Arsenide: Difference between revisions
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Monatomic anion compounds |
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[[Image:Nickeline.jpg|thumb|220px|right|Nickel arsenide is a common impurity in ores of nickel. It is also a prototype of a class of structures.]] |
[[Image:Nickeline.jpg|thumb|220px|right|Nickel arsenide is a common impurity in ores of nickel. It is also a prototype of a class of structures.]] |
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==III–V |
==III–V compounds== |
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{{main|List of semiconductor materials}} |
{{main|List of semiconductor materials}} |
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Many arsenides of the [[group 13 elements]] (group III) are valuable semiconductors. [[Gallium arsenide]] (GaAs) features isolated arsenic centers with a [[Zincblende (crystal structure)|zincblende]] structure ([[wurtzite]] structure can eventually also form in nanostructures), and with predominantly covalent bonding – it is a III–V semiconductor. |
Many arsenides of the [[group 13 elements]] (group III) are valuable semiconductors. [[Gallium arsenide]] (GaAs) features isolated arsenic centers with a [[Zincblende (crystal structure)|zincblende]] structure ([[wurtzite]] structure can eventually also form in nanostructures), and with predominantly covalent bonding – it is a III–V semiconductor. |
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==II–V compounds== |
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{{main|:Category:II-V compounds}} |
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Arsenides of the [[group 12 elements]] (group II) are also noteworthy. [[Cadmium arsenide|Cadmium arsenide (Cd<sub>3</sub>As<sub>2</sub>)]] was shown to be a three-dimensional (3D) topological Dirac [[semimetal]] analogous to [[graphene]].<ref>{{Cite journal | doi = 10.1038/ncomms4786| pmid = 24807399| title = Observation of a three-dimensional topological Dirac semimetal phase in high-mobility Cd<sub>3</sub>As<sub>2</sub>| journal = Nature Communications| volume = 5| pages = 3786| year = 2014| last1 = Neupane | first1 = M. | last2 = Xu | first2 = S. Y. | last3 = Sankar | first3 = R. | last4 = Alidoust | first4 = N. | last5 = Bian | first5 = G. | last6 = Liu | first6 = C. | last7 = Belopolski | first7 = I. | last8 = Chang | first8 = T. R. | last9 = Jeng | first9 = H. T. | last10 = Lin | first10 = H. | last11 = Bansil | first11 = A. | last12 = Chou | first12 = F. | last13 = Hasan | first13 = M. Z. | bibcode = 2014NatCo...5.3786N| arxiv = 1309.7892 | s2cid = 32847905}}</ref><ref name=doi3990>{{Cite journal | doi = 10.1038/nmat3990| pmid = 24859642| title = A stable three-dimensional topological Dirac semimetal Cd<sub>3</sub>As<sub>2</sub>| journal = Nature Materials| volume = 13| issue = 7| pages = 677–81| year = 2014| last1 = Liu | first1 = Z. K.| last2 = Jiang | first2 = J.| last3 = Zhou | first3 = B.| last4 = Wang | first4 = Z. J.| last5 = Zhang | first5 = Y.| last6 = Weng | first6 = H. M.| last7 = Prabhakaran | first7 = D.| last8 = Mo | first8 = S. K. | last9 = Peng | first9 = H.| last10 = Dudin | first10 = P.| last11 = Kim | first11 = T.| last12 = Hoesch | first12 = M.| last13 = Fang | first13 = Z.| last14 = Dai | first14 = X.| last15 = Shen | first15 = Z. X.| last16 = Feng | first16 = D. L.| last17 = Hussain | first17 = Z.| last18 = Chen | first18 = Y. L.| bibcode = 2014NatMa..13..677L}}</ref> Cd<sub>3</sub>As<sub>2</sub>, [[Zinc arsenide|Zn<sub>3</sub>As<sub>2</sub>]] and other compounds of the [[Zinc cadmium phosphide arsenide|Zn-Cd-P-As quaternary system]] have very similar crystalline structures, which can be considered distorted mixtures of the zincblende and [[Fluorite structure|antifluorite]] crystalline structures.<ref>{{Cite journal|title=Compounds and solid solutions of the Zn-Cd-P-As system in semiconductor electronics|journal=Inorganic Materials|last1=Trukhan|first1=V. M.|volume=50|pages=868–873|last2=Izotov|first2=A. D.|issue=9|doi=10.1134/S0020168514090143|year=2014|last3=Shoukavaya|first3=T. V.|s2cid=94409384}}</ref> |
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==Polyarsenides== |
==Polyarsenides== |
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===Transition metal arsenides=== |
===Transition metal arsenides=== |
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Arsenic anionics are known to catenate, that is, form chains, rings, and cages. The mineral [[skutterudite]] (CoAs<sub>3</sub>) features rings that are usually described as {{chem|As|4|4-}}.<ref name="Greenwood"/> Assigning formal [[oxidation numbers]] is difficult because these materials are highly covalent and often are best described with [[band theory]]. [[Sperrylite]] (PtAs<sub>2</sub>) is usually described as {{chem|Pt|4+|As|2|4−}}. The arsenides of the transition metals are mainly of interest because they contaminate sulfidic ores of commercial interest. The extraction of the metals – nickel, iron, cobalt, copper – entails chemical processes such as smelting that poses environmental risks. In the mineral, arsenic is immobile and poses no environmental risk. |
