Chakrabarty Debdeep, Seth Debabrata, Chakraborty Anjan, Sarkar Nilmoni
Department of Chemistry, Indian Institute of Technology, Kharagpur, West Bengal 721302, India.
J Phys Chem B. 2005 Mar 31;109(12):5753-8. doi: 10.1021/jp045715t.
The effects of confinement of the ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate on solvation dynamics and rotational relaxation of Coumarin 153 (C-153) in Triton X-100/cyclohexane microemulsions have been explored using steady-state and picosecond time-resolved emission spectroscopy. The steady-state and rotational relaxation data indicate that C-153 molecules are incorporated in the core of the microemulsions. The average rotational relaxation time increases with increase in w ([bmim][BF(4)]/[TX-100]) values. The solvent relaxation in the core of the microemulsion occurs on two different time scales and is almost insensitive to the increase in w values. The solvent relaxation is retarded in the pool of the microemulsions compared to the neat solvent. Though, the retardation is very small compared to several-fold retardation of the solvation time of the conventional solvent inside the pool of the microemulsions.
利用稳态和皮秒时间分辨发射光谱,研究了离子液体1-丁基-3-甲基咪唑四氟硼酸盐的受限作用对香豆素153(C-153)在Triton X-100/环己烷微乳液中的溶剂化动力学和旋转弛豫的影响。稳态和旋转弛豫数据表明,C-153分子被纳入微乳液的核中。平均旋转弛豫时间随w([bmim][BF₄]/[TX-100])值的增加而增加。微乳液核中的溶剂弛豫发生在两个不同的时间尺度上,并且对w值的增加几乎不敏感。与纯溶剂相比,微乳液池中溶剂弛豫受到阻碍。不过,与微乳液池中常规溶剂的溶剂化时间几倍的延迟相比,这种延迟非常小。