Abstract
The coordination mode of thioetherepyrazole ligand, 1,5-bis(3,5-dimethyl-1- pyrazolyl)-3-thiapentane (bdtp) and 1,8-bis-(3,5-dimethyl-1-pyrazolyl)-3,6- dithiaoctane (bddo) ligands, in Pd(II) complexes containing a diphosphine ligand is determined by subtle changes in size of the bridge between the two phosphorus atoms. The 1HNMRand 31P{1H}NMR at variable temperature in acetonitrile solutionprove that the hemilabile character of the bdtp ligand depend on the diphosphine ligand. Thus, while in [Pd(bdtp)(dppe)](BF4)2 [1](BF4)2 the thioether group not participate in the Pd(II) coordination sphere, two isomers with different coordination (P2N2 vs P2NS) are in equilibrium in [Pd(bdtp)(dppp)](BF4)2 [2](BF4)2 acetonitrile solution. For complexes [Pd(bddo)(dppe)](BF4) 2 [3](BF4)2 and [Pd(bddo)(dppp)](BF 4)2 [4](BF4)2, only the coordination N,N is observed. © 2011 Elsevier B.V. All rights reserved.
Original language | English |
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Pages (from-to) | 4275-4280 |
Journal | Journal of Organometallic Chemistry |
Volume | 696 |
Issue number | 26 |
DOIs | |
Publication status | Published - 1 Jan 2012 |
Keywords
- Diphosphine ligands
- Hemilabile ligand
- N,S ligands
- Palladium
- Pyrazole