Long-range photoinduced electron transfer dynamics in rigid media

被引:10
|
作者
Ito, Akitaka [1 ,2 ]
Fang, Zhen [1 ]
Brennaman, M. Kyle [1 ]
Meyer, Thomas J. [1 ]
机构
[1] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
[2] Osaka City Univ, Grad Sch Sci, Dept Chem, Sumiyoshi Ku, Osaka 5588585, Japan
关键词
TRANSFER RATE CONSTANTS; MLCT EXCITED-STATES; ENERGY-TRANSFER; CHARGE-TRANSFER; PHOTOPHYSICAL PROPERTIES; RUTHENIUM(II) COMPLEXES; INTERVALENCE TRANSFER; DISTANCE DEPENDENCE; TRANSFER ABSORPTION; ORGANIC GLASSES;
D O I
10.1039/c3cp54801e
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
In semi-rigid PEG-DMA550 films with added reductive quenchers, electron transfer quenching of the metalto- ligand charge transfer excited state(s) of [Ru(bpy)(3)](2+) (bpy = 2,2'-bipyridine) occurs by both rapid, fixedsite, and slow, diffusional, quenching processes. Stern-Volmer analysis of diffusional quenching reveals diffusion-controlled quenching both in the fluid and film with the latter greatly inhibited by the high viscosity of the medium. The data for fixed-site quenching are consistent with electron tunneling with the expected exponential distance dependence. Based on this analysis long-range electron transfer occurs with a distance attenuation factor beta' of similar to 0.47 (A) over circle (-1) with a notable decrease, beta = 0.16 (A) over circle (-1), when the quencher is incorporated into the PEG backbone. Fixed-site electron transfer quenching varies with driving force. Back electron transfer is complex, as expected for a distribution of fixed sites, and varies with power law kinetics.
引用
收藏
页码:4880 / 4891
页数:12
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