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Potassium hydrosulfide

From Wikipedia, the free encyclopedia
Potassium hydrosulfide
K+SH
Names
IUPAC name
Potassium hydrosulfide
Other names
Potassium bisulfide, Potassium sulfhydrate, potassium hydrogen sulfide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.013.803Edit this at Wikidata
EC Number
  • 215-182-9
UNII
  • InChI=1S/K.H2S/h;1H2/q+1;/p-1 ☒N
    Key: ZOCLAPYLSUCOGI-UHFFFAOYSA-M ☒N
  • InChI=1/K.H2S/h;1H2/q+1;/p-1
    Key: ZOCLAPYLSUCOGI-REWHXWOFAJ
  • [SH-].[K+]
Properties
KSH
Molar mass72.171 g/mol
Appearancewhite solid
Density1.68–1.70 g/cm3
Melting point455 °C (851 °F; 728 K)
good
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Flammable solid, stench, releaseshydrogen sulfide
NFPA 704 (fire diamond)
Related compounds
Otheranions
Potassium hydroxide
Othercations
Sodium hydrosulfide
Related compounds
potassium sulfide
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound

Potassium hydrosulfide is aninorganic compound with the formula KSH. This colourlesssalt consists of the cationK+ and thebisulfide anion[SH]. It is the product of the half-neutralization ofhydrogen sulfide withpotassium hydroxide. The compound has been used in the synthesis oforganosulfur compounds.[1] Aqueous solutions ofpotassium sulfide consist of a mixture of potassium hydrosulfide andpotassium hydroxide.

Atomic structure of crystalline KSH according toX-ray crystallography. Color code: violet = K, yellow = S, white = H.

The structure of the potassium hydrosulfide resembles that ofpotassium chloride. Their structure is however complicated by the non-spherical symmetry of theSHanions, but these tumble rapidly in the solid.[2]

Potassium hydrosulfide reacts with elemental sulfur to gives polysulfide salts, such asdipotassium pentasulfide.

Synthesis

[edit]

Potassium hydrosulfide is prepared by neutralizing aqueousKOH withH2S.[3][4]

References

[edit]
  1. ^Dittmer, Donald C. (2001). "Potassium Hydrogen Sulfide". In Paquette, L. (ed.).Encyclopedia of Reagents for Organic Synthesis. J. Wiley & Sons, New York.doi:10.1002/047084289X.rp227.ISBN 0471936235.
  2. ^Haarmann, F; Jacobs, H.; Roessler, E.; Senker, J. (2002)."Dynamics of Anions and Cations in Hydrogensulfides of Alkali Metals (NaHS, KHS, RbHS): A Proton Nuclear Magnetic Resonance Study".Journal of Chemical Physics.117 (3):1269–1276.Bibcode:2002JChPh.117.1269H.doi:10.1063/1.1483860.
  3. ^Kurzer, F.; Lawson, A. (1962)."Thiobenzoylthioglycolic Acid".Organic Syntheses.42: 100.doi:10.15227/orgsyn.042.0100.
  4. ^Robert L. Frank and James R. Blegen (1948). "Benzoyl Disulfide".Organic Syntheses.28: 16.doi:10.15227/orgsyn.028.0016.
H, (pseudo)halogens
chalcogens
pnictogens
B, C group
transition metals
organic
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