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

被引:164
作者
Kelch, S [1 ]
Rehahn, M [1 ]
机构
[1] Univ Karlsruhe, Inst Polymer, D-76128 Karlsruhe, Germany
关键词
D O I
10.1021/ma990266u
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Rodlike ruthenium(II) coordination polymers have been prepared via the conversion 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 diamagnetic polymers readily dissolve in polar organic solvents, and their homogeneous constitution could thus be proven and their degrees of polycondensation could be estimated to be P-n greater than or equal to 30, using H-1 and C-13 NMR spectroscopy. The Pd-catalyzed polycondensation of bis[4'-(p-bromophenyl)-2,2':6',2 "-terpyridine]ruthenium(II) tetrafluoroborate and 2,5-dihexylbenzene-1,4-diboronic acid, on the other hand, which should lead to a constitutionally identical polymer, only resulted in oligomers under all tested conditions. The intrinsic viscosity [eta] of the high-molecular-weight 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 experiments which becomes more and more pronounced with increasing P-n. The UV-vis absorption spectra re corded in DMA solution do not show any evidence of intramolecular electronic interactions of the metal centers along the polymer chains: on the contrary, the coordination polymers behave like sequences of electronically independent ruthenium(II) complexes.
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页码:5818 / 5828
页数:11
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