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Arsine

 

Arsine

Arsine
Arsine
Names
IUPAC names
Arsenic trihydride
Arsane
Trihydridoarsenic
Other names
Arseniuretted hydrogen,
Arsenous hydride,
hydrogen arsenide
Arsenic hydride
Identifiers
 Y
ChEBI  Y
ChemSpider  Y
EC number 232-066-3
Jmol-3D images Image
PubChem
Properties
AsH3
Molar mass 77.9454 g/mol
Appearance colourless gas
Density 4.93 g/l, gas; 1.640 g/mL (−64 °C)
Melting point −111.2 °C (−168.2 °F; 162.0 K)
Boiling point −62.5 °C (−80.5 °F; 210.7 K)
0.07 g/100 ml (25 °C)
Vapor pressure 14.9 atm[1]
Structure
trigonal pyramidal
0.20 D
Thermochemistry
223 J.K−1.mol−1
+66.4 kJ/mol
Hazards
Main hazards explosive, flammable, potential occupational carcinogen[1]
Safety data sheet See: data page
Very flammable (F+)
Highly toxic (T+)
Harmful (Xn)
Dangerous for the environment (N)
R-phrases R50/53
S-phrases (S1/2), S9, S16, S28, S33, S36/37, S45, S60, S61
NFPA 704
4
4
2
Flash point −62 °C (−80 °F; 211 K)
Explosive limits 5.1%-78%[1]
Lethal dose or concentration (LD, LC):
LD50 (Median dose)
2.5mg/kg(Intravenous)[2]
120 ppm (rat, 10 min)
77 ppm (mouse, 10 min)
201 ppm (rabbit, 10 min)
108 ppm (dog, 10 min)[3]
250 ppm (human, 30 min)
300 ppm (human, 5 min)
25 ppm (human, 30 min)[3]
US health exposure limits (NIOSH):
PEL (Permissible)
TWA 0.05 ppm (0.2 mg/m3)[1]
REL (Recommended)
C 0.002 mg/m3 [15-minute][1]
3 ppm[1]
Related compounds
Related hydrides
Ammonia; Phosphine; Stibine; Bismuthine
Supplementary data page
Refractive index (n),
Dielectric constantr), etc.
Thermodynamic
data
Phase behaviour
solid–liquid–gas
UV, IR, NMR, MS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
 N  (: Y/N?)

Arsine is an aryl or alkyl. For example, As(C6H5)3, called triphenylarsine, is referred to as "an arsine."

Contents

  • General properties 1
  • Discovery and synthesis 2
  • Reactions 3
    • Thermal decomposition 3.1
    • Oxidation 3.2
    • Precursor to metallic derivatives 3.3
    • Gutzeit test 3.4
    • Acid-base reactions 3.5
    • Reaction with halogen compounds 3.6
    • Catenation 3.7
  • Applications 4
    • Microelectronics applications 4.1
    • Chemical warfare 4.2
  • Forensic science and the Marsh test 5
  • Toxicology 6
    • Occupational exposure limits 6.1
  • See also 7
  • References 8
  • External links 9

General properties

At its standard state, arsine is a colorless, denser-than-air gas that is slightly soluble in garlic or fish-like scent when the compound is present above 0.5 ppm.[5] This compound is generally regarded as stable, since at room temperature it decomposes only slowly. At temperatures of ca. 230 °C decomposition to arsenic and hydrogen is rapid. Several factors, such as humidity, presence of light and certain catalysts (namely aluminium) facilitate the rate of decomposition.[6]

AsH3 is a pyramidal molecule with H–As–H angles of 91.8° and three equivalent As–H bonds, each of 1.519 Å length.[7]

Discovery and synthesis

AsH3 is generally prepared by the reaction of As3+ sources with H equivalents.[8]

4 AsCl3 + 3 NaBH4 → 4 AsH3 + 3 NaCl + 3 BCl3

As reported in 1775, Carl Scheele reduced arsenic(III) oxide with zinc in the presence of acid. This reaction is a prelude to the Marsh test, described below.

