Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, Department of Chemistry, Shandong University, Jinan 250100, China.
J Colloid Interface Sci. 2011 Jan 15;353(2):476-81. doi: 10.1016/j.jcis.2010.09.069. Epub 2010 Sep 29.
A perylenetetracarboxylic diimide (PDI) compound with an attached hydrophilic polyoxyethylene group at the imide nitrogen position was designed and synthesized. Photoinduced electron and energy transfer between coumarin 153 (C-153) and PDI in a ternary microemulsion with an ionic liquid (bmimPF(6)/TX-100/H(2)O) were investigated by steady state electronic absorption and fluorescence spectroscopy. The results revealed that both PDI and C-153 resided at the interface between the surfactant TX-100 and the ionic liquid bmimPF(6) in the ternary microemulsions. The absorption spectra suggested no interactions between C-153 and PDI in the ground states, but the fluorescence spectra revealed the presence of an efficient electron transfer and a less efficient energy transfer from C-153 to PDI. Moreover, the electron transfer was much more efficient in microemulsions than that in homogeneous conventional organic solvents due to the unique micro-environment of the microemulsion.
设计并合成了一种在酰亚胺氮位连接有亲水性聚氧乙烯基团的苝四羧酸二酰亚胺(PDI)化合物。通过稳态电子吸收和荧光光谱研究了在离子液体(bmimPF(6)/TX-100/H(2)O)的三元微乳液中香豆素 153(C-153)与 PDI 之间的光诱导电子和能量转移。结果表明,在三元微乳液中,PDI 和 C-153 都位于表面活性剂 TX-100 和离子液体 bmimPF(6)之间的界面处。吸收光谱表明 C-153 和 PDI 在基态之间没有相互作用,但荧光光谱表明 C-153 向 PDI 发生了有效的电子转移和效率较低的能量转移。此外,由于微乳液的独特微环境,电子转移在微乳液中比在均相传统有机溶剂中更加高效。