Hydrogen thioperoxide

Hydrogen thioperoxide  |  |

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Names
IUPAC name

Sulfenic acid

Systematic IUPAC name

Thioperoxol

Other names

Sulfenic acid
oxadisulfane
Sulfur hydride hydroxide
Sulfonol
Sulfanol

Identifiers

CAS Number

* 62607-44-7

3D model (JSmol)

* Interactive image

ChEBI |

* CHEBI:37858

ChemSpider |

* 394637

Gmelin Reference

| 672

PubChem CID

* 447587

RTECS number |

* WP4100000

InChI

* InChI=1S/H2OS/c1-2/h1-2H

Key: RVEZZJVBDQCTEF-UHFFFAOYSA-N

SMILES

* OS

Properties

Chemical formula

| H2OS
Molar mass | 50.08 g·mol−1
Density | 1.249

Refractive index (nD)

| 1.484
Related compounds

Related compounds

* Hydrogen peroxide HOOH
* Hydrogen disulfide HSSH
* Hydroxylamine NH2OH
* Sulfoxylic acid HOSOH
* 1-oxatrisulfane HSSOH
* thiooxonium ylide H2OS[1]

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

Infobox references

Hydrogen thioperoxide, also called oxadisulfane or sulfanol, is the chemical with the structure H–S–O–H. It can be considered as the simple sulfur-substituted analog of the common hydrogen peroxide (H–O–O–H) chemical, and as the simplest hydrogen chalcogenide containing more than one type of chalcogen. The chemical has been described as the "missing link" between hydrogen peroxide and hydrogen disulfide (H–S–S–H),[2] though it is substantially less stable than either of the other two. It is the inorganic parent structure of the sulfenic acid class of organic compounds (R–S–O–H) and also the oxadisulfide linkage (R1–S–O–R2), where "R" is any organic structure. Sulfur is present in oxidation state 0\.

## Contents

* 1 Formation
* 2 Properties
* 3 Reactions
* 4 References

## Formation

Hydrogen thioperoxide has been synthesized in labs by photolysis of a mixture of ozone and hydrogen sulfide frozen in argon at 8 K[3] and by pyrolysis of Di-tert-butyl sulfoxide ({{{2}}}).[2][4] Yet another synthesis is by an electric discharge through water and sulfur.[5]

In the interstellar medium there is a hypothesis that hydrogen thioperoxide is formed in a reaction of sulfur monoxide with the trihydrogen cation, dihydrogen and an electron. Another possible route is sulfur monoxide reacting with atomic hydrogen to form HOS and HSO which in turn can add another hydrogen atom. However this mechanism probably needs a dust grain to take away excess energy.[6]

## Properties

Hydrogen thioperoxide molecules have a gauche conformation.[7] They are asymmetrical, but have a low barrier to convert from left-hand to right-hand forms, so that the molecule can tunnel between the forms.[5]

The measurements of the bond-lengths in hydrogen thioperoxide are H–S 1.3420 Å, S–O 1.6616 Å, O–H 0.9606 Å. The bond angles are H–S–O 98.57°, S–O–H 107.19°. The H–S and O–H bonds are twisted at 90.41°.[8]

The half-life of hydrogen thioperoxide in water is 40 minutes, much longer than the expected half-life of less than seconds for a sulfenic acid.[9] In the gas phase at high temperature and low pressure, it has a lifetime on the order of 5 seconds.[2] Its decomposition products include disulfur monoxide and molecular hydrogen.[2]

## Reactions

Two molecules of hydrogen thioperoxide can undergo cyclocondensation to form sulfinothioic acid HS(=O)SH and water.[10]

Hydrosulfide HS−
can react with HSOH to yield disulfane HSSH.[11]

