Pd-SILP-Fe3O4@SiO2: An efficient supported ionic liquid phase catalyst for the Mizoroki-Heck coupling

Suraj Ashok Sonawane; Dattaprasad Marutrao Pore

doi:10.30574/ijsra.2023.10.2.0902

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Pd-SILP-Fe3O4@SiO2: An efficient supported ionic liquid phase catalyst for the Mizoroki-Heck coupling

Suraj Ashok Sonawane ¹and Dattaprasad Marutrao Pore ^{2, *}

1 Department of Chemistry, Rajaram College Kolhapur, Maharashtra (INDIA) – 416004.
2 Department of Chemistry, Shivaji University, Kolhapur, Maharashtra (INDIA) – 416004.

Research Article

International Journal of Science and Research Archive, 2023, 10(02), 096–106.

Article DOI: 10.30574/ijsra.2023.10.2.0902

DOI url: https://doi.org/10.30574/ijsra.2023.10.2.0902

Publication history

Received on 04 October 2023; revised on 03 November 2023; accepted on 06 November 2023

Abstract

An efficient method for the Mizoroki-Heck coupling of aryl halides with alkenes employing already reported palladium tagged, magnetic nanoparticle supported, ionic liquid phase catalyst (Pd-SILP-Fe3O4@SiO2) in water under aerobic conditions has been developed. Various di-substituted alkenes were synthesized with excellent yields using a highly water dispersible Pd-SILP-Fe3O4@SiO2 catalyst. This nanocatalyst displayed high thermal stability, compatibility in aqueous systems, high catalytic efficiency, high turnover frequencies (TOF), easy magnetic recovery, and reusability up to 6th run. The main advantages of the protocol are its robustness, mild reaction conditions, easy set-up, easy workup, low Pd loading (0.001 mol% of Pd), higher yields, and use of water as a green solvent, which makes it both environmentally and economically appealing.

Keywords

Supported ionic liquid; Magnetic Nanoparticles; Mizoroki-Heck coupling; Reusability; Water dispersible catalyst; SILP

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How to cite this article

Suraj Ashok Sonawane and Dattaprasad Marutrao Pore. Pd-SILP-Fe3O4@SiO2: An efficient supported ionic liquid phase catalyst for the Mizoroki-Heck coupling. International Journal of Science and Research Archive, 2023, 10(02), 096–106. Article DOI: https://doi.org/10.30574/ijsra.2023.10.2.0902

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