Arsenic anionics are known to catenate, that is, form chains, rings, and cages. The mineral [[skutterudite]] (CoAs<sub>3</sub>) features rings that are usually described as {{chem|As|4|4-}}.<ref name="Greenwood"/> Assigning formal [[oxidation numbers]] is difficult because these materials are highly covalent and often are best described with [[band theory]]. [[Sperrylite]] (PtAs<sub>2</sub>) is usually described as {{chem|Pt|4+|As|2|4−}}. The arsenides of the transition metals are mainly of interest because they contaminate sulfidic ores of commercial interest. The extraction of the metals – nickel, iron, cobalt, copper – entails chemical processes such as smelting that poses environmental risks. In the mineral, arsenic is immobile and poses no environmental risk. Released from the mineral, arsenic is poisonous and mobile. |
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===Zintl phases=== |
===Zintl phases=== |
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[[File:423080Asonly.png|thumb|right|Structure of [As<sub>7</sub>]<sup>3−</sup> subunit in the [[Zintl phase]] Cs<sub>2</sub>NaAs<sub>7</sub>.<ref>{{cite journal|title=New compounds with (As<sub>7</sub>)<sup>3−</sup> Clusters: Synthesis and Crystal Structures of the Zintl Phases Cs<sub>2</sub>NaAs<sub>7</sub>, Cs<sub>4</sub>ZnAs<sub>14</sub> and Cs<sub>4</sub>CdAs<sub>14</sub>| |
[[File:423080Asonly.png|thumb|right|Structure of [As<sub>7</sub>]<sup>3−</sup> subunit in the [[Zintl phase]] Cs<sub>2</sub>NaAs<sub>7</sub>.<ref>{{cite journal|title=New compounds with (As<sub>7</sub>)<sup>3−</sup> Clusters: Synthesis and Crystal Structures of the Zintl Phases Cs<sub>2</sub>NaAs<sub>7</sub>, Cs<sub>4</sub>ZnAs<sub>14</sub> and Cs<sub>4</sub>CdAs<sub>14</sub>|author1=He, Hua |author2=Tyson, C.-T. |author3=Bobev, S. |journal=Crystals|year=2011|volume=1|issue=3|pages=87–p98|doi=10.3390/cryst1030087|doi-access=free}}</ref>]] |
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Partial reduction of arsenic with alkali metals (and related electropositive elements) affords polyarsenic compounds, which are members of the [[Zintl phase]]s. |
Partial reduction of arsenic with alkali metals (and related electropositive elements) affords polyarsenic compounds, which are members of the [[Zintl phase]]s. |
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{{Reflist}} |
{{Reflist}} |
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{{Arsenides}} |
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==External links== |
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{{Monatomic anion compounds}} |
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[[Category:Anions]] |
[[Category:Anions]] |
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[[Category:Arsenides| ]] |
[[Category:Arsenides| ]] |
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[[Category:Arsenic( |
[[Category:Arsenic(−III) compounds]] |
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{{Inorganic-compound-stub}} |
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Latest revision as of 20:12, 8 September 2023
| Identifiers | |
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3D model (JSmol)
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| ChemSpider | |
CompTox Dashboard (EPA)
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| Properties | |
| As3− | |
| Molar mass | 74.921595 g·mol−1 |
| Related compounds | |
Other anions
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Phosphide Antimonide Bismuthide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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In chemistry, an arsenide is a compound of arsenic with a less electronegative element or elements. Many metals form binary compounds containing arsenic, and these are called arsenides. They exist with many stoichiometries, and in this respect arsenides are similar to phosphides.[1]
Alkali metal and alkaline earth arsenides
[edit]The group 1 alkali metals and the group 2, alkaline earth metals, form arsenides with isolated arsenic atoms. They form upon heating arsenic powder with excess sodium gives sodium arsenide (Na3As). The structure of Na3As is complex with unusually short Na–Na distances of 328–330 pm which are shorter than in sodium metal. This short distance indicates the complex bonding in these simple phases, i.e. they are not simply salts of As3− anion, for example.[1] The compound LiAs, has a metallic lustre and electrical conductivity indicating some metallic bonding.[1] These compounds are mainly of academic interest. For example, "sodium arsenide" is a structural motif adopted by many compounds with the A3B stoichiometry.
