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Abstract
This paper reports an environmentally friendly and highly efficient synthesis of organic semiconductor materials via a Pd/N‐heterocyclic carbene (NHC)‐catalyzed Suzuki reaction in aqueous ethanol with high isolated yields (86–98%). Firstly, four glucopyranoside‐substituted NHC precursors with poly(ethylene glycol) (PEG) chains were synthesized and characterized. The NHC precursor with the longest PEG chain (n = 16) was found to be the most efficient ligand in the reactions of a wide range of aryl halides and arylboronic acids. The best catalyst system obtained in this work could be recycled five times without significant loss of catalytic activity.l Copyright © 2016 John Wiley & Sons, Ltd.
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