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溶剂控制的 1-丁基-3-甲基咪唑四氟硼酸盐和乙腈混合物中的分子内电子转移。

Solvent controlled intramolecular electron transfer in mixtures of 1-butyl-3-methylimidizolium tetrafluoroborate and acetonitrile.

机构信息

Department of Chemistry, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.

出版信息

J Chem Phys. 2018 May 21;148(19):193801. doi: 10.1063/1.5000727.

Abstract

Time-resolved emission techniques were used to study the excited-state intramolecular electron transfer of 9-(4-biphenyl)-10-methylacridinium (BPAc) in mixtures of 1-butyl-3-methylimidizolium tetrafluoroborate ([Im][BF])+ acetonitrile (ACN), a mixture previously shown to be of nearly constant polarity and nearly ideal mixing behavior. Reaction times ( ) track solvation times ( ) as a function of mixture composition over a range of more than 3 orders of magnitude in . This same correlation extends to a variety of neat dipolar solvents and ionic liquids. Reaction times are ∼2-fold larger than over most of the range studied but appear to reach a limiting value of ∼3 ps in the fastest solvents.

摘要

时间分辨发射技术被用于研究 9-(4-联苯基)-10-甲基吖啶鎓(BPAc)在 1-丁基-3-甲基咪唑四氟硼酸盐([Im][BF])+乙腈(ACN)混合物中的激发态分子内电子转移,该混合物先前被证明具有几乎恒定的极性和几乎理想的混合行为。反应时间()作为混合物组成的函数,在 范围内跟踪溶剂化时间(),范围超过 3 个数量级。这种相关性同样适用于各种纯偶极溶剂和离子液体。在研究的大部分范围内,反应时间比 大约大 2 倍,但在最快的溶剂中似乎达到了约 3 ps 的限制值。

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