Synthesis and properties in solution of rodlike, 2,2 ': 6 ',2 ''-terpyridine-based ruthenium(II) coordination polymers

Rodlike ruthenium(II) coordination polymers have been prepared via the conv ersion of 4,4 "-bis(2,2':6',2 "-terpyridine)-2',5'-dihexyl-p-terphenyl and an appropriately reactive ruthenium(III) species in 1-butanol/DMA. The diam agnetic polymers readily dissolve in polar organic solvents, and their homo geneous constitution could thus be proven and their degrees of polycondensa tion could be estimated to be P-n greater than or equal to 30, using H-1 an d C-13 NMR spectroscopy. The Pd-catalyzed polycondensation of bis[4'-(p-bro mophenyl)-2,2':6',2 "-terpyridine]ruthenium(II) tetrafluoroborate and 2,5-d ihexylbenzene-1,4-diboronic acid, on the other hand, which should lead to a constitutionally identical polymer, only resulted in oligomers under all t ested conditions. The intrinsic viscosity [eta] of the high-molecular-weigh t polymers (determined in 0.02 M NH4PF6/DMA) is of the order of 300 mL g(-1 ). In salt-free DMA solution and thus at low ionic strengths, the polymers display the characteristic polyelectrolyte behavior in viscosity experiment s which becomes more and more pronounced with increasing P-n. The UV-vis ab sorption spectra re corded in DMA solution do not show any evidence of intr amolecular electronic interactions of the metal centers along the polymer c hains: on the contrary, the coordination polymers behave like sequences of electronically independent ruthenium(II) complexes.