Paul Aniruddha, Mandal Prasun Kumar, Samanta Anunay
School of Chemistry, University of Hyderabad, Hyderabad 500 046, India.
J Phys Chem B. 2005 May 12;109(18):9148-53. doi: 10.1021/jp0503967.
Room-temperature ionic liquids, particularly those based on substituted imidazolium cations, are currently being extensively studied for a variety of applications. Herein, we explore the suitability of several imidazolium salts in optical applications by carefully examining the electronic absorption and fluorescence behavior of these substances, generally believed to be transparent in most of the UV region and fully transparent in the visible region. It is shown that all imidazolium ionic liquids are characterized by significant absorption in the entire UV region and a long absorption tail that extends into the visible region. These absorption characteristics are attributed to the imidazolium moiety and its various associated structures. When excited in the UV or early part of the visible region, these liquids exhibit fluorescence, which covers a large part of the visible region and shows dramatic excitation wavelength dependence. The excitation wavelength dependent shift of the fluorescence maximum has been rationalized taking into consideration the existence of the various associated structures of the ionic liquids and the inefficiency of the excitation energy-transfer process between them. The results imply that these liquids may have serious drawbacks in some of the optical studies.
室温离子液体,特别是那些基于取代咪唑阳离子的离子液体,目前正因其各种应用而受到广泛研究。在此,我们通过仔细研究这些物质的电子吸收和荧光行为,探索了几种咪唑盐在光学应用中的适用性,这些物质通常被认为在大部分紫外区域是透明的,在可见光区域是完全透明的。结果表明,所有咪唑离子液体的特征是在整个紫外区域有显著吸收,并且有一个长吸收尾延伸到可见光区域。这些吸收特性归因于咪唑部分及其各种相关结构。当在紫外或可见光区域的早期激发时,这些液体表现出荧光,其覆盖了可见光区域的大部分,并表现出显著的激发波长依赖性。考虑到离子液体各种相关结构的存在以及它们之间激发能量转移过程的低效性,荧光最大值的激发波长依赖性位移已得到合理解释。结果表明,这些液体在某些光学研究中可能存在严重缺陷。