期刊
GREEN CHEMISTRY
卷 10, 期 10, 页码 1055-1060出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/b805290e
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资金
- Vietnamese Government
- EPSRC [EP/D038162/1] Funding Source: UKRI
- Engineering and Physical Sciences Research Council [EP/D038162/1] Funding Source: researchfish
The Suzuki-Miyaura reaction has been performed using a non- symmetrical salen-type palladium(II) catalyst that is readily immobilized onto Merrifield resin and functionalized silica. The catalysts combine high activity with the recoverability and reusability offered by a heterogeneous system, without the need for phosphine ligands or additives. The high content of water used in the reaction, which is more than 96% by volume, represents a green process that should have advantages for industrial applications. Leaching of the metal into solution from the supported catalyst proved to be negligible.
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