Abstract
This contribution focuses on the coordination behaviour of 2-[2-(diphenylphosphino)phenyl]-1,3-diisopropylguanidine (1), which is a representative of the unique P,N-ligands combining phosphine moieties with strongly basic guanidinium substituents. This compound was prepared by the reaction of 2-(diphenylphosphino)aniline with 1,3-diisopropylcarbodiimide in the presence of diethylzinc (10 mol%).
When mixed with [MCl2L2] (M = Pd, Pt; L = a weakly bonding ligand), ligand 1 gives rise to P,N-chelate complexes [MCl2(1-κ(2) P,N)]. However, in the case of kinetically inert Pt(II), the products of partial substitution and chloride ionisation, [PtCl(1-κ(2) P,N)(L)]Cl, where L = Me2SO or η(2)-cycloocta-1,5-diene, can be intercepted.
Ionisation also occurs in the reaction with [PdCl(η(3)-C3H5)]2, leading to [Pd(η(3)-C3H5)(1-κ(2) P,N)]Cl, while [Pd(MeCN)4][BF4]2 produces the bis-chelate complex, cis-[Pd(1-κ(2) P,N)2][BF4]2. In contrast, the corresponding hydrochloride (1H)Cl behaves as a simple phosphine, reacting with PdCl2 surrogates to give the zwitterionic species [PdCl3(1H-κP)] and the bis-phosphine complex trans-[PdCl2(1H-κP)2]Cl2, depending on the metal-to-ligand ratio.