Mononuclear, helical binuclear palladium and lithium complexes bearing a new pyrrole-based NNN-pincer ligand: fluxional property.

A new pyrrole based NNN-pincer ligand, 2,5-bis(3,5-dimethylpyrazolylmethyl)pyrrole 2, was readily synthesized in two steps from pyrrole in 56% yield. The lithiation of the pincer ligand 2 using n-BuLi led to isolation of the dimeric lithium complex, [Li{μ-C(4)H(2)N-2,5-(CH(2)Me(2)pz)(2)-N,N,N}](2) 4, in 23% crystalline yield. The transmetalation reaction of 4 with [Pd(PhCN)(2)Cl(2)] afforded the mononuclear Pd(II) complex, [PdCl{C(4)H(2)N-2,5-(CH(2)Me(2)pz)(2)-N,N,N}] 5, containing one chloride ion in 45% yield. Alternatively 5 was obtained in an excellent yield of 87% by the reaction 2 of with [Pd(COD)Cl(2)] in the presence of triethylamine. On the contrary, a 20-membered macrometalacyclic molecule, [Pd(2)Cl(4){μ-C(4)H(3)N-2,5-(CH(2)Me(2)pz)(2)-N,N}(2)] 6, in which two PdCl(2) units are bridged by two molecules of 2 to give a helical structure, was synthesized by the reaction of 2 with [Pd(COD)Cl(2)] in the absence of base. The acetate analogue of complex 5, [Pd(OAc){C(4)H(2)N-2,5-(CH(2)Me(2)pz)(2)-N,N,N}] 3, was obtained by the treatment of 2 with [Pd(OAc)(2)]. The pyrrole twist angle of 5 is higher than that of 3. Complexes 3 and 5 show an AB pattern for their methylene protons at room temperature in CDCl(3) as well as in DMSO-d(6). The variable temperature NMR studies showed that the acetate and chloride complexes exhibit slightly different coalescence temperatures, which is a solvent dependent phenomenon, and twist angles.