Dynamic self-assembly of an M3L6 molecular triangle and an M4L8 tetrahedron from naked PdII ions and bis(3-pyridyl)-substituted arenes

The pyridine-appended nonchelating bidentate ligands 1,4-bis(3-pyridyl)benzene (1) and 4,4'-bis(3-pyridyl) biphenyl (2) were complexed with a naked Pd-II ion for the construction of molecular cage compounds. Prior to these experiments, the complexation of the ligands with cis-[Pd(en)(NO3)(2)] was also examined, because self-assemblies from the cis-protected Pd-II ion were expected to be simple motifs that constitute the assemblies from naked Pd-II ion. The structures of the self-assembled compounds resulting from 1 and [Pd(en)(NO3)(2)] depended on the solvent employed. In aqueous solution, an M2L2 trenchlike compound was obtained. In dimethyl sulfoxide, however, a mixture of the M2L2 trench and an M3L3 macrocycle was found in equilibrium, the dynamic nature of which was confirmed by the concentration-dependent nature of the species. At higher concentration, an M4L4 macrocycle was mostly observed. The complexation of 1 with naked Pd-II ions was expected to produce novel structures that are combinations of the MnLn type frameworks. A peculiar tetrahedral M4L8 assembly was obtained quantitatively from 1 and Pd(NO3)(2), rather than the smallest possible M3L6 double-walled triangle. In terestingly, the use of Pd(CF3SO3)(2) resulted in the sole formation of the latter structure. Thus, the anion is important as a template in the formation of these assemblies. Ligand 2, which contains an extra p-phenylene unit compared to 1, behaved in a similar manner when treated with [Pd(en)(NO3)(2)], but showed subtle differences with naked Pd-II ions. With Pd(NO3)(2), 2 gave mostly a tetrahedron along with a double-walled triangle. With Pd(CF3SO3)(2), this longer ligand formed a double-walled triangle with a negligible amount of tetrahedra. A single discrete assembly of a perfect tetrahedron was obtained from 2 and Pd-II ions by choosing p-tosylate as a counterion.