Versatile Palladium-catalyzed intramolecular cyclization to access new luminescent azaphosphaphenalene motifs.

Chemistry

Department of Green Chemistry and Technology, Synthesis, Bioresources and Bioorganic Chemistry Research Group, Ghent University, Coupure Links 653, 9000, Ghent, Belgium.

Published: April 2024

Using a straightforward sequence of diphosphonylation and a Pd-catalysed concerted-metalation-deprotonation (CMD), a synthetic strategy towards polyaromatic phosphorus containing heterocycles was developed. Herein, we report the synthesis and characterization of new azaphosphaphenalenes, using easily accessible palladium catalysts and starting materials. The key tetrahydroquinoline intermediates of the reaction were synthesised via a fast and effective procedure and could be isolated as such, or further reacted towards the target polyaromatic structures. The obtained products showed interesting luminescent properties and their emission, excitation and quantum yields were evaluated.

Download full-text PDF

Source
http://dx.doi.org/10.1002/chem.202303072DOI Listing

Publication Analysis

Top Keywords

versatile palladium-catalyzed
4
palladium-catalyzed intramolecular
4
intramolecular cyclization
4
cyclization access
4
access luminescent
4
luminescent azaphosphaphenalene
4
azaphosphaphenalene motifs
4
motifs straightforward
4
straightforward sequence
4
sequence diphosphonylation
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!