A series of novel complexes [Ni(η5-C5H 4R)(L)(NHC)]+A-2a-2j and [Ni(η5- C5H5)(A)(NHC)] 3a-3c has been obtained by anion metathesis from the corresponding chlorides 1a-1d, depending on the anion binding properties and reaction conditions. Solid-state structures of two cationic complexes (2c, 2j) and two complexes with a coordinated anion (3a, 3c) have been determined by X-ray diffraction revealing a trigonal planar geometry in all cases. Unexpectedly, 3c displayed unprecedented for this type of compounds temperature-dependent NMR spectra that were interpreted in terms of spin equilibrium. The cationic complexes 2 were less efficient in styrene polymerization than the parent chlorides 1. However, the activity of 2 and 3 in Suzuki cross-coupling did not depend considerably on the counterion. © 2014 the Partner Organisations.
CITATION STYLE
Buchowicz, W., Banach, Ł., Conder, J., Guńka, P. A., Kubicki, D., & Buchalski, P. (2014). Anion exchange in [Ni(η5-C5H4R)(Cl) (NHC)]. Counterion effect on the structure and catalytic activity. Dalton Transactions, 43(15), 5847–5857. https://doi.org/10.1039/c3dt53352b
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