Ultrafast Photoinduced Electron Transfer between an Incarcerated Donor and a Free Acceptor in Aqueous Solution

被引:51
|
作者
Porel, Mintu [2 ]
Chuang, Chi-Hung [1 ]
Burda, Clemens [1 ]
Ramamurthy, Vaidhyanathan [2 ]
机构
[1] Case Western Reserve Univ, Dept Chem, Cleveland, OH 44106 USA
[2] Univ Miami, Dept Chem, Coral Gables, FL 33124 USA
基金
美国国家科学基金会;
关键词
SOLVATION DYNAMICS; METHYL VIOLOGEN; ASSEMBLIES; WATER;
D O I
10.1021/ja3067594
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Supramolecular photoinduced electron transfer dynamics between coumarin 153 (C153) and 4,4'-dimethyl viologen dichloride (MV2+) across the molecular barrier of a host molecule, octa acid (OA), has been investigated with femtosecond time resolution. The ultrafast electron transfer from C153 to MV2+ followed excitation with 150 fs laser pulses at a wavelength of 390 nm despite the fact that C153 was incarcerated within an OA(2) capsule. As a result, the photoexcited coumarin did not show any of the typical relaxation dynamics that is usually observed in free solution. Instead, the excited electron was transferred across the molecular wall of the capsuleplex within 20 ps. Likewise, the lifetime of the charge transfer state was short (724 ps), and electron back-transfer reestablished the ground state of the system within 1 ns, showing strong electronic coupling among the excited electron donor, host, and acceptor. When the donor was encapsulated into the host molecule, the electron transfer process showed significantly accelerated dynamics and essentially no solvent relaxation compared with that in free solution. The study was also extended to N-methylpyridinium iodide as the acceptor with similar results.
引用
收藏
页码:14718 / 14721
页数:4
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