Hydrogen Bonding (H‐bonds) between ions of like charge challenges the fundamental principle of electrostatics that opposite charges attract and like charges repel. This study provides direct structural and spectroscopic evidence of H‐bonded anionic wires in protic ionic liquids (PILs), which consist of triethylammonium cations and hydrogen dicarboxylate anions. The anionic wires were identified by X‐ray crystallography in the solid state, wherein the anions are linked by −OH···O− type H‐bonds. The H‐bonds within the anionic wire are significantly stronger than those between cation and anion despite repulsive Coulomb interaction in the first and attractive ones in the latter case. Analysis by nuclear magnetic resonance (NMR) and infrared (IR) spectroscopy suggests that the binding motifs of the solid structure are mainly preserved in the liquid state of the supercooled PILs. This conclusion is drawn from density functional theory (DFT) calculations of the same structural motifs as observed in the solid state. The calculated 1H NMR chemical shifts and IR C═O frequencies for these H‐bond structures correspond well with the measured spectroscopic signatures. The anionic chains remain intact even when gradually removing the counterions. Our findings highlight the fundamental role of hydrogen bonding for the unusual attractive interaction between ions of like charge.
The structural and electronic properties of 1:1 complexes of tetrabutylammonium bromide (TBAB) with oxalic, adipic, succinic, and citric acids were investigated using density functional theory (DFT) at the B3LYP‐D3/6‐311++G(d,p) level. The molecular electrostatic potential surface analysis was employed to identify...
A. Kazachenko, U. Holikulov, O. Fetisova et al.· ChemistrySelect· 0 citations
Structures of mono cationic di cationic and tri cationic ionic liquids [M]
+
, [D]
++
, and [T]
+++
with halide anions (X) where X = Cl¯, Br¯, and I¯ were studied using density functional theory (DFT). The most stable geometry of this structures were computed and compared with others. In di‐cationic ionic liq...
Maryam Morovati Mokhtari, Azim Soltanabadi, M. Feyzi et al.· ChemistrySelect· 0 citations
Ionic liquids (ILs) are now an established and ubiquitous material class. In energy applications and electroresponsive lubrication, their interfacial self-assembly is crucial for their properties. This in turn is determined by chemical structure and a local hierarchy of Coulombic, van der Waals, and solvophobic interac...
O. Hammond, Guillaume Bousrez, Stuart J. Brown et al.· Science Advances· 0 citations
We report a comprehensive bonding analysis of the nonpolar bonds H-H, Li-Li, and F-F and the polar bonds Li-H, H-F, and Li-F as well as the isoelectronic dications HeNe2+, BeHe2+ and BeNe2+. We also analyze the chemical bonds in the heavier halogen systems EF and ECl (E = Na-Cs). It is shown that the bonding interactio...
Ya-Hui Li, Cheng-Xiang Ding, Sudip Pan et al.· Journal of Chemical Theory a...· 0 citations
Hydridic hydrogen atoms, where hydrogen carries increased electron density, form a distinct class of noncovalent interactions, yet their structural and energetic characteristics remain poorly understood. Shallow multi-minima potential-energy surfaces and competing low-energy docking motifs make conventional NMR insuffi...
M. Lamanec, M. Marchi, S. H. Hossein Hejazi et al.· Chemical Science· 0 citations
ABSTRACT Crystalline hybrid networks containing metal coordination centers often disrupt continuous hydrogen‐bonding pathways, limiting their intrinsic proton conductivity. Here we report a suite of hydrogen‐bonded organic‐inorganic frameworks (HOIFs) composed of ionic/neutral organic and metal‐free inorganic building...
Jin Chen, Yong-Qiang Cheng, S. Teat et al.· Advancement of science· 0 citations
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