Synthesis of palladium complexes derived from amido linked N-heterocyclic carbenes and their use in Suzuki cross coupling reactions
Abstract
Treatment of 1-(n-butyl)-3-N-(2-Ar)acetamido-1, 3-imidazolium chloride (Ar=furylmethyl,phenylmethyl) with excess K2CO3 and [PdCl2(L−L)] (L−L=2 PPh3, dppf) afforded orange compounds of composition [(1-(n-butyl)-3-N-(2-Ar)acetamido-1,3-imidazol-2-ylidene)]2Pd (Ar=furylmethyl; phenylmethyl). These complexes were characterized by NMR (1H and 13C{1H} NMR), IR and micro-analysis data. Subsequently, the catalytic efficiency of these complexes for cross coupling reactions between 4-haloarenens (halo=Br, I) and phenylboronic acid was studied under different solvents (acetonitrile, THF and DMF), temperatures with different catalyst loadings. The molecular structure of [(1-(n-butyl)-3-N-(2-furylmethyl)acetamido-1, 3-imidazol-2-ylidene)]2Pd was established by single crystal X-ray diffraction analysis.
Citation
Chauhan , R S , Nagar , S , Chatterjee , S , Goswami , D , Cordes , D B , Slawin , A M Z & Tawde , T 2021 , ' Synthesis of palladium complexes derived from amido linked N-heterocyclic carbenes and their use in Suzuki cross coupling reactions ' , Zeitschrift für Anorganische und Allgemeine Chemie , vol. Early View , pp. 1334-1341 . https://doi.org/10.1002/zaac.202100150
Publication
Zeitschrift für Anorganische und Allgemeine Chemie
Status
Peer reviewed
ISSN
0044-2313Type
Journal article
Rights
Copyright © 2021 Wiley-VCH GmbH. This work has been made available online in accordance with publisher policies or with permission. Permission for further reuse of this content should be sought from the publisher or the rights holder. This is the author created accepted manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at https://doi.org/10.1002/zaac.202100150
Description
One of the authors (RSC) is grateful to DST for the financial support under the DST young scientist scheme YSS/2014/000797.Collections
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