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Photochemically Induced Energy-Transfer Effects on the Decay Times of Ruthenium Complexes in Polymers

机译:光化学诱导的能量转移对聚合物中钌配合物衰变时间的影响

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摘要

The effects of photobleaching on absorption properties and decay limes of ruthenium complexes adsorbed on silica gel or dissolved in polystyrene or PVC are reported. While complexes with bipyridyl ligands adsorbed on silica gel did not show any decay time decrease at all, complexes having phenanthroline ligands exhibit a significant pho-todegradation which is manifested not only by a decrease in luminescence intensity but also by decay time decrease and specific absorption spectral changes. The effects are shown to depend strongly on the oxygen and dye concen-trations present at the bleaching process. The absorption bands of the photoproducts of ruthenium—phenanthroline complexes overlap with the emission spectra of the intact molecules. Flirster resonance energy transfer from intact ruthenium complexes to their own photoproducts, gener-ated by singlet oxygen attack of the phenanthroline bridges of the ligands, is suggested to be responsible for the observed decay time effects.
机译:据报道,光漂白对吸附在硅胶上或溶解在聚苯乙烯或PVC中的钌配合物的吸收性能和衰变石灰的影响。尽管具有吸附在硅胶上的联吡啶基配体的配合物根本没有显示任何衰减时间的减少,但是具有菲咯啉配体的配合物显示出显着的光降解,这不仅表现为发光强度的降低,还表现为衰减时间的减少和比吸收光谱的降低变化。结果表明,效果很大程度上取决于漂白过程中存在的氧气和染料浓度。钌-菲咯啉配合物的光产物的吸收带与完整分子的发射光谱重叠。从配体的菲咯啉桥的单线态氧攻击产生的从完整的钌络合物到它们自身的光产物的调光剂共振能量转移,是造成观察到的衰变时间效应的原因。

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