87825-62-5Relevant academic research and scientific papers
Reversible ligand pairing and sorting processes leading to Heteroligated Palladium(II) complexes with hemilabile ligands
Ulmann, Pirmin A.,Mirkin, Chad A.,DiPasquale, Antonio G.,Liable-Sands, Louise M.,Rheingold, Arnold L.
, p. 1068 - 1074 (2009/06/28)
Halide-induced ligand pairing and sorting processes have been observed in the context of Pd(II) complexes with hemilabile P,S and P,0 ligands. Mixing of the ligands Ph2PCH2CH2SMe (7) and Ph2PCH2CH2SPh (8) with a Pd(H) precursor in CH2C12 results in a mixture of [(7)2CIPd]CL [(8)2Cl2Pd], and [(7)(8)ClPd]Cl complexes at 20 °C. This equilibrium can be driven toward the heteroligated structure [(7)(8)ClPd]Cl by (1) cooling the mixture or (2) precipitation with hexanes, leading to the exclusive formation of semiopen heteroligated complex cis-[K2-(7)-K 1-(8)ClPd]Cl (9a), as confirmed by a single-crystal X-ray diffraction study and solid state CPMAS 31P1H} NMR spectroscopy. Dissolution of 9a in CH2C12 leads to the original mixture of complexes, which illustrates the reversible nature of this ligand pairing and sorting process. Similar processes occur when a combination of P,S and P,0 ligands is used. The semiopen heteroligated complexes can be chemically manipulated in a reversible fashion to form closed complexes, allowing for control of the relative position and flexibility between neighboring substituents in these "tweezer"-like structures. Control experiments suggest these ligand sorting and pairing processes occur via a halide-induced ligand rearrangement (HILR) reaction.
Complexes of platinum group metals with the ambidentate ligands Ph2P(CH2)nSPh (n=1, 2 )
Sanger, Alan R.
, p. 2214 - 2219 (2007/10/02)
The potencially bidentate ligands Ph2P(CH2)nSPh (n=1,2) form complexes of rhodium(I), iridium(I), palladium(II), or platinum(II) in which ligands are coordinated to a metal centre either by the phosphine function alone, or by the phosphine and the thioeth
