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'''Isoelectronicity''' is a [[phenomenon]] observed when two or more [[molecule]]s have the same [[chemical structure|structure]] (positions and connectivities among [[atom]]s) and the same [[electron configuration|electronic configuration]]s, but differ by what specific [[chemical element|elements]] are at certain locations in the structure. For example, {{chem|CO|link=carbon monoxide}}, {{chem|NO|+|link=nitrosonium}}, and {{chem|N|2|link=Nitrogen}} are isoelectronic, while {{chem|CH|3|CO|CH|3|link=acetone}} and {{chem|CH|3|N}}={{chem|N|CH|3|}} are not.<ref>{{GoldBookRef|title=isoelectronic|file=I03276}}</ref>   
'''Isoelectronicity''' is a [[phenomenon]] observed when two or more [[molecule]]s have the same [[chemical structure|structure]] (positions and connectivities among [[atom]]s) and the same [[electron configuration|electronic configuration]]s, but differ by what specific [[chemical element|elements]] are at certain locations in the structure. For example, {{chem|CO|link=carbon monoxide}}, {{chem|NO|+|link=nitrosonium}}, and {{chem|N|2|link=Nitrogen}} are isoelectronic, while {{chem|CH|3|CO|CH|3|link=acetone}} and [[Azomethane|CH<sub>3</sub>N=NCH<sub>3</sub>]] are not.<ref>{{GoldBookRef|title=isoelectronic|file=I03276}}</ref>   


This definition is sometimes termed '''valence isoelectronicity'''.  Definitions can sometimes be not as strict, sometimes requiring identity of the total [[electron]] count and with it the entire [[electron configuration|electronic configuration]].<ref>[http://www.iun.edu/~cpanhd/C101webnotes/chemical-bond/isoelectronic.html Isoelectronic Configurations] {{Webarchive|url=https://web.archive.org/web/20170717073429/http://www.iun.edu/~cpanhd/C101webnotes/chemical-bond/isoelectronic.html |date=2017-07-17 }} ''iun.edu''</ref>  More usually, definitions are broader, and may extend to allowing different numbers of atoms in the [[chemical species|species]] being compared.<ref>A. A. Aradi & T. P. Fehlner, "Isoelectronic Organometallic Molecules", in F. G. A. Stone & Robert West (eds.) ''Advances in Organometallic Chemistry Vol. 30'' (1990), Chapter 5 (at p. 190) [https://books.google.com/books?id=e6R4oMRDhvsC&pg=PA190 google books link]</ref>
This definition is sometimes termed '''valence isoelectronicity'''.  Definitions can sometimes be not as strict, sometimes requiring identity of the total [[electron]] count and with it the entire [[electron configuration|electronic configuration]].<ref>[http://www.iun.edu/~cpanhd/C101webnotes/chemical-bond/isoelectronic.html Isoelectronic Configurations] {{Webarchive|url=https://web.archive.org/web/20170717073429/http://www.iun.edu/~cpanhd/C101webnotes/chemical-bond/isoelectronic.html |date=2017-07-17 }} ''iun.edu''</ref>  More usually, definitions are broader, and may extend to allowing different numbers of atoms in the [[chemical species|species]] being compared.<ref>A. A. Aradi & T. P. Fehlner, "Isoelectronic Organometallic Molecules", in F. G. A. Stone & Robert West (eds.) ''Advances in Organometallic Chemistry Vol. 30'' (1990), Chapter 5 (at p. 190) [https://books.google.com/books?id=e6R4oMRDhvsC&pg=PA190 google books link]</ref>

Latest revision as of 01:18, 19 June 2025

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Isoelectronicity is a phenomenon observed when two or more molecules have the same structure (positions and connectivities among atoms) and the same electronic configurations, but differ by what specific elements are at certain locations in the structure. For example, Template:Chem, Template:Chem, and Template:Chem are isoelectronic, while Template:Chem and CH3N=NCH3 are not.[1]

This definition is sometimes termed valence isoelectronicity. Definitions can sometimes be not as strict, sometimes requiring identity of the total electron count and with it the entire electronic configuration.[2] More usually, definitions are broader, and may extend to allowing different numbers of atoms in the species being compared.[3]

The importance of the concept lies in identifying significantly related species, as pairs or series. Isoelectronic species can be expected to show useful consistency and predictability in their properties, so identifying a compound as isoelectronic with one already characterised offers clues to possible properties and reactions. Differences in properties such as electronegativity of the atoms in isolelectronic species can affect reactivity.

In quantum mechanics, hydrogen-like atoms are ions with only one electron such as Template:Chem. These ions would be described as being isoelectronic with hydrogen.

Examples

Template:Multiple image Template:Multiple image

The Template:Chem atom and the Template:Chem ion are isoelectronic because each has five valence electrons, or more accurately an electronic configuration of [He] 2s2 2p3.

Similarly, the cations Template:Chem, Template:Chem, and Template:Chem and the anions Template:Chem, Template:Chem, and Template:Chem are all isoelectronic with the Template:Chem atom.

Template:Chem, Template:Chem, Template:Chem, and Template:Chem are isoelectronic because each has two atoms triple bonded together, and due to the charge have analogous electronic configurations (Template:Chem is identical in electronic configuration to Template:Chem so Template:Chem is identical electronically to Template:Chem).

Molecular orbital diagrams best illustrate isoelectronicity in diatomic molecules, showing how atomic orbital mixing in isoelectronic species results in identical orbital combination, and thus also bonding.

More complex molecules can be polyatomic also. For example, the amino acids serine, cysteine, and selenocysteine are all isoelectronic to each other. They differ by which specific chalcogen is present at one location in the side-chain.

Template:Chem (acetone) and Template:Chem (azomethane) are not isoelectronic. They do have the same number of electrons but they do not have the same structure.

See also

References

Template:Reflist

  1. Template:GoldBookRef
  2. Isoelectronic Configurations Template:Webarchive iun.edu
  3. A. A. Aradi & T. P. Fehlner, "Isoelectronic Organometallic Molecules", in F. G. A. Stone & Robert West (eds.) Advances in Organometallic Chemistry Vol. 30 (1990), Chapter 5 (at p. 190) google books link