Abstract
A new polymer-anchored Pd(II) complex has been synthesized, characterized and its catalytic activity was investigated for the Suzuki cross-coupling reaction between aryl halides and arylboronic acid in the presence of K2CO3 as a base, for Heck olefination of aryl halides with alkenes, and for cyanation reaction of aryl iodides with K4Fe(CN)6 in presence of Et3N as base. The key features of the catalyst include rapid reactions with excellent conversion without the use of phosphine ligands and total stability under the reactions conditions. The catalyst was recovered by simple filtration and reused five-times without significant loss of catalytic activity.
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Acknowledgements
We thank the Indian Association for the Cultivation of Science for providing the instrumental support. We acknowledge the Department of Science and Technology (DST), Council of Scientific and Industrial Research (CSIR) and the University Grant Commission (UGC), New Delhi, India for funding. We also thank the DST and UGC, New Delhi, India for providing instrumental support under the FIST and SAP program.
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Islam, S.M., Mondal, P., Tuhina, K. et al. A Reusable Polymer-Anchored Palladium(II) Schiff Base Complex Catalyst for the Suzuki Cross-Coupling, Heck and Cyanation Reactions. J Inorg Organomet Polym 20, 264–277 (2010). https://doi.org/10.1007/s10904-010-9352-y
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DOI: https://doi.org/10.1007/s10904-010-9352-y