## References

1. ↑ Iraqi, Muhammad; Schwarz, Helmut (April 1994). "Experimental evidence for the gas phase existence of HSOH (hydrogen thioperoxide) and SOH2 (thiooxonium ylide)". Chemical Physics Letters 221 (5–6): 359–362. doi:10.1016/0009-2614(94)00293-2. Bibcode: 1994CPL...221..359I.
2. ↑ 2.0 2.1 2.2 2.3 Winnewisser, G.; Lewen, F.; Thorwirth, S.; Behnke, M.; Hahn, J.; Gauss, J.; Herbst, E. (2003). "Gas-Phase Detection of HSOH: Synthesis by Flash Vacuum Pyrolysis of Di-tert-butyl Sulfoxide and Rotational-Torsional Spectrum". Chem. Eur. J. 9 (22): 5501–5510. doi:10.1002/chem.200305192. PMID 14639633. Bibcode: 2003CEJ.....9.5501W.
3. ↑ Smardzewski1, R.R.; Lin, M.C. (1977). "Matrix reactions of oxygen atoms with H2S molecules". J. Chem. Phys. 66 (7): 3197–3204. doi:10.1063/1.434294. Bibcode: 1977JChPh..66.3197S.
4. ↑ Beckers, H.; Esser, S.; Metzroth, T.; Behnke, M.; Willner, H.; Gauss, J.; Hahn, J. (2006). "Low-Pressure Pyrolysis of tBu2SO: Synthesis and IR Spectroscopic Detection of HSOH". Chem. Eur. J. 12 (3): 832–844. doi:10.1002/chem.200500104. PMID 16240313.
5. ↑ 5.0 5.1 Baum, Oliver (2008) (in en). HSOH: An Elusive Species with Many Different Traits. Cuvillier Verlag. pp. 1–2. ISBN 9783867277907. https://www.uni-kassel.de/fb10/fileadmin/datas/fb10/physik/laborastrophysik/Dokumente/Paper_TGi/Dissertation_Baum_Oliver_2008.pdf. Retrieved 2017-03-11.
6. ↑ Baum 70-73
7. ↑ Cárdenas-Jirón, G.I.; Letelier, J.R.; Toro-Labbé, A. (1998). "The Internal Rotation of Hydrogen Thioperoxide: Energy, Chemical Potential, and Hardness Profiles". J. Phys. Chem. A 102 (40): 7864–7871. doi:10.1021/jp981841j. Bibcode: 1998JPCA..102.7864C.
8. ↑ Baum 84
9. ↑ Kumar, Murugaeson R.; Farmer, Patrick J. (2018). "Chemical trapping and characterization of small oxoacids of sulfur (SOS) generated in aqueous oxidations of H2S". Redox Biology 14: 485–491. doi:10.1016/j.redox.2017.10.012. PMID 29096321.
10. ↑ Freeman, Fillmore; Bui, An; Dinh, Lauren; Hehre, Warren J. (2 August 2012). "Dehydrative Cyclocondensation Mechanisms of Hydrogen Thioperoxide and of Alkanesulfenic Acids". The Journal of Physical Chemistry A 116 (30): 8031–8039. doi:10.1021/jp3024827. PMID 22724673. Bibcode: 2012JPCA..116.8031F.
11. ↑ Kolloru, Gopi K. (25 February 2015) (in en). Hydrogen Sulfide in Redox Biology. Academic Press. p. 274. ISBN 9780128016237. https://books.google.com/books?id=xO6cBAAAQBAJ&pg=PA274.

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Hydrogen compounds

* H3AsO3
* H3AsO4
* HArF
* HAt
* HSO3F
* HBF4
* HBr
* HBrO
* HBrO2
* HBrO3
* HBrO4
* HCl
* HClO
* HClO2
* HClO3
* HClO4
* HCN
* HCNO
* H2CrO4/H2Cr2O7
* H2CO3
* H2CS3
* HF
* HFΟ
* HI
* HIO
* HIO2
* HIO3
* HIO4
* HMnO4
* H2MoO4
* HNC
* NaHCO3
* HNCO
* HNO
* HNO2
* HNO3
* H2N2O2
* HNO5S
* H3NSO3
* H2O
* H2O2
* H2O3
* H3PO2
* H3PO3
* H3PO4
* H4P2O7
* H5P3O10
* H2PtCl6
* H2S
* H2S2
* H2Se
* H2SeO3
* H2SeO4
* H4SiO4
* H2SiF6
* HSCN
* HNSC
* H2SO3
* H2SO4
* H2SO5
* H2S2O3
* H2S2O6
* H2S2O7
* H2S2O8
* CF3SO3H
* H2Te
* H2TeO3
* H6TeO6
* H4TiO4
* H2Po
* HCo(CO)4

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Sulfur compounds

* Al2S3
* As2S2
* As2S3
* As2S5
* As4S4
* Au2S
* Au2S3
* B2S3
* BaS
* BeS
* Bi2S3
* Br2S
* Br2S2
* CS2
* C3S2
* C6S6
* CaS
* CdS
* CeS
* SCl2
* S2Cl2
* CoS
* Cr2S3
* CuS
* D2S
* Dy2S3
* Er2S3
* EuS
* SF4
* S2F10
* SF6
* FeS2
* GaS
* H2S
* HfS2
* HgS
* InS
* I2S
* LaS
* LiS
* MgS
* MoS3
* NiS
* SO2
* SO3
* P4S7
* PbS
* PbS2
* PtS
* ReS2
* SrS
* TlS
* SV
* SeS2
* S2U
* WS2
* Sb2S3
* Sb2S5
* Sm2S3
* Y2S3
* Ag2SO4
* SOBr2
* CSTe
* C2H4S
* C2H6S3
* C4H4S
* CaSO4
* C32H66S2
* CuFeS2
* H2SO4
* H2SO3
* F2OS
* NaHS
* K2SO3
* O3S3Sb4
* Yb2(SO4)3
* AlKO8S2
* CHCl3S
* KSCN
* CdSO3
* PSCl3
* SOCl2
* Cs2O4S
* Re2S7
* Na2S
* K2S
* H2S2O7
* H2SO5
* NH5S
* HgSO4
* K2SO4
* RaSO4
* SnSO4
* SrSO4
* Zr(SO4)2
* Ti(SO4)2
* Tm2(SO4)3
* AlNa(SO4)2
* Er2(SO4)3
* Eu2(SO4)3
* CHNS
* Co(SCN)2
* C2H3SN
* PSI3
* ZrS2
* SiS
* CSSe

Chemical formulas

Template:Peroxides

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