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A highly active and recyclable homogeneous NHC–palladium catalyst with pH- and light-sensitive tags for the Suzuki–Miyaura coupling reactions of aryl halides with arylboronic acids†
Guiyan Liu,Chengxin Liu,Xia Zhao,Jianhui Wang
RSC Advances Pub Date : 04/29/2016 00:00:00 , DOI:10.1039/C6RA08272F
Abstract

The design and synthesis of a stable, highly active, and recyclable homogeneous palladium catalyst for Suzuki–Miyaura coupling reactions is of great interest. A well-defined N-heterocyclic carbene (NHC) Pd(II) complex with pH- and light-sensitive nitrobenzospiropyran (SP) tags has been synthesized in good yields via a series of simple steps. This complex is a homogeneous catalyst which has excellent reactivities for the Suzuki–Miyaura coupling of aryl bromides and aryl chlorides with arylboronic acids. Significantly, at a low loading (0.2 mol%), this catalyst has very good recyclability in an i-PrOH–H2O solvent system (1 : 1 v/v), under mild conditions. By making use of the pH- and light-sensitive SP tags, the catalyst can be recovered and reused seven times.

Graphical abstract: A highly active and recyclable homogeneous NHC–palladium catalyst with pH- and light-sensitive tags for the Suzuki–Miyaura coupling reactions of aryl halides with arylboronic acids
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