Reliable and short synthetic routes to polycyclic aromatic hydrocarbons and nanographenes are important in materials science. Herein, we report an efficient one-step annulative π-extension reaction of alkynes that provides access to diarylphenanthrenes and related nanographene precursors. In the presence of a cationic palladium/o-chloranil catalyst system and dibenzosiloles or dibenzogermoles as π-extending agents, a variety of diarylacetylenes are transformed successfully into 9,10-diarylphenanthrenes in a single step with good functional-group tolerance. Furthermore, double π-extension reactions of 1,4-bis(phenylethynyl)benzene and diphenyl-1,3-butadiyne are demonstrated, affording oligoarylene products, which show potential for application in the synthesis of larger polycyclic aromatic hydrocarbons and nanographenes.

Download full-text PDF

Source
http://dx.doi.org/10.1002/anie.201610374DOI Listing

Publication Analysis

Top Keywords

one-step annulative
8
annulative π-extension
8
dibenzosiloles dibenzogermoles
8
polycyclic aromatic
8
aromatic hydrocarbons
8
hydrocarbons nanographenes
8
π-extension alkynes
4
alkynes dibenzosiloles
4
dibenzogermoles palladium/o-chloranil
4
palladium/o-chloranil catalysis
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!