Supramolecular Control of the Spin-Dependent Dynamics of Long-Lived Charge-Separated States at the Micellar Interface As Studied by Magnetic Field Effect

被引:6
|
作者
Miura, Tomoaki [1 ]
机构
[1] Keio Univ, Dept Chem, Fac Sci & Engn, Kohoku Ku, Yokohama, Kanagawa 2238522, Japan
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2013年 / 117卷 / 21期
关键词
PHOTOINDUCED ELECTRON-TRANSFER; RADICAL PAIR RECOMBINATION; TRITON X-100 MICELLE; TIME-RESOLVED EPR; TEMPERATURE-DEPENDENCE; AROMATIC-HYDROCARBONS; EXCIPLEX LUMINESCENCE; EXCHANGE INTERACTION; AGGREGATION NUMBER; MARCUS INVERSION;
D O I
10.1021/jp401725f
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
Spin selectivity in long-lived charge separation at the micellar interface is studied using the magnetic field effect (MFE). An amphiphilic viologen is complexed with a nonionic surfactant to form a supramolecular acceptor cage, of which the size is controlled by the acceptor concentration, as confirmed by dynamic light scattering measurement. Photoinduced electron transfer (ET) from a guest polyaromatic molecule to the viologen moiety is observed spin-dependently with time-resolved fluorescence (trFL) and transient absorption (TA). A negative MFE on the radical yield is successfully observed, which indicates generation of singlet-born long-lived radical pair that is realized by supramolecular control of the donor-acceptor (D-A) distances. The dominance of the singlet-precursor MFE is sensitive to the acceptor concentration, which presumably affects the D-A distance as well as the cage size. However, theoretical analysis of the MFE gives large recombination rates of ca. 10(8) s(-1), which indicate the contribution of spin-allowed recombination of the pseudocontact radical pair generated by still active in-cage diffusion. Dependence of the viologen concentration and alkyl chain length on the recombination and escape dynamics is discussed in terms of precursor spin states and the microenvironments in the cage.
引用
收藏
页码:6443 / 6454
页数:12
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