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解析不同链长的 1-烷基-3-甲基咪唑六氟磷酸盐离子液体的非均相微观黏度。

Unraveling heterogeneous microviscosities of the 1-alkyl-3-methylimidazolium hexafluorophosphate ionic liquids with different chain lengths.

机构信息

The State Key Laboratory of Molecular Reaction Dynamics, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China.

出版信息

Phys Chem Chem Phys. 2013 Oct 14;15(38):16074-81. doi: 10.1039/c3cp52724g. Epub 2013 Aug 27.

DOI:10.1039/c3cp52724g
PMID:23979295
Abstract

The rotational dynamics of coumarin 153 (C153) have been investigated in a series of 1-alkyl-3-methylimidazolium hexafluorophosphate ionic liquids with different alkyl chain lengths (alkyl = butyl, pentyl, hexyl, heptyl, octyl) ([Cnmim][PF6], n = 4-8) to examine the alkyl chain length dependent local viscosity of the microenvironment surrounding the probe molecules. The excimer-to-monomer fluorescence emission intensity ratio (IE/IM) of a well-known microviscosity probe, 1,3-bis(1-pyrenyl)propane (BPP), is also employed to study the microviscosity of [Cnmim][PF6] as a complementary measurement. The rotational dynamics of C153 show that at a certain length of the alkyl chain there are incompact and compact domains within [Cnmim][PF6], resulting in fast and slow components of C153 rotational dynamics. The microviscosities in different structural domains of [Cnmim][PF6] with different alkyl chain lengths are investigated by studying the fluorescence anisotropy decay of probe molecules. The obtained average rotation time constants show that with an increase in the length of the alkyl chain, the microviscosity of [Cnmim][PF6] is obviously increased first and then slightly decreased. The steady state fluorescence measurements with the microviscosity probe of BPP further prove that the microviscosity is not increased as much as expected when ionic liquids [Cnmim][PF6] have a relatively long alkyl chain. The different heterogeneous structures of [Cnmim][PF6] with different lengths of the alkyl chain are proposed to interpret the unusual microviscosity behaviors.

摘要

已在一系列具有不同烷基链长度的 1-烷基-3-甲基咪唑六氟磷酸盐离子液体([Cnmim][PF6],n = 4-8)中研究了香豆素 153(C153)的旋转动力学,以考察围绕探针分子的微环境中烷基链长度依赖性局部粘度。还使用众所周知的微粘度探针 1,3-双(1-芘基)丙烷(BPP)的荧光发射强度比(IE/IM)来研究[Cnmim][PF6]的微粘度,作为补充测量。C153 的旋转动力学表明,在烷基链的某个长度上,[Cnmim][PF6] 中存在不紧密和紧密的区域,导致 C153 旋转动力学的快和慢成分。通过研究探针分子的荧光各向异性衰减,研究了不同烷基链长度的[Cnmim][PF6]不同结构域中的微粘度。所得平均旋转时间常数表明,随着烷基链长度的增加,[Cnmim][PF6]的微粘度首先明显增加,然后略有降低。使用 BPP 微粘度探针的稳态荧光测量进一步证明,当离子液体[Cnmim][PF6]具有相对较长的烷基链时,微粘度的增加并不如预期的那样多。提出了具有不同烷基链长度的[Cnmim][PF6]的不同非均相结构来解释异常的微粘度行为。

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引用本文的文献

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