Jump to content

Arsenic pentasulfide

From Wikipedia, the free encyclopedia
Arsenic pentasulfide
Names
IUPAC name
Arsenic pentasulfide
Other names
Arsenic(V) sulfide
Diarsenic pentasulfide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.154.195Edit this at Wikidata
EC Number
  • 625-728-1
UNII
UN number 1557
  • InChI=1S/As2S5/c3-1(4)7-2(5)6checkY
    Key: AYRZLUSHOXJGKY-UHFFFAOYSA-NcheckY
  • InChI=1S/As4S10/c5-1-9-2(6)12-3(7,10-1)14-4(8,11-1)13-2
    Key: CHQYGMAMCBQSIU-UHFFFAOYSA-N
  • S=[As](=S)S[As](=S)=S
  • S=[As]12S[As]3(=S)S[As](=S)(S1)S[As](=S)(S2)S3
Properties
As2S5
Molar mass 310.14g·mol−1
Appearance Vivid, dark orange, opaque crystals
Melting point 300 °C (572 °F; 573 K)(minimum)
Boiling point 500 °C (932 °F; 773 K)(decomposes)
0.014 g dm−3(at 0 °C)
Hazards
GHSlabelling:
GHS06: ToxicGHS09: Environmental hazard
Danger
H301,H331,H410
P261,P264,P270,P271,P273,P301+P310,P304+P340,P311,P321,P330,P391,P403+P233,P405,P501
Related compounds
Related compounds
Arsenic pentoxide

Arsenic trisulfide
Phosphorus pentasulfide

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

Arsenic pentasulfideis aninorganic compoundcontaining arsenic and sulfur.[1]

Uses

[edit]

Solids of the approximate formulaAs2S5have been used aspigmentsand chemical intermediates but are generally only of interest in academic laboratories.[2]

Preparation

[edit]

Arsenic pentasulfide is prepared by precipitation from an acidic solution of soluble As(V) salts by treatment withhydrogen sulfide.[3]It may be also prepared by heating a mixture of arsenic and sulfur, extracting the fused mass with anammoniasolution and reprecipitating arsenic pentasulfide at low temperature by addition ofhydrochloric acid.

Phosphorus pentasulfidewith the formula P4S10,is a molecular compound featuring tetrahedral phosphorus(V) centres. Trends in arsenic redox potentials suggest that As2S5adopts a similar structure, a plausible alternative being an arsenic polysulfide.

Reactions

[edit]

Arsenic pentasulfide hydrolyzes in boiling water, givingarsenous acidandsulfur:

As2S5+ 6 H2O → 2 H3AsO3+ 2 S + 3 H2S

It oxidizes in air at elevated temperatures producing arsenic oxides, the products and yields of which are variable. In alkali metal sulfide solutions arsenic pentasulfide forms athioarsenateanion, [AsS4]3−,which contain As(V) centres.

References

[edit]
  1. ^Greenwood, Norman N.;Earnshaw, Alan (1997).Chemistry of the Elements(2nd ed.).Butterworth-Heinemann.ISBN978-0-08-037941-8.
  2. ^A. L. Emelina, A. S. Alikhanian, A. V. Steblevskii and E. N. Kolosov "Phase diagram of the As-S system" Inorganic Materials, 2007, Volume 43, pages95-104,doi:10.1134/S002016850702001X
  3. ^Norman., N. C., ed. (1998).Chemistry of arsenic, antimony and bismuth.London: Blackie Acad. & Professional. pp. 114–115.ISBN978-0-7514-0389-3.