[[Image:Diamond and graphite.jpg|thumb|300px|Diamond and graphite are two allotropes of carbon: pure forms of the same element that differ in structure.]]'''Allotropy''' (Gr. ''allos'', other, and ''tropos'', manner) is a behavior exhibited by certain [[chemical element]]s: these elements can exist in two or more different forms, known as ''allotropes'' of that element. In each different allotrope, the element's atoms are bonded together in a different manner.

For example, the element [[carbon]] has two common allotropes: [[diamond]], where the carbon atoms are bonded together in a [[tetrahedral]] lattice arrangement, and [[graphite]], where the carbon atoms are bonded together in sheets of a hexagonal lattice.

Note that allotropy refers only to different forms of an element within the same phase or [[state of matter]] (i.e. different [[solid]], [[liquid]] or [[gas]] forms) - the changes of state between solid, liquid and gas in themselves
are not considered allotropy. For some elements, allotropes have different molecular formulae which can persist in different phases - for example, the two allotropes of [[oxygen]] ([[dioxygen]], O<sub>2</sub> and [[ozone]], O<sub>3</sub>), can both exist in the solid, liquid and gaseous states. Conversely, some elements do not maintain distinct allotropes in different phases: for example [[phosphorus]] has numerous solid allotropes, which all revert to the same P<sub>4</sub> form when melted to the liquid state.

== History ==
The concept of allotropy was originally proposed in 1841 by the Swedish scientist Baron [[Jons Jakob Berzelius]] (1779-1848) who offered no explanation.<ref>Jensen W.B., "The Origin of the Term Allotrope", Journal of Chemical Education, 2006, '''83''', 838-9 </ref> After the acceptance of [[Avogadro]]'s hypothesis in 1860 it was understood that elements could exist as polyatomic molecules, and the two allotropes of oxygen were recognized as O<sub>2</sub> and O<sub>3</sub>. In the early 20th century it was recognized that other cases such as carbon were due to differences in crystal structure.

By 1912, [[Wilhelm Ostwald|Ostwald]] noted that the allotropy of elements is just a special case of the phenomenon of
[[Polymorphism (materials science)|polymorphism]] known for compounds, and proposed that the terms allotrope and allotropy be abandoned and replaced by polymorph and polymorphism. Although many other chemists have repeated this advice, [[IUPAC]] and most chemistry texts still favour the usage of allotrope and allotropy for elements only.

== Differences in properties of an element's allotropes ==
Allotropes
are different structural forms of the same element and can exhibit quite different physical properties and chemical behaviours. The change between allotropic forms is triggered by the same forces that affect other structures, i.e. [[pressure]], [[photochemistry|light]], and [[temperature]]. Therefore the stability of the particular allotropes depends on particular conditions. For instance, [[iron]] changes from a [[body-centered cubic]] structure [[Ferrite (iron)|(ferrite)]] to a [[face-centered cubic]] structure ([[austenite]]) above 906 °C, and [[tin]] undergoes a transformation known as [[tin pest]] from a [[metallic]] phase to a [[semiconductor]] phase below 13.2 °C.

== Examples of allotropes
==
{{Expand|date=December 2007}}
Typically, elements capable of variable [[coordination number]] and/or [[oxidation states]] tend to exhibit greater numbers of allotropic forms. Another contributing factor is the ability of an element to [[catenation|catenate]]. Allotropes are typically more noticeable in [[non-metal]]s and [[metalloid]]s.

Examples of allotropes include:

''[[Carbon]]'':
{{main|Allotropes of carbon}}
* [[diamond]] - an extremely hard, transparent crystal, with the carbon atoms arranged in a tetrahedral lattice. A poor
electrical conductor. An excellent thermal conductor.
* [[graphite]] - a soft, black, flaky solid, a moderate electrical conductor. The C atoms are bonded in flat hexagonal lattices, which are then layered in sheets.
* [[fullerene]] - (including the "buckyball", C<sub>60</sub>)

''[[Phosphorus
]]'':
{{main|Allotropes of phosphorus}}
* Red phosphorus - polymeric solid
* White
phosphorus - crystalline solid
* Black
phosphorus - semiconductor, analogous to graphite

''[[Oxygen
]]'':
{{main|Allotropes of oxygen}}
* [[dioxygen]], O<sub>2</sub> - colorless
*[[ozone]], O<sub>3</sub> - blue
*[[tetraoxygen]], O<sub>4</sub> - red

''[[Sulfur
]]'':
{{main|Allotropes of sulfur}}
*Plastic (amorphous) sulfur - polymeric solid
*Rhombic sulfur - large crystals composed of S<sub>8</sub> molecules

<!--*Monoclinic sulfur - fine needle-like crystals-->
*Other
ring molecules such as S<sub>7</sub> and S<sub>12</sub>

Selenium:
*"Red selenium," cyclo-Se<sub>8</sub>
*Gray selenium, polymeric Se

Arsenic:
*Yellow arsenic, As<sub>4</sub>
*Gray arsenic, polymeric As

''[[Plutonium]]'' has six distinct solid allotropes under "normal" pressures. Their densities vary within a ratio of some 4:3, which vastly complicates all kinds of work with the metal (particularly casting, machining, and storage). A seventh plutonium allotrope exists at very high pressures, which adds further difficulties in exotic applications.

==External links==

*Allotrope in ''IUPAC Compendium of Chemical Terminology'', Electronic version, http://goldbook.iupac.org/A00243.html. Accessed March 2007
.

==References==
<references/>


[[Category:Allotropy]]
[[Category:Inorganic chemistry]]

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