Ultrafast photoinduced electron transfer in the micelle and the gel phase of a PEO-PPO-PEO triblock copolymer

被引:27
|
作者
Mandal, Ujjwal [1 ]
Ghosh, Subhadip [1 ]
Dey, Shantanu [1 ]
Adhikari, Aniruddha [1 ]
Bhattacharyya, Kankan [1 ]
机构
[1] Indian Assoc Cultivat Sci Jadavpur, Dept Chem Phys, Kolkata 700032, India
来源
JOURNAL OF CHEMICAL PHYSICS | 2008年 / 128卷 / 16期
关键词
D O I
10.1063/1.2888553
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
Ultrafast photoinduced electron transfer (PET) from N,N-dimethylaniline (DMA) to coumarin dyes is studied in the micelle and the gel phase of a triblock copolymer, (PEO)(20)-(PPO)(70)-(PEO)(20) (Pluronic P123) by picosecond and femtosecond emission spectroscopies. The rate of PET in a P123 micelle and gel is found to be nonexponential and faster than the slow components of solvation dynamics. In a P123 micelle and gel, PET occurs on multiple time scales ranging from a subpicosecond time scale to a few nanoseconds. In the gel phase, the highest rate constant (9.3x10(9) M-1 s(-1)) of ET for C152 is about two times higher than that (3.8x10(9) M-1 s(-1)) observed in micelle phase. The ultrafast components of electron transfer (ET) exhibits a bell shaped dependence with the free energy change which is similar to the Marcus inversion. Possible reasons for slower PET in P123 micelle compared to other micelles and relative to P123 gel are discussed. (c) 2008 American Institute of Physics.
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页数:10
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