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区域选择性氘代钌(II)多吡啶配合物的共振拉曼光谱和寿命研究

Resonance Raman and lifetime studies on regioselectively deuteriated ruthenium(II) polypyridyl complexes.

作者信息

Browne Wesley R, Henry William, Passaniti Paolo, Gandolfi Maria Teresa, Ballardini Roberto, O'Connor Christine M, Brady Clare, Coates Colin G, Vos Johannes G, McGarvey John J

机构信息

National Centre for Sensor Research, School of Chemical Sciences, Dublin City University, Dublin 9, Ireland.

出版信息

Photochem Photobiol Sci. 2007 Apr;6(4):386-96. doi: 10.1039/b613471h. Epub 2007 Feb 9.

Abstract

Two series of ruthenium(II) polypyridyl complexes Ru(bipy)(2)(phpytr) and Ru(bipy)(2)(phpztr) (where Hphpytr = 2-(5-phenyl-1H-[1,2,4]triazol-3-yl)-pyridine and Hphpztr = 2-(5-phenyl-1H-[1,2,4]triazol-3-yl)-pyrazine) are examined by electrochemistry, UV/Vis, emission, resonance Raman, transient resonance Raman and transient absorption spectroscopy, in order to obtain a more comprehensive understanding of their excited state electronic properties. The interpretation of the results obtained is facilitated by the availability of several isotopologues of each of the complexes examined. For the pyridine-1,2,4-triazolato based complex the lowest emissive excited state is exclusively bipy based, however, for the pyrazine based complexes excited state localisation on particular ligands shows considerable solvent and pH dependency.

摘要

通过电化学、紫外/可见光谱、发射光谱、共振拉曼光谱、瞬态共振拉曼光谱和瞬态吸收光谱对两组钌(II)多吡啶配合物[Ru(bipy)(2)(phpytr)]⁺和[Ru(bipy)(2)(phpztr)]⁺(其中Hphpytr = 2-(5-苯基-1H-[1,2,4]三唑-3-基)-吡啶,Hphpztr = 2-(5-苯基-1H-[1,2,4]三唑-3-基)-吡嗪)进行了研究,以便更全面地了解它们的激发态电子性质。所研究的每种配合物的几种同位素异构体的存在有助于对所得结果进行解释。对于基于吡啶-1,2,4-三唑的配合物,最低发射激发态仅基于联吡啶,然而,对于基于吡嗪的配合物,激发态在特定配体上的定位显示出相当大的溶剂和pH依赖性。

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