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Iminophosphine palladium(II) complexes: synthesis, characterization, and application in Heck cross-coupling reaction of aryl bromides
Palladium(II) complexes containing phosphorus and nitrogen donor atoms (iminophosphine), dichlorido{N‐[2‐(diphenylphosphino)benzylidene]‐2‐trifluoromethylaniline}palladium(II) 1, dichlorido{N‐[2‐(diphenylphosphino)benzylidene]‐3‐trifluoromethylaniline}palladium(II) 2, dichlorido{N‐[2‐(diphenylphosph...
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Published in: | Applied organometallic chemistry 2014-07, Vol.28 (7), p.529-536 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Palladium(II) complexes containing phosphorus and nitrogen donor atoms (iminophosphine), dichlorido{N‐[2‐(diphenylphosphino)benzylidene]‐2‐trifluoromethylaniline}palladium(II) 1, dichlorido{N‐[2‐(diphenylphosphino)benzylidene]‐3‐trifluoromethylaniline}palladium(II) 2, dichlorido{N‐[2‐(diphenylphosphino)benzylidene]‐2‐methylaniline}palladium(II) 3, dichlorido{N‐[2‐(diphenylphosphino)benzylidene]‐3‐methylaniline}palladium(II) 4 have been successfully synthesized and fully characterized by FT‐IR and NMR (1H, 31P, 19F, and 13C) spectroscopy techniques. These complexes were first step tested in the reaction of bromobenzene and styrene to determine the optimal coupling reaction conditions and then successfully applied as catalysts for Heck cross‐coupling reactions of activated and deactivated aryl bromides with styrene derivatives and several acrylates. Copyright © 2014 John Wiley & Sons, Ltd.
Four iminophosphine ligands and their palladium(II) complexes were prepared and characterized. These hemilabile complexes were successfully applied as catalysts for Heck cross coupling reactions of activated and deactivated aryl bromides with styrene derivatives and several acrylates. |
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ISSN: | 0268-2605 1099-0739 |
DOI: | 10.1002/aoc.3158 |