Functionalisable N-Heterocyclic Carbene-Triazole Palladium Complexes and Their Application in the Suzuki-Miyaura Reaction

Seven functionalised N‐heterocyclic carbene (NHC) ligands and their corresponding palladium(II) complexes have been synthesised with a triazole moiety as a modular and stable linkage between the catalytic centre and the secondary functional group. The complexes were prepared in good yields and fully...

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Veröffentlicht in:European journal of inorganic chemistry 2014-04, Vol.2014 (12), p.2088-2094
Hauptverfasser: Gogolieva, Ganna, Bonin, Hélène, Durand, Jérôme, Dechy-Cabaret, Odile, Gras, Emmanuel
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Sprache:eng
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Zusammenfassung:Seven functionalised N‐heterocyclic carbene (NHC) ligands and their corresponding palladium(II) complexes have been synthesised with a triazole moiety as a modular and stable linkage between the catalytic centre and the secondary functional group. The complexes were prepared in good yields and fully characterised by NMR spectroscopy, mass spectrometry and X‐ray crystallography. The complexes are active in the Suzuki–Miyaura cross‐coupling reaction, with catalytic activities maintained whatever the triazolyl substituent. This opens the possibility for various functionalisations of NHC–palladium complexes. New functionalised N‐heterocyclic carbene ligands and their corresponding palladium(II) complexes have been synthesised and fully characterised. The use of a triazole moiety as a modular and stable linkage between the catalytic centre and a targeted functionalisation does not damage the catalytic activity.
ISSN:1434-1948
1099-0682
DOI:10.1002/ejic.201301607