| Arsenic trisulfide | |
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Arsenic trisulfide |
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Other names
Arsenic(III) sulfide |
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| Identifiers | |
| CAS number | 1303-33-9 |
| PubChem | 4093503 |
| ChemSpider | 21241348 |
| UNII | 44SIJ800OX |
| EC number | 215-117-4 |
| RTECS number | CG2638000 |
| Jmol-3D images | Image 1 |
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| Properties | |
| Molecular formula | As2S3 |
| Molar mass | 246.04 g mol−1 |
| Exact mass | 245.759404904 g mol-1 |
| Appearance | Orange crystals |
| Density | 3.43 g cm-3 |
| Melting point |
310 °C, 583 K, 590 °F |
| Boiling point |
707 °C, 980 K, 1305 °F |
| Structure | |
| Space group | P21/n (No. 11) |
| Lattice constant | a = 1147.5(5) pm, b = 957.7(4) pm, c = 425.6(2) pm |
| Lattice constant | α = 90°, β = 90.68(8)°, γ = 90° |
| pyramidal (As) | |
| Hazards[1][2] | |
| GHS pictograms | |
| GHS signal word | DANGER |
| GHS hazard statements | H300, H331, H400, H411 |
| EU Index | 033-002-00-5 |
| NFPA 704 |
0
3
0
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| U.S. Permissible exposure limit (PEL) |
0.01 mg m−3 TWA (as As) |
| Related compounds | |
| Other anions | Arsenic trioxide Arsenic triselenide |
| Other cations | Phosphorus trisulfide Antimony trisulfide Bismuth sulfide |
| Related compounds | Tetraarsenic tetrasulfide |
| (verify) (what is: /?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| Infobox references | |
Arsenic trisulfide is the inorganic compound with the formula As2S3. This bright yellow solid is a well known mineral orpiment (Latin: auripigment), has been used as a pigment, and has played a role in the analysis of arsenic compounds. This chalcogenide material is a group V/VI, intrinsic p-type semiconductor and exhibits photo-induced phase-change properties. The other principal arsenic sulfide is realgar, As4S4, which is red-orange and also occurs as a mineral.
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As2S3 occurs both in crystalline and amorphous forms. Both forms feature polymeric structures consisting trigonal pyramidal As(III) centres linked by sulfide centres. The sulfide centres are two-fold coordinated to two arsenic atoms. In the crystalline form, the compound adopts a ruffled sheet structure.[3] The bonding between the sheets consists of van der Waals forces. The crystalline form is usually found in geological samples. Amorphous As2S3 does not possess a layered structure but is more highly cross-linked. Like other glasses, there is no medium or long-range order, but the first co-ordination sphere is well defined. As2S3 is a good glass former and exhibits a wide glass-forming region in its phase diagram.
Amorphous As2S3 is obtained via the fusion of the elements at 390 °C. Rapid cooling of the reaction melt ensures the disordered arrangement of the bonds, resulting in the glass. The reaction can be represented with the chemical equation:
Upon heating in a vacuum, polymeric As2S3 "cracks" to give a mixture of molecular species, including molecular As4S6.[4][5] As4S6 adopts the adamantane geometry, like that observed for P4O6 and As4O6. When a film of this material is exposed to an external energy source such as thermal energy (via thermal annealing [6]), electromagnetic radiation (i.e. UV lamps, lasers,[7] electron beams)[8]), As4S6 polymerizes:
As2S3 forms when aqueous solutions containing As(III) are treated with H2S. Arsenic was in the past analyzed and assayed by this reaction, which results in the precipitation of As2S3, which is then weighed. As2S3 can even be precipitated in 6M HCl. As2S3 is so insoluble that it is not toxic. As2S3 characteristically dissolves upon treatment with aqueous solutions containing sulfide ions. The dissolved arsenic species is the pyramidal trianion AsS3−
3:
As2S3 is the anhydride of the hypothetical thioarsenous acid, As(SH)3. Upon treatment with polysulfide ions, As2S3 dissolves to give a variety of species containing both S-S and As-S bonds. One derivative is S7As-S-, a ring that contains an exocyclic sulfido center attached to the As atom. As2S3 also dissolves in strongly alkaline solutions to give a mixture of AsS3−
3 and AsO3−
3.[9]
"Roasting" As2S3 in air gives volatile, toxic derivatives, this conversion being one of the hazards associated with the refining of heavy metal ores:
Due to its high refractive index of 2.45 and its large Knoop hardness compared to organic photoresists, As2S3 has been investigated for the fabrication of photonic crystals with a full-photonic band-gap. Advances in laser patterning techniques such as three-dimensional direct laser writing (3-D DLW) and chemical wet-etching chemistry, has allowed this material to be used as a photoresist to fabricate 3-D nanostructures.[10][11]
As2S3 has been investigated for use as a high resolution photoreist material since the early 1970s,[12][13] using aqueous etchants. Although these aqueous etchants allowed for low-aspect ratio 2-D structures to be fabricated, they do not allow for the etching of high aspect ratio structures with 3-D periodicity. Certain organic reagents, used in organic solvents, permit the high-etch selectivity required to produce high-aspect ratio structures with 3-D periodicity.
As2S3 and As4S4 have been investigated as treatments for acute promyelocytic leukemia (APL).[14] The mode of action is thought to be similar to that for As2O3.
Arsenic trisulfide manufactured into amorphous form is used as a chalcogenide glass for infrared optics. It is transparent between 620 nm and 11 µm. The arsenic trisulfide glass is more resistant to oxidation than crystalline arsenic trisulfide, which minimizes toxicity concerns.[15] It can be also used as an acousto-optic material.
The ancient Egyptians reportedly used orpiment, natural or synthetic, as a pigment in artistry and cosmetics.
Arsenic trisulfide is also used as a tanning agent. It was formerly used with indigo dye for the production of pencil blue, which allowed dark blue hues to be added to fabric via pencil or brush.
Precipitation of arsenic trisulfide is used as an analytical test for presence of dissimilatory arsenic-reducing bacteria (DARB).[16]
As2S3 is so insoluble that its toxicity is low. Aged samples can contain substantial amounts of arsenic oxides, which are soluble and therefore highly toxic.
Orpiment is found in volcanic environments, often together with other arsenic sulfides, mainly realgar. It is sometimes found in low-temperature hydrothermal veins, together with some other sulfide and sulfosalt minerals.
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