Arsenide

{{Short description|Anion}} 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.<ref name="Greenwood" >{{Greenwood&Earnshaw}}</ref>

==Alkali metal and alkaline earth arsenides== 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&nbsp;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.<ref name="Greenwood"/> The compound LiAs, has a metallic lustre and electrical conductivity indicating some metallic bonding.<ref name="Greenwood"/> 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

thumb|220px|right|Nickel arsenide is a common impurity in ores of nickel. It is also a prototype of a class of structures.

==III–V compounds== {{main|List of semiconductor materials}} 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== {{main|:Category:II-V compounds}} 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.<ref>{{Cite journal | doi = 10.1038/ncomms4786| pmid = 24807399| title = Observation of a three-dimensional topological Dirac semimetal phase in high-mobility Cd₃As₂| 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 Cd₃As₂| 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> 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.<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>

==Polyarsenides== ===Transition metal arsenides=== Arsenic anionics are known to catenate, that is, form chains, rings, and cages. The mineral skutterudite (CoAs₃) 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 (PtAs₂) 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.

===Zintl phases=== [[File:423080Asonly.png|thumb|right|Structure of [As₇]³⁻ subunit in the Zintl phase Cs₂NaAs₇.<ref>{{cite journal|title=New compounds with (As₇)³⁻ Clusters: Synthesis and Crystal Structures of the Zintl Phases Cs₂NaAs₇, Cs₄ZnAs₁₄ and Cs₄CdAs₁₄|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>]] Partial reduction of arsenic with alkali metals (and related electropositive elements) affords polyarsenic compounds, which are members of the Zintl phases.

==See also== *See :Category:Arsenides for a list.

==References== {{Reflist}}

{{Arsenides}} {{Monatomic anion compounds}}

Category:Anions Category:Arsenides Category:Arsenic(−III) compounds