moment of one molecule of thiophosphoryl trifluoride is 0.640 Debye.[24]

The infrared spectrum includes vibrations at 275, 404, 442, 698, 951 and 983 cm−1.[25] These can be used to identify the molecule.

## References

1. ↑ 1.0 1.1 A likely spelling mistake in Handbook of Chemistry and Physics 87 ed
2. ↑ "FP(F)(F)=S". http://www.chemicalize.org/structure/#!mol=FP(F)(F)=S&source=fp.
3. ↑ "phosphorothioic trifluoride". http://www.chemicalize.org/structure/#!mol=FP(F)(F)=S&source=fp.
4. ↑ 4.0 4.1 "Phosphorothioic trifluoride-(2404-52-6)-Chemical Dictionary-hgspace.com". http://hgspace.com/chemical-dictionary/cas/m5/2404-52-6.html.
5. ↑ 5.0 5.1 5.2 5.3 5.4 5.5 5.6 5.7 5.8 Thorpe, T. E.; Rodger, J. W. (1889). "XXXIV.?On thiophosphoryl fluoride". Journal of the Chemical Society, Transactions 55: 306–323. doi:10.1039/CT8895500306. https://zenodo.org/record/1754869.
6. ↑ Banks, Ronald Eric (2000). Fluorine chemistry at the millennium: fascinated by fluorine. Elsevier. p. 502. ISBN 0-08-043405-3. https://books.google.com/books?id=PKegfJ_fVBMC&pg=PA502.
7. ↑ Thorpe, T. E.; Rodger, J. W. (1888). "LX.?Thiophosphoryl fluoride". Journal of the Chemical Society, Transactions 53: 766–767. doi:10.1039/CT8885300766. https://zenodo.org/record/2173570.
8. ↑ Padma, D. K.; Vijayalakshmi, S. K.; Vasudevamurthy, A. R. (1976). "Investigations on the preparation, oxidation and reduction reactions of thiophosphoryl fluoride". Journal of Fluorine Chemistry 8 (6): 461. doi:10.1016/S0022-1139(00)81660-7.
9. ↑ 9.0 9.1 Roesky, H.W. (1970). "Thiophosphoryl-difluoride-isocyanate". Journal of Inorganic and Nuclear Chemistry 32 (6): 1845–1846. doi:10.1016/0022-1902(70)80591-7.
10. ↑ 10.0 10.1 10.2 Hagen, Arnulf P.; Callaway, Bill W. (1978). "High-pressure reactions of small covalent molecules. 10. The reaction of phosphorus trifluoride with hydrogen sulfide and sulfur dioxide". Inorganic Chemistry 17 (3): 554. doi:10.1021/ic50181a007.
11. ↑ Padma, D.K.; Vijayalakshmi, S.K. (1978). "Thiophosphoryl fluoride and phosphoryl fluoride as initiators for the polymerisation of tetrahydrofuran". Journal of Fluorine Chemistry 11: 51–56. doi:10.1016/S0022-1139(00)81597-3.
12. ↑ Sampath Kumar, H.P.; Padma, D.K.; Vasudeva Murthy, A.R. (1984). "Reaction of thiophosphoryl fluoride with sulphur trioxide". Journal of Fluorine Chemistry 26: 117–123. doi:10.1016/S0022-1139(00)85125-8.
13. ↑ Sampath Kumar, H.P.; Padma, D.K. (1990). "Reaction of phosphorus trifluoride and thiophosphoryl fluoride with iodine monochloride and oxidation of phosphorus trifluoride with nitryl chloride, iodic acid, periodic acid, sodium nitrite and potassium nitrite". Journal of Fluorine Chemistry 49 (3): 301. doi:10.1016/S0022-1139(00)85026-5.
14. ↑ Cavell, R. G. (1968). "Chemistry of phosphorus fluorides. Part III. The reaction of thiophosphoryl-fluoride with dimethylamine and some properties of the dimethylaminothio- phosphoryl fluorides". Canadian Journal of Chemistry 46 (4): 613–621. doi:10.1139/v68-100.
15. ↑ Roesky, Herbert W.; Tebbe, Fred N.; Muetterties, Earl L. (1970). "Thiophosphate chemistry. Anion set X2PS2−, (XPS2)2S2−, and (XPS2)2S22−". Inorganic Chemistry 9 (4): 831. doi:10.1021/ic50086a028.
16. ↑ Islam, Mohammad Q.; Hill, William E.; Webb, Thomas R. (1990). "Quadruply bonded dimolybdenum complexes of PF2S2−. Comparison with complexes of PR2S2p− (R = Et, Me)". Journal of Fluorine Chemistry 48 (3): 429. doi:10.1016/S0022-1139(00)80227-4.
17. ↑ Rhyne, T; Dillard, J (1971). "Reactions of gaseous inorganic negative ions: III. SF6− with POF3 and PSF3". International Journal of Mass Spectrometry and Ion Physics 7 (5): 371. doi:10.1016/0020-7381(71)85003-9. Bibcode: 1971IJMSI...7..371R.
18. ↑ 18.0 18.1 Charlton, Thomas L.; Cavell, Ronald G. (1969). "Difluorothiophosphoryl-μ-thio-difluorophosphine and difluorophosphoryl-μ-oxo-difluorophosphine. Novel mixed-valence fluorophosphorus compounds". Inorganic Chemistry 8 (11): 2436. doi:10.1021/ic50081a037.
19. ↑ Charlton, Thomas L.; Cavell, R. G. (1968). "Preparation and properties of iodothiophosphoryl difluoride, SPF2I". Inorganic Chemistry 7 (11): 2195. doi:10.1021/ic50069a005.
20. ↑ Williams, Quitman; Sheridan, John; Gordy, Walter (1952). "Microwave Spectra and Molecular Structures of POF3, PSF3, POCl3, and PSCl3". The Journal of Chemical Physics 20 (1): 164–167. doi:10.1063/1.1700162. Bibcode: 1952JChPh..20..164W.
21. ↑ Handbook of Chemistry and Physics 87 ed page 6-39
22. ↑ Mattox, D. M. (2003-12-31). The foundations of vacuum coating technology. Elsevier Science. p. 550. ISBN 978-0-8155-1495-4. https://books.google.com/books?id=31O4upzTHQwC&pg=PA550.
23. ↑ Mattox, D. M. (2003-12-31). The foundations of vacuum coating technology. Elsevier Science. p. 406. ISBN 978-0-8155-1495-4. https://books.google.com/books?id=31O4upzTHQwC&pg=PA406.
24. ↑ Mattox, D. M. (2003-12-31). The foundations of vacuum coating technology. Elsevier Science. p. 685. ISBN 978-0-8155-1495-4. https://books.google.com/books?id=31O4upzTHQwC&pg=PA685.
25. ↑ Cavell, R (1967). "The infrared spectrum of thiophosphoryl fluoride". Spectrochimica Acta Part A: Molecular Spectroscopy 23 (2): 249–256. doi:10.1016/0584-8539(67)80227-7. Bibcode: 1967AcSpA..23..249C.

