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氢键供体/受体共溶剂改性的基于氯化胆碱的低共熔溶剂

Hydrogen Bond Donor/Acceptor Cosolvent-Modified Choline Chloride-Based Deep Eutectic Solvents.

作者信息

Pandey Ashish, Dhingra Divya, Pandey Siddharth

机构信息

Department of Chemistry, Indian Institute of Technology Delhi , Hauz Khas, New Delhi 110016, India.

出版信息

J Phys Chem B. 2017 Apr 27;121(16):4202-4212. doi: 10.1021/acs.jpcb.7b01724. Epub 2017 Apr 7.

Abstract

Deep eutectic solvents (DESs) have emerged as nontoxic and inexpensive alternatives not only to the common organic solvents but to the ionic liquids as well. Some of the common and popular, and perhaps the most investigated, DESs are the ones comprising an ammonium salt and an appropriate hydrogen bond (HB) donor in a predetermined mole ratio. The formation of the DES is attributed to the H-bonding interaction(s) present between the salt and the HB donor. Consequently, addition of a predominantly HB donor or a predominantly HB acceptor cosolvent to such DESs may result in intriguing features and properties. We present investigation of two DESs constituted of salt choline chloride along with HB donors urea and glycerol, respectively, in 1:2 mol ratio, named reline and glyceline as the cosolvent of very high HB donating acidity and no HB accepting basicity 2,2,2-trifluoroethanol (TFE) and of very high HB accepting basicity and no HB donating acidity hexamethylphosphoramide (HMPA), respectively, is added. TFE shows up to 0.25 mole fraction miscibility with both reline and glyceline. While up to 0.25 mole fraction HMPA in glyceline results in transparent mixtures, this cosolvent is found to be completely immiscible with reline. From the perspective of the solvatochromic absorbance and fluorescence probes, it is established that the cybotactic region dipolarity within up to 0.25 mole fraction TFE/HMPA-added DES strongly depends on the functionalities present on the solute. Fourier transform infrared absorbance and Raman spectroscopic investigations reveal no major shifts in vibrational transitions as TFE/HMPA is added to the DES; spectral band broadening, albeit small, is observed nonetheless. Excess molar volumes and excess logarithmic viscosities of the mixtures indicate that while TFE may interstitially accommodate itself within H-bonded network of reline, it does appear to form H-bonds with the constituents of the glyceline. Increase in overall net repulsive interactions as HMPA is added to glyceline is suggested by both positive excess molar volumes and excess logarithmic viscosities. The addition of HB donor/acceptor cosolvent appears to disturb the salt-HB donor equilibria within DES via complex interplay of interactions within the system.

摘要

深共熔溶剂(DESs)已成为无毒且廉价的替代品,不仅可替代常见的有机溶剂,还可替代离子液体。一些常见且受欢迎,或许也是研究最多的DESs是由铵盐和适当的氢键(HB)供体按预定摩尔比组成的。DES的形成归因于盐与HB供体之间存在的氢键相互作用。因此,向此类DES中添加主要为HB供体或主要为HB受体的共溶剂可能会产生引人入胜的特性。我们分别研究了两种由氯化胆碱盐与HB供体尿素和甘油按1:2摩尔比构成的DES,分别命名为relone和glyceline,作为具有非常高的HB供体酸度且无HB受体碱性的2,2,2 - 三氟乙醇(TFE)以及具有非常高的HB受体碱性且无HB供体酸度的六甲基磷酰胺(HMPA)的共溶剂添加进去。TFE与relone和glyceline的互溶度高达0.25摩尔分数。虽然在glyceline中加入高达0.25摩尔分数的HMPA会得到透明混合物,但发现这种共溶剂与relone完全不互溶。从溶剂化显色吸收和荧光探针的角度来看,已确定在添加高达0.25摩尔分数TFE/HMPA的DES中,近程有序区域偶极矩强烈依赖于溶质上存在的官能团。傅里叶变换红外吸收和拉曼光谱研究表明,当向DES中添加TFE/HMPA时,振动跃迁没有重大位移;尽管观察到的光谱带展宽很小,但仍有展宽。混合物的过量摩尔体积和过量对数粘度表明,虽然TFE可能会间隙性地容纳在relone的氢键网络中,但它似乎确实与glyceline的成分形成了氢键。正的过量摩尔体积和过量对数粘度都表明,当向glyceline中添加HMPA时,整体净排斥相互作用增加。添加HB供体/受体共溶剂似乎通过系统内相互作用的复杂相互作用扰乱了DES内的盐 - HB供体平衡。

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