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5,11-Conjugation-extended low-bandgap anthradithiophene-containing polymer exhibiting enhanced thin-film order and

Ying Jiang1, Jianguo Mei, Alexander L Ayzner

  • 1Department of Chemical Engineering, Stanford University, Stanford, CA 94305-5025, USA.

Chemical Communications (Cambridge, England)
|June 16, 2012
PubMed

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The Diels–Alder reaction is an example of a thermal pericyclic reaction between a conjugated diene and an alkene or alkyne, commonly referred to as a dienophile. The reaction involves a concerted movement of six π electrons, four from the diene and two from the dienophile, forming an unsaturated six-membered ring. As a result, these reactions are classified as [4+2] cycloadditions.