Literature DB >> 28387515

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

Ashish Pandey1, Divya Dhingra1, Siddharth Pandey1.   

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.

Entities:  

Year:  2017        PMID: 28387515     DOI: 10.1021/acs.jpcb.7b01724

Source DB:  PubMed          Journal:  J Phys Chem B        ISSN: 1520-5207            Impact factor:   2.991


  6 in total

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Journal:  Front Chem       Date:  2022-05-09       Impact factor: 5.545

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Authors:  Suha Elderderi; Laura Wils; Charlotte Leman-Loubière; Sandra Henry; Hugh J Byrne; Igor Chourpa; Emilie Munnier; Abdalla A Elbashir; Leslie Boudesocque-Delaye; Franck Bonnier
Journal:  Anal Bioanal Chem       Date:  2021-06-01       Impact factor: 4.142

4.  A promising TNT alternative 3,3'-bi(1,2,4-oxadiazole)-5,5'-diylbis(methylene)dinitrate (BOM): thermal behaviors and eutectic characteristics.

Authors:  Xiong Yang; Jing Zhou; Xiaoling Xing; Yafeng Huang; Zhengfeng Yan; Qi Xue; Xiaofeng Wang; Bozhou Wang
Journal:  RSC Adv       Date:  2020-07-14       Impact factor: 4.036

5.  Deep eutectic solvent-catalyzed arylation of benzoxazoles with aromatic aldehydes.

Authors:  Phuong Hoang Tran; Anh-Hung Thi Hang
Journal:  RSC Adv       Date:  2018-03-20       Impact factor: 4.036

6.  In vitro toxicity assessment and enhanced drug solubility profile of green deep eutectic solvent derivatives (DESDs) combined with theoretical validation.

Authors:  Anil Kumar Jangir; Bhoomi Lad; Unnati Dani; Nehal Shah; Ketan Kuperkar
Journal:  RSC Adv       Date:  2020-06-24       Impact factor: 4.036

  6 in total

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