scholarly journals Imidazolium-based ionic liquids with large weakly coordinating anions

2017 ◽  
Vol 41 (4) ◽  
pp. 1677-1686 ◽  
Author(s):  
William Levason ◽  
David Pugh ◽  
Gillian Reid

An investigation into the intramolecular interactions in a series of imidazolium salts with weakly coordinating anions reveals that it is possible to control the strength and location of hydrogen bonding by varying the substituents on the imidazolium cation.

2011 ◽  
Vol 115 (49) ◽  
pp. 14688-14697 ◽  
Author(s):  
Ekaterina I. Izgorodina ◽  
Radha Maganti ◽  
Vanessa Armel ◽  
Pamela M. Dean ◽  
Jennifer M. Pringle ◽  
...  

2020 ◽  
Vol 235 (8-9) ◽  
pp. 365-374
Author(s):  
Kai Richter ◽  
Katharina V. Dorn ◽  
Volodymyr Smetana ◽  
Anja-Verena Mudring

AbstractA set of imidazolium-based ionic liquids (ILs), 1-(2-hydroxyethyl)-3-methylimidazolium chloride (1), 1,3-bis-(2-hydroxyethyl)-imidazolium chloride (2), and 1-butyl-2,3,4,5-tetramethylimidazolium bromide (3), has been synthesized and their structural and thermal behavior studied. Organic halides are well-known IL formers with imidazolium halides being the most prominent ones. Functionalization of the imidazolium cation by enhancing its hydrogen bonding capacity, i.e. through introduction of –OH groups or by diminishing it, i.e. through substitution of the ring hydrogen atoms by methyl groups is expected to change the inter-ionic interactions. Consequently, the solid-state structures of 1–3 have been characterized with means of single X-ray diffraction to shed light on preferential inter-ionic interactions for obtaining valuable information on anti-crystal engineering, i.e. designing ion combinations that favor a low melting point and exhibit a low tendency for crystallization. The study reveals that endowing IL forming ions with an enhanced hydrogen bonding capacity leads to a depression in melting points and kinetically hinders crystallization. This study provides hints towards new design concepts for IL design, similar to the common strategy of employing conformationally flexible ions.


2006 ◽  
Vol 632 (12-13) ◽  
pp. 2164-2164 ◽  
Author(s):  
Tudor Timofte ◽  
Anja-Verena Mudring

Author(s):  
Ahmed Elaiwi ◽  
Peter B. Hitchcock ◽  
Kenneth R. Seddon ◽  
Narmatha Srinivasan ◽  
Yu-May Tan ◽  
...  

2021 ◽  
Author(s):  
Firoz Shah Tuglak Khan ◽  
Amy L Waldbusser ◽  
Maria C. C. Carrasco ◽  
Hadi Pourhadi ◽  
Shabnam Hematian

A facile and effective strategy for the preparation of a series of ferricenium complexes bearing either electron-donating or electron-withdrawing substituents with weakly coordinating anions such as [B(C6F5)4]– or SbF6– is...


2021 ◽  
Vol 328 ◽  
pp. 115391
Author(s):  
Vinícius Castro Ferreira ◽  
Letícia Zanchet ◽  
Wesley Formentin Monteiro ◽  
Letícia Guerreiro da Trindade ◽  
Michèle Oberson de Souza ◽  
...  

Author(s):  
MingMin Zhong ◽  
Hong Fang ◽  
Deepika Deepika ◽  
Purusottam Jena

Stabilization of multiply-charged atomic clusters in the gas phase has been a topic of great interest not only because of their potential applications as weakly-coordinating anions, but also for their...


2015 ◽  
Vol 17 (46) ◽  
pp. 30978-30982 ◽  
Author(s):  
Anne Knorr ◽  
Koichi Fumino ◽  
Anne-Marie Bonsa ◽  
Ralf Ludwig

Spectroscopic evidence for cation–cation interaction in ionic liquids. The repulsive electrostatic interaction is overcome by hydrogen bonding between ions of like charge.


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