Difference between revisions of "Delocalized electron"

Jump to: navigation, search
m (1 revision(s))
m (Robot: Automated text replacement (-(?ms)^(.*)$ +\1 {{WikiDoc Sources}}))
Line 25: Line 25:
 
[[zh:離域電子]]
 
[[zh:離域電子]]
 
[[fi:Delokalisaatio]]
 
[[fi:Delokalisaatio]]
 +
{{WikiDoc Sources}}

Revision as of 02:21, 25 May 2008

Template:Unref

Benzene, with the delocalization of the electrons indicated by the circle.

In chemistry delocalized electrons are electrons in a molecule that are not associated with a single atom or to a covalent bond. Delocalized electrons are contained within an orbital that extends over several adjacent atoms. Classically, delocalized electrons can be found in conjugated systems of double bonds and in aromatic and mesoionic systems. A case of delocalized electrons occurs also in solid metals, where the d-subshell interferes with the above s-subshell, and contributes to the properties of a metal. It is increasingly appreciated that electrons in sigma bonding levels are also delocalized. For example, in methane, the bonding electrons are shared by all five atoms equally. Pervasive existence of delocalization is implicit in Molecular Orbital Theory.

In the simple aromatic ring of benzene the delocalization of six π electrons over the C6 ring is often graphically indicated by a circle. The fact that the six C-C bonds are equidistant is one indication of this delocalization. In Valence Bond Theory, delocalization in benzene is represented by resonance structures.

Another example of a delocalized electrons can be found in a carboxylate group, wherein the negative charge is centered equally on the two oxygen atoms.

Delocalized electrons are important for several reasons. One, an expected chemical reaction may not occur because the electrons delocalize to a more stable configuration, resulting in a reaction that happens at a different location. An example attempting the Fridel-Crafts alkylation of benzene with 1-chloro-2-methylpropane; the carbocation rearranges to a tert-butyl group stabilized by hyperconjugation, a particular form of delocalization.

Delocalized electrons also exist in the structure of metals. Metallic structure consist of aligned positive ions (cations) in a "sea" of delocalized electrons. This means that the electrons are free to move throughout the structure, and gives rise to properties such as conductivity.

In diamond all four outer electrons of each carbon atom are 'localized' between the atoms in covalent bonding. The movement of electrons is restricted and diamond does not conduct an electric current. In graphite, each carbon atom uses only 3 of its 4 outer energy level electrons in covalently bonding to three other carbon atoms in a plane. Each carbon atom contributes one electron to a delocalized system of electrons that is also a part of the chemical bonding. The delocalized electrons are free to move throughout the plane. For this reason, graphite conducts electricity along the planes of carbon atoms, but does not conduct in a direction at right angles to the plane.

ar:إلكترون غير متمركز de:Delokalisierung it:Elettrone delocalizzato nl:Gedelokaliseerd elektron sv:Delokaliserad elektron fi:Delokalisaatio


Linked-in.jpg