Cross-conjugation

From Wikipedia, the free encyclopedia
Jump to navigation Jump to search

Cross-conjugation is a special type of conjugation in a molecule, when in a set of three pi bonds only two pi bonds interact with each other by conjugation, while the third one is excluded from interaction.[1][2]

File:Cross Conjugation Triene V.1.svg

Whereas a normal conjugated system such as a polyene typically has alternating single and double bonds along consecutive atoms, a cross-conjugated system has an alkene unit bonded to one of the middle atoms of another conjugated chain through a single bond. In classical terms, one of the double-bonds branches off rather than continuing consecutively: the main chain is conjugated, and part of that same main chain is conjugated with the side group, but all parts are not conjugated together as strongly. Examples of cross-conjugation can be found in molecules such as benzophenone, Template:Chem name, p-quinones, dendralenes, radialenes, fullerene, and Indigo dye. The type of conjugation affects reactivity and molecular electronic transitions.

References

<templatestyles src="Reflist/styles.css" />

  1. IUPAC, Compendium of Chemical Terminology, 5th ed. (the "Gold Book") (2025). Online version: (2006–) "cross-conjugation". Script error: No such module "CS1 identifiers".Script error: No such module "TemplatePar".
  2. Script error: No such module "Citation/CS1".

Script error: No such module "Check for unknown parameters".