首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Intramolecular charge transfer and solvation dynamics of coumarin 152 in aerosol-OT, water-solubilizing reverse micelles, and polar organic solvent solubilizing reverse micelles
【24h】

Intramolecular charge transfer and solvation dynamics of coumarin 152 in aerosol-OT, water-solubilizing reverse micelles, and polar organic solvent solubilizing reverse micelles

机译:香豆素152在气溶胶-OT,水溶性反胶束和极性有机溶剂反胶束中的分子内电荷转移和溶剂化动力学

获取原文
获取原文并翻译 | 示例
           

摘要

The relative retardation of intramolecular charge transfer (ICT) and the solvation dynamics of coumarin 152 in pure AOT, water, methanol, acetonitrile, and formamide reverse micelles have been investigated using picosecond time-resolved emission spectroscopy. The rate of ICT has been retarded almost 7 times at w(0) = 4 and 4 times at w(0) = 32 compared to that in pure water. The rate of retardation of ICT is also observed in the methanol and acetonitrile reverse micelles in comparison to that in pure methanol and acetonitrile. In pure AOT, the solvation time is 12.22 ns, but at w(0) = 4 of water reverse micelles the solvation. time is 7.27 ns. The slow dynamics in methanol, acetonitrile, and formamide reverse micelles is also observed. The relative retardation of the ICT rate is much smaller compared to the several thousand fold decrease in the solvation dynamics in the pool of the reverse micelles. The w dependency of solvation time is observed for water and methanol reverse micelles, but it is little for acetonitrile and none for formamide reverse micelles. The various w dependencies of solvation dynamics in water, methanol, and acetonitrile reverse micelles are explained on the basis of the presence, and the absence of hydrogen-bonding networks in water, methanol, and acetonitrile, respectively. [References: 45]
机译:使用皮秒时间分辨发射光谱法研究了纯AOT,水,甲醇,乙腈和甲酰胺反胶束中的分子内电荷转移(ICT)的相对延迟和香豆素152的溶剂化动力学。与纯水相比,ICT的速率在w(0)= 4时几乎降低了7倍,而在w(0)= 32时却降低了4倍。与纯甲醇和乙腈相比,在甲醇和乙腈反胶束中也观察到ICT的阻滞率。在纯AOT中,溶剂化时间为12.22 ns,但是在水的w(0)= 4处反胶束的溶剂化时间。时间是7.27 ns。还观察到甲醇,乙腈和甲酰胺反胶束中的缓慢动力学。与反胶束池中溶剂化动力学的下降几千倍相比,ICT速率的相对阻滞要小得多。对于水和甲醇反胶束,观察到溶剂化时间的w依赖性,但对于乙腈则几乎没有,而对于甲酰胺反胶束则没有。在水,甲醇和乙腈中分别存在和不存在氢键网络的基础上,解释了水,甲醇和乙腈反胶束中溶剂化动力学的各种依赖性。 [参考:45]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号