Ab Initio Investigation of the Interionic Interactions in Triethylammonium-Based Protic Ionic Liquids: The Role of Anions in the Formation of Ion Pair and Hydrogen Bonded Structure

2018 ◽  
Vol 123 (1) ◽  
pp. 293-300 ◽  
Author(s):  
Irina V. Fedorova ◽  
Lyubov P. Safonova

2021 ◽  
Vol 23 (4) ◽  
pp. 2663-2675
Author(s):  
Viviane Overbeck ◽  
Henning Schröder ◽  
Anne-Marie Bonsa ◽  
Klaus Neymeyr ◽  
Ralf Ludwig

NMR Fast-Field-Cycling (FFC) relaxometry provides important information about translational and rotational dynamics of hydrogen bonded protic ionic liquids (PILs). 



2021 ◽  
Author(s):  
Daniel B. Werz ◽  
Ivan A. Andreev ◽  
Nina K. Ratmanova ◽  
André U. Augustin ◽  
Olga A. Ivanova ◽  
...  


Langmuir ◽  
2018 ◽  
Vol 34 (44) ◽  
pp. 13449-13458 ◽  
Author(s):  
Zhongyang Dai ◽  
Lili Shi ◽  
Linghong Lu ◽  
Yunhao Sun ◽  
Xiaohua Lu




2009 ◽  
Vol 11 (39) ◽  
pp. 8790 ◽  
Author(s):  
Koichi Fumino ◽  
Alexander Wulf ◽  
Ralf Ludwig


2012 ◽  
Vol 65 (11) ◽  
pp. 1502 ◽  
Author(s):  
Natalie Debeljuh ◽  
Swapna Varghese ◽  
Colin J. Barrow ◽  
Nolene Byrne

We report on the impact of changes in the protic ionic liquid (pIL) cation on the fibrilisation kinetics and the conversion of the Aβ 16–22 from monomers to amyloid fibrils. When we compare the use of primary, secondary, and tertiary amines we find that the primary amine results in the greatest conversion into amyloid fibrils. We show that the pIL is directly interacting with the peptide and this likely drives the difference in conversion and kinetics observed.



2008 ◽  
Vol 47 (16) ◽  
pp. 7121-7132 ◽  
Author(s):  
Svetlana Begel ◽  
Peter Illner ◽  
Simon Kern ◽  
Ralph Puchta ◽  
Rudi van Eldik


2007 ◽  
Vol 111 (35) ◽  
pp. 8717-8723 ◽  
Author(s):  
Henrik Markusson ◽  
Jean-Philippe Belières ◽  
Patrik Johansson ◽  
C. Austen Angell ◽  
Per Jacobsson


2016 ◽  
Vol 18 (40) ◽  
pp. 27745-27749 ◽  
Author(s):  
Aditi Bhattacherjee ◽  
Sanjay Wategaonkar

Hydrogen-bonded water bridges are re-directed from a polar NH bond to a weakly activated C(2)–H bond upon N-methylation. Infrared spectra, supported by ab initio calculations, provide direct evidence of the role of the C(2)–H donor in the solvation of the imidazole ring.



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