Alternatively, sources of As3− react with protonic reagents to also produce this gas:[9]

Zn3As2 + 6 H+ → 2 AsH3 + 3 Zn2+
Na3As + 3 HBr → AsH3 + 3 NaBr

Reactions

Our understanding of the chemical properties of AsH3 is well developed and can be anticipated based on an average of the behavior of PH3 and SbH3.

Thermal decomposition

Typical for a heavy hydride (e.g., SbH3, H2Te, SnH4), AsH3 is unstable with respect to its elements. In other words, AsH3 is stable kinetically but not thermodynamically.

2 AsH3 → 3 H2 + 2 As

This decomposition reaction is the basis of the Marsh Test described below, which detects the metallic As.

Oxidation

Continuing the analogy to SbH3, AsH3 is readily oxidized by concentrated O2 or the dilute O2 concentration in air:

2 AsH3 + 3 O2 → As2O3 + 3 H2O

Arsine will react violently in presence of strong oxidizing agents, such as potassium permanganate, sodium hypochlorite or nitric acid.[6]

Precursor to metallic derivatives

AsH3 is used as a precursor to metal complexes of "naked" (or "nearly naked") As. Illustrative is the dimanganese species [(C5H5)Mn(CO)2]2AsH, wherein the Mn2AsH core is planar.[10]

Gutzeit test

A characteristic test for arsenic involves the reaction of AsH3 with Ag+, called the Gutzeit test for arsenic.[11] Although this test has become obsolete in analytical chemistry, the underlying reactions further illustrate the affinity of AsH3 for "soft" metal cations. In the Gutzeit test, AsH3 is generated by reduction of aqueous arsenic compounds, typically arsenites, with Zn in the presence of H2SO4. The evolved gaseous AsH3 is then exposed to AgNO3 either as powder or as a solution. With solid AgNO3, AsH3 reacts to produce yellow Ag4AsNO3, whereas AsH3 reacts with a solution of AgNO3 to give black Ag3As.

Acid-base reactions

The acidic properties of the As–H bond are often exploited. Thus, AsH3 can be deprotonated:

AsH3 + NaNH2 → NaAsH2 + NH3

Upon reaction with the aluminium trialkyls, AsH3 gives the trimeric [R2AlAsH2]3, where R = (CH3)3C.[12] This reaction is relevant to the mechanism by which GaAs forms from AsH3 (see below).

AsH3 is generally considered non-basic, but it can be protonated by superacids to give isolable salts of the tetrahedral species [AsH4]+.[13]

Reaction with halogen compounds

Reactions of arsine with the halogens (fluorine and chlorine) or some of their compounds, such as nitrogen trichloride, are extremely dangerous and can result in explosions.[6]

Catenation

In contrast to the behavior of PH3, AsH3 does not form stable chains, although H2As–AsH2 and even H2As–As(H)–AsH2 have been detected. The diarsine is unstable above −100 °C.

Applications

Microelectronics applications

AsH3 is used in the synthesis of semiconducting materials related to microelectronics and solid-state lasers. Related to Phosphorus, Arsenic is an n-dopant for silicon and germanium.[6] More importantly, AsH3 is used to make the semiconductor GaAs by chemical vapor deposition (CVD) at 700–900 °C:

Ga(CH3)3 + AsH3 → GaAs + 3 CH4

For microelectronic applications, arsine can be provided via a sub-atmospheric gas source. In this type of gas package, the arsine is adsorbed on a solid microporous adsorbent inside a gas cylinder. This method allows the gas to be stored without pressure, significantly reducing the risk of an arsine gas leak from the cylinder. With this apparatus, arsine is obtained by applying vacuum to the gas cylinder valve outlet. For semiconductor manufacturing, this method is practical as these processes usually operate under high vacuum.

