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Solid–state synthesis of polyhedral oligomeric silsesquioxane-supported N-heterocyclic carbenes/imidazolium salts on palladium nanoparticles: highly active and recyclable catalyst

Version 2 2024-06-13, 10:17
Version 1 2016-12-01, 15:27
journal contribution
posted on 2024-06-13, 10:17 authored by S Mohapatra, T Chaiprasert, R Sodkhomkhum, R Kunthom, S Hanprasit, P Santrirutnugul, V Ervithayasuporn
We describe a novel and green synthetic methodology for the fabrication of polyhedral oligomeric silsesquioxane-supported N-heterocyclic carbenes/imidazolium salts on palladium(II) complexes; Pd(II)-MPIm-POSS (1) composite by solid-state annealing between Pd(OAc)2 and octakis(3-(1-methylimidazolium)propyl) octasilsesquioxane without added base. Subsequently, arylboronic acid based in situ or ex situ reduction of 1 in aqueous ethanol produces polyhedral oligomeric silsesquioxane-supported N-heterocyclic carbenes/imidazolium salts on palladium nanoparticles; Pd(0)-nano-POSS (2) composite, consisting of monodispersed and N-heterocyclic carbene (NHC) stabilized Pd nanoparticles of very small size (3.0 ± 1.5 nm). Nanocatalyst 2 is a highly efficient and easily recyclable homogeneous catalyst for Suzuki-Miyaura cross-coupling reactions with TOF up to 1670 h−1.

History

Journal

Chemistry select

Volume

1

Pagination

5353-5357

Location

Weinheim, Germany

eISSN

2365-6549

Language

eng

Publication classification

C Journal article, C1.1 Refereed article in a scholarly journal

Copyright notice

2016, Wiley-VCH

Issue

16

Publisher

Wiley-VCH