Intersystem Crossing in Halogenated Bodipy Chromophores Used for Solar Hydrogen Production

被引:145
作者
Sabatini, Randy Pat [1 ]
McCormick, Theresa M. [1 ]
Lazarides, Theodore [1 ]
Wilson, Kristina C. [1 ]
Eisenberg, Richard [1 ]
McCamant, David W. [1 ]
机构
[1] Univ Rochester, Dept Chem, Rochester, NY 14627 USA
基金
加拿大自然科学与工程研究理事会;
关键词
CHARGE SEPARATION; DYE; ABSORPTION; CHEMISTRY;
D O I
10.1021/jz101697y
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
A series of halogenate boron-dipyrromethene (Bodipy) chromophores with potential applications in solar energy conversion were synthesized and characterized by steady state and ultrafast laser spectroscopy. The ultrafast dynamics of the chromophores were compared between a series containing H, Br, or I at the 2,6 positions of the Bodipy dye. The parent Bodipy has a fluorescent lifetime (tau(f1)) of 3-5 ns, a fluorescence quantum yield (P-q) of 0.56, and negligible triplet state yield. Bromination enhances the intersystem crossing (ISC) such that tau(n) and Phi(f1) decrease to similar to 1.2 ns and 0.11, respectively, while iodination further accelerates ISC so that tau(f1) is only similar to 130 ps and Phi(f1) is 0.011. Transient absorption experiments lead to the observation of excited state absorption bands from the singlet (S-1) and triplet (T-1) states at similar to 345 and 447 nm respectively and characterization of ISC via the dynamics of these bands and the decay of S-1 stimulated emission.
引用
收藏
页码:223 / 227
页数:5
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