Elucidating the Quenching Mechanism of Tris(2,2′-bipyridyl)ruthenium(II) Complex in the Water-Glycerol Binary System Based on the Microscopic Structure of the Media

被引:1
|
作者
Hamano, Yuki [1 ]
Inagawa, Arinori [1 ]
Otsuka, Takuhiro [2 ]
Kageyama, Ryo [1 ]
Ogawa, Juri [1 ]
Roppongi, Makoto [3 ]
Higashiguchi, Takeshi [1 ]
Uehara, Nobuo [1 ]
机构
[1] Utsunomiya Univ, Fac Engn, Utsunomiya 3218585, Japan
[2] Tokyo Inst Technol, Dept Chem, Tokyo 1528551, Japan
[3] Utsunomiya Univ, Ctr Instrumental Anal, Utsunomiya 3218585, Japan
基金
日本学术振兴会;
关键词
ELECTRON-TRANSFER REACTIONS; TEMPERATURE-DEPENDENCE; EXCITED RU(BPY)3(2+); PHASE COEXISTENT; SOLVATION; RUTHENIUM(II); HYDRATION; LIQUID; FLUORESCENCE; ACID;
D O I
10.1021/acs.jpcb.3c07882
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Kinetic studies on the photochemical quenching reaction of the tris(2,2'-bipyridyl) ruthenium(II) complex ([Ru(bpy)(3)](2+)) in water-glycerol binary media were conducted based on the Einstein-Smoluchowski (E-S) theory. Dynamic and static quenching behaviors were analyzed by comparing results from time-resolved spectroscopy and emission spectroscopy. While the dynamic quenching reaction aligns well with the E-S theory, static quenching was observed, leading to a notable increase in the overall photoquenching reaction rate constant. Employing chromatography and infrared spectroscopy, we correlated the microscopic molecular structure of the binary solvent system and the solvation environment around the emitters with the reaction mechanism. This correlation was found to correspond to ion pair formation and the confinement effect of the emitter, respectively.
引用
收藏
页码:1771 / 1779
页数:9
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