The relative anion-cation orientation in [(NHC) Au(alkene)] BF4 ion pairs [NHC _ N-Heterocyclic Carbene 1,3-bis(di-iso-propylphenyl)-imidazol-2-ylidene (IPr) and 4,5-dimethyl-N, N'-bis(2,6-diiso-propylphenyl)- imidazol-2-ylidene ((IPr)-I-Me); alkene 4-methyl-1-pentene, 2,3-methyl-2-butene and 4-methylstyrene] has been investigated by combining F-19, H-1-HOESY NMR spectroscopy in (CDCl2)-Cl-2 and a detailed analysis of the Coulomb potential of the cationic fragment through DFT calculations. Two main orientations have been found where the anion locates close to the imidazole ring (NHC-side) and close to the olefin (olefin-side). The NHC-side orientation is always predominant (65-83%) while the exact position of the anion in the olefin-side is finely tuned by the nature of olefin substituents. In all cases, the counterion resides far away from the gold site, the latter carrying only a small fraction of the positive charge. (C) 2010 Elsevier B.V. All rights reserved.

Ion pairing in NHC gold(I) olefin complexes: A combined experimental/theoretical study

ZUCCACCIA, Daniele;
2010-01-01

Abstract

The relative anion-cation orientation in [(NHC) Au(alkene)] BF4 ion pairs [NHC _ N-Heterocyclic Carbene 1,3-bis(di-iso-propylphenyl)-imidazol-2-ylidene (IPr) and 4,5-dimethyl-N, N'-bis(2,6-diiso-propylphenyl)- imidazol-2-ylidene ((IPr)-I-Me); alkene 4-methyl-1-pentene, 2,3-methyl-2-butene and 4-methylstyrene] has been investigated by combining F-19, H-1-HOESY NMR spectroscopy in (CDCl2)-Cl-2 and a detailed analysis of the Coulomb potential of the cationic fragment through DFT calculations. Two main orientations have been found where the anion locates close to the imidazole ring (NHC-side) and close to the olefin (olefin-side). The NHC-side orientation is always predominant (65-83%) while the exact position of the anion in the olefin-side is finely tuned by the nature of olefin substituents. In all cases, the counterion resides far away from the gold site, the latter carrying only a small fraction of the positive charge. (C) 2010 Elsevier B.V. All rights reserved.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11390/949758
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