Indicative of their salt-like properties, hydrolysis of alkali metal arsenides gives arsine:
- Na3As + 3 H2O → AsH3 + 3 NaOH
III–V compounds
[edit]Many arsenides of the group 13 elements (group III) are valuable semiconductors. Gallium arsenide (GaAs) features isolated arsenic centers with a zincblende structure (wurtzite structure can eventually also form in nanostructures), and with predominantly covalent bonding – it is a III–V semiconductor.
II–V compounds
[edit]Arsenides of the group 12 elements (group II) are also noteworthy. Cadmium arsenide (Cd3As2) was shown to be a three-dimensional (3D) topological Dirac semimetal analogous to graphene.[2][3] Cd3As2, Zn3As2 and other compounds of the Zn-Cd-P-As quaternary system have very similar crystalline structures, which can be considered distorted mixtures of the zincblende and antifluorite crystalline structures.[4]
Polyarsenides
[edit]Transition metal arsenides
[edit]Arsenic anionics are known to catenate, that is, form chains, rings, and cages. The mineral skutterudite (CoAs3) features rings that are usually described as As4−
4.[1] Assigning formal oxidation numbers is difficult because these materials are highly covalent and often are best described with band theory. Sperrylite (PtAs2) is usually described as Pt4+
As4−
2. The arsenides of the transition metals are mainly of interest because they contaminate sulfidic ores of commercial interest. The extraction of the metals – nickel, iron, cobalt, copper – entails chemical processes such as smelting that poses environmental risks. In the mineral, arsenic is immobile and poses no environmental risk. Released from the mineral, arsenic is poisonous and mobile.
Zintl phases
[edit]
Partial reduction of arsenic with alkali metals (and related electropositive elements) affords polyarsenic compounds, which are members of the Zintl phases.
See also
[edit]- See Category:Arsenides for a list.
References
[edit]- ^ a b c d Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
- ^ Neupane, M.; Xu, S. Y.; Sankar, R.; Alidoust, N.; Bian, G.; Liu, C.; Belopolski, I.; Chang, T. R.; Jeng, H. T.; Lin, H.; Bansil, A.; Chou, F.; Hasan, M. Z. (2014). "Observation of a three-dimensional topological Dirac semimetal phase in high-mobility Cd3As2". Nature Communications. 5: 3786. arXiv:1309.7892. Bibcode:2014NatCo...5.3786N. doi:10.1038/ncomms4786. PMID 24807399. S2CID 32847905.
- ^ Liu, Z. K.; Jiang, J.; Zhou, B.; Wang, Z. J.; Zhang, Y.; Weng, H. M.; Prabhakaran, D.; Mo, S. K.; Peng, H.; Dudin, P.; Kim, T.; Hoesch, M.; Fang, Z.; Dai, X.; Shen, Z. X.; Feng, D. L.; Hussain, Z.; Chen, Y. L. (2014). "A stable three-dimensional topological Dirac semimetal Cd3As2". Nature Materials. 13 (7): 677–81. Bibcode:2014NatMa..13..677L. doi:10.1038/nmat3990. PMID 24859642.
- ^ Trukhan, V. M.; Izotov, A. D.; Shoukavaya, T. V. (2014). "Compounds and solid solutions of the Zn-Cd-P-As system in semiconductor electronics". Inorganic Materials. 50 (9): 868–873. doi:10.1134/S0020168514090143. S2CID 94409384.
- ^ He, Hua; Tyson, C.-T.; Bobev, S. (2011). "New compounds with (As7)3− Clusters: Synthesis and Crystal Structures of the Zintl Phases Cs2NaAs7, Cs4ZnAs14 and Cs4CdAs14". Crystals. 1 (3): 87–p98. doi:10.3390/cryst1030087.