Chemical warfare

Since before lewisite (β-chlorovinyldichloroarsine), adamsite (diphenylaminechloroarsine), Clark I (diphenylchloroarsine) and Clark II (diphenylcyanoarsine) have been effectively developed for use in chemical warfare.[14]

Forensic science and the Marsh test

AsH3 is also well known in forensic science because it is a chemical intermediate in the detection of arsenic poisoning. The old (but extremely sensitive) Marsh test generates AsH3 in the presence of arsenic.[4] This procedure, developed around 1836 by James Marsh, is based upon treating an As-containing sample of a victim's body (typically the stomach) with As-free zinc and dilute sulfuric acid: if the sample contains arsenic, gaseous arsine will form. The gas is swept into a glass tube and decomposed by means of heating around 250–300 °C. The presence of As is indicated by formation of a deposit in the heated part of the equipment. On the other hand, the appearance of a black mirror deposit in the cool part of the equipment indicates the presence of antimony (the highly unstable SbH3 decomposes even at low temperatures).

The Marsh test was widely used by the end of the 19th century and the start of the 20th; nowadays more sophisticated techniques such as atomic spectroscopy, inductively coupled plasma and x-ray fluorescence analysis are employed in the forensic field. Though neutron activation analysis was used to detect trace levels of arsenic in the mid 20th century, it has since fallen out of use in modern forensics.

Toxicology

For the toxicology of other arsenic compounds, see Arsenic, Arsenic trioxide, and Arsenicosis.[13] The toxicity of arsine is distinct from that of other arsenic compounds. The main route of exposure is by inhalation, although poisoning after skin contact has also been described. Arsine attacks haemoglobin in the red blood cells, causing them to be destroyed by the body.[15][16]

The first signs of exposure, which can take several hours to become apparent, are headaches, vertigo and nausea, followed by the symptoms of haemolytic anaemia (high levels of unconjugated bilirubin), haemoglobinuria and nephropathy. In severe cases, the damage to the kidneys can be long-lasting.[1]

Exposure to arsine concentrations of 250 ppm is rapidly fatal: concentrations of 25–30 ppm are fatal for 30 min exposure, and concentrations of 10 ppm can be fatal at longer exposure times.[3] Symptoms of poisoning appear after exposure to concentrations of 0.5 ppm. There is little information on the chronic toxicity of arsine, although it is reasonable to assume that, in common with other arsenic compounds, a long-term exposure could lead to arsenicosis.

Occupational exposure limits

Country Limit[17]
Argentina Confirmed human carcinogen
Australia TWA 0.05 ppm (0.16 mg/m3)
Belgium TWA 0.05 ppm (0.16 mg/m3)
Bulgaria Confirmed human carcinogen
Colombia Confirmed human carcinogen
Denmark TWA 0.01 ppm (0.03 mg/m3)
Egypt TWA 0.05 ppm (0.2 mg/m3)
France VME 0.05 ppm (0.2 mg/m3)

VLE 0.2 ppm (0.8 mg/m3)

Hungary TWA 0.2 mg/m3STEL 0.8 mg/m3
Japan Occupational Exposure Limit 0.01 ppm (0.032 mg/m3)

Continuous 0.1 ppm (0.32 mg/m3)

Jordan Confirmed human carcinogen
Mexico TWA 0.05 ppm (0.2 mg/m3)
Netherlands MAC-TCG 0.2 mg/m3
New Zealand TWA 0.05 ppm (0.16 mg/m3)
Norway TWA 0.003 ppm (0.01 mg/m3)
Philippines TWA 0.05 ppm (0.16 mg/m3)
Poland TWA 0.2 mg/m3 STEL 0.6 mg/m3
Russia STEL 0.1 mg/m3
Singapore Confirmed human carcinogen
South Korea TWA 0.05 ppm (0.2 mg/m3)
Sweden TWA 0.02 ppm (0.05 mg/m3)
Switzerland MAK-week 0.05 ppm (0.16 mg/m3)
Thailand TWA 0.05 ppm (0.2 mg/m3)
Turkey TWA 0.05 ppm (0.2 mg/m3)
United Kingdom TWA 0.05 ppm (0.16 mg/m3)
United States 0.05 ppm (0.2 mg/m3)
Vietnam Confirmed human carcinogen

