TY  - JOUR
AU  - De León, A.
AU  - Ayllón, J.A.
AU  - Pons, J.
T1  - Tuning the hemilabile behaviour of a thioetherepyrazole ligand on Pd(II) complexes with diphosphines
LA  - eng
PY  - 2012
SP  - 4275
EP  - 4280
T2  - Journal of Organometallic Chemistry
SN  - 0022-328X
VL  - 696
IS  - 26
PB  - Elsevier B.V.
AB  - 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.
DO  - 10.1016/j.jorganchem.2011.10.003
UR  - https://portalciencia.ull.es/documentos/619e21030f42206e37be2999
DP  - Dialnet - Portal de la Investigación
ER  -