Miswak mediated green synthesized palladium nanoparticles as effective catalysts for the Suzuki coupling reactions in aqueous media

Green and eco-friendly synthesis of palladium nanoparticles NPs is carried out under facile and eco-friendly conditions using an aqueous solution of Salvadora persica L. (SP) root extract (RE) as a bioreductant, which is commonly known as Miswak. The as-synthesized Pd NPs were characterized using va...

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Bibliographic Details
Published inJournal of Saudi Chemical Society Vol. 21; no. 4; pp. 450 - 457
Main Authors Khan, Mujeeb, Albalawi, Ghadeer H., Shaik, Mohammed Rafi, Khan, Merajuddin, Adil, Syed Farooq, Kuniyil, Mufsir, Alkhathlan, Hamad Z., Al-Warthan, Abdulrahman, Siddiqui, Mohammed Rafiq H.
Format Journal Article
LanguageEnglish
Published Riyadh, Saudi Arabia Elsevier B.V 01.05.2017
Saudi Chemical Society
Elsevier
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Summary:Green and eco-friendly synthesis of palladium nanoparticles NPs is carried out under facile and eco-friendly conditions using an aqueous solution of Salvadora persica L. (SP) root extract (RE) as a bioreductant, which is commonly known as Miswak. The as-synthesized Pd NPs were characterized using various spectroscopic and microscopic techniques, including, UV–Vis spectroscopy, FT-IR spectroscopy, XRD, ICP-MS and TEM. Detailed investigations of the Pd NPs have confirmed that the polyphenolic phytomolecules present in the RE of Miswak not only act as a bioreductant by facilitating the reduction and growth of Pd NPs, but they also functionalize the surface of Pd NPs and stabilized them in various solvents. Furthermore, the catalytic activity of the green synthesized Pd NPs was also tested toward the Suzuki coupling reactions of various aryl halides in aqueous media. The as-prepared Pd NPs exhibited superior catalytic activity and reusability for the Suzuki coupling reaction in aqueous and aerobic conditions. The kinetics of the reaction studied by GC revealed that the conversion of various aryl halides to biphenyl takes place in a short time.
ISSN:1319-6103
DOI:10.1016/j.jscs.2016.03.008