See also

References

  1. ^ a b c d e f g "NIOSH Pocket Guide to Chemical Hazards #0040".  
  2. ^ Levvy, G.A. (1946). "The Toxicity of Arsine Administered by Intraperitoneal Injection". Wiley Online Library. Retrieved 3 December 2014. 
  3. ^ a b c "Arsine". Immediately Dangerous to Life and Health.  
  4. ^ a b Holleman, A. F.; Wiberg, E. (2001) Inorganic Chemistry Academic Press: San Diego, ISBN 0-12-352651-5.
  5. ^ )"3"Medical Management Guidelines for Arsine (AsH. Agency for Toxic Substances & Disease Registry. 
  6. ^ a b c d Institut National de Recherche et de Sécurité (2000). "Fiche toxicologique nº 53: Trihydrure d'arsenic" ( 
  7. ^ Nielsen H. H. (1952). "The Molecular Structure of Arsine". The Journal of Chemical Physics 20 (12): 1955–1956.  
  8. ^ Bellama, J. M.; MacDiarmid, A. G. (1968). "Synthesis of the Hydrides of Germanium, Phosphorus, Arsenic, and Antimony by the Solid-Phase Reaction of the Corresponding Oxide with Lithium Aluminum Hydride". Inorganic Chemistry 7 (10): 2070–2.  
  9. ^ "Arsine" in Handbook of Preparative Inorganic Chemistry, 2nd ed., G. Brauer (ed.), Academic Press, 1963, NY, Vol. 1. p. 493.
  10. ^ Herrmann, W. A.; Koumbouris, B.; Schaefer, A.; Zahn, T.; Ziegler, M. L. (1985). "Generation and Complex Stabilization of Arsinidene and Diarsine Fragments by Metal-Induced Degradation of Monoarsine". Chemische Berichte 118 (6): 2472–88.  
  11. ^ King, E. J. (1959) Qualitative Analysis and Electrolytic Solutions Harcourt, Brace, and World; New York
  12. ^ Atwood, D. A.; Cowley, A. H.; Harris, P. R.; Jones, R. A.; Koschmieder, S. U.; Nunn, C. M.; Atwood, J. L.; Bott, S. G. (1993). "Cyclic Trimeric Hydroxy, Amido, Phosphido, and Arsenido Derivatives of aluminum and gallium. X-ray Structures of [tert-Bu2Ga(m-OH)]3 and [tert-Bu2Ga(m-NH2)]3". Organometallics 12: 24–29.  
  13. ^ a b R. Minkwitz, R.; Kornath, A.; Sawodny, W.; Härtner, H. (1994). "Über die Darstellung der Pnikogenoniumsalze AsH4+SbF6, AsH4+AsF6, SbH4+SbF6". Zeitschrift für anorganische und allgemeine Chemie 620 (4): 753–756.  
  14. ^ Suchard, Jeffrey R. (March 2006). "CBRNE — Arsenicals, Arsine". EMedicine. Retrieved 2006-09-05. 
  15. ^ Fowler B. A., Weissberg J. B. (1974). "Arsine poisoning". New England Journal of Medicine 300 (22): 1171–1174.  
  16. ^ Hatlelid K. M. (1996). "Reactions of Arsine with Hemoglobine". Journal of Toxicology and Environmental Health Part A 47 (2): 145–157.  
  17. ^ "Arsine". RTECS. National Institute for Occupational Safety and Health (NIOSH). 

External links

  • International Chemical Safety Card 0222
  • IARC Monograph "Arsenic and Arsenic Compounds"
  • NIOSH Pocket Guide to Chemical Hazards
  • Institut national de recherche et de sécurité (2000). "Trihydrure d'arsenic." Fiche toxicologique n° 53. Paris:INRS. (French)
  • Data on arsine from Air Liquide
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