## Other references

* Humphries, C. M.; Walsh, A. D.; Warsop, P. A. (1963). "Absorption spectrum of chlorine dioxide in the vacuum ultra-violet". Transactions of the Faraday Society 35: 137. doi:10.1039/df9633500137.
* Montana, Anthony J.; Zumbulyadis, Nikolaos; Dailey, Benjamin P. (1976). "19F and 31P magnetic shielding anisotropies and the F–P–F bond angle of PSF3 in a smectic liquid crystal solvent". The Journal of Chemical Physics 65 (11): 4756. doi:10.1063/1.432929. Bibcode: 1976JChPh..65.4756M.
* "Thiophosphoryl fluoride - CAS # 2404-52-6". http://www.caslab.com/Thiophosphoryl_fluoride_CAS_2404-52-6/.
* Hawkins, Norval John (1951). The structure of PSF3 and POF3 from microwave spectroscopy. https://books.google.com/books?id=0vv5GwAACAAJ.
* Chase, M. W. (1998). "Thiophosphoryl fluoride". NIST. pp. 1–1951. http://webbook.nist.gov/cgi/cbook.cgi?ID=C2404526&Units=SI&Mask=7.
* Williams, Quitman; Sheridan, John; Gordy, Walter (1952). "Microwave Spectra and Molecular Structures of POF3, PSF3, POCl3, and PSCl3". The Journal of Chemical Physics 20 (1): 164–167. doi:10.1063/1.1700162. Bibcode: 1952JChPh..20..164W.
* Lange, Willy; Askitopoulos, Konstantin (1938). "Zur Kenntnis des Phosphorsulfotrifluorids PSF3 und über ein Salz der Thiodifluorphosphorsäure H\PSF2O]". Berichte der Deutschen Chemischen Gesellschaft (A and B Series) 71 (4): 801. doi:10.1002/cber.19380710419.
* Poulenc, C. (1891). "Comptes rendus hebdomadaires des séances de l'Académie des sciences / Publiés... Par MM. Les secrétaires perpétuels". Comptes Rendus 113: 75. http://gallica.bnf.fr/ark:/12148/bpt6k30691/f75.image.

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