Effect of Acidity of Ionic Liquids on Hydrogen Bonding Interaction between Ionic Liquids and Lignin Monomers

2018 ◽  
Vol 3 (12) ◽  
pp. 3570-3574 ◽  
Author(s):  
Sandip K. Singh ◽  
Ajeet Singh
Keyword(s):  
Hydrogen Bonding ◽  
Ionic Liquids ◽  
Hydrogen Bonding Interaction ◽  
Bonding Interaction

scholarly journals Porous liquid zeolites: hydrogen bonding-stabilized H-ZSM-5 in branched ionic liquids

Nanoscale ◽  
2019 ◽  
Vol 11 (4) ◽  
pp. 1515-1519 ◽  
Author(s):  
Peipei Li ◽  
Hao Chen ◽  
Jennifer A. Schott ◽  
Bo Li ◽  
Yaping Zheng ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Ionic Liquids ◽  
Hydrogen Bonding Interaction ◽  
Bonding Interaction

The porous liquid zeolites with permanent porosity could be fabricated by exploiting the hydrogen bonding interaction between the alkane chains of branched ionic liquids and the Brønsted sites in H-form zeolites.

Highly efficient CO2 capture by carbonyl-containing ionic liquids through Lewis acid–base and cooperative C–H⋯O hydrogen bonding interaction strengthened by the anion

2014 ◽  
Vol 50 (95) ◽  
pp. 15041-15044 ◽  
Author(s):  
Fang Ding ◽  
Xi He ◽  
Xiaoyan Luo ◽  
Wenjun Lin ◽  
Kaihong Chen ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Ionic Liquids ◽  
Lewis Acid ◽  
Co2 Capture ◽  
Significant Enhancement ◽  
Hydrogen Bonding Interaction ◽  
Acid Base ◽  
Highly Efficient ◽  
Bonding Interaction

Carbonyl-containing anion-functionalized ionic liquids exhibit a significant enhancement in CO2 capacity and excellent reversibility.

Understanding the mechanism of LCST phase separation of mixed ionic liquids in water by MD simulations

2016 ◽  
Vol 18 (33) ◽  
pp. 23238-23245 ◽  
Author(s):  
Yuling Zhao ◽  
Huiyong Wang ◽  
Yuanchao Pei ◽  
Zhiping Liu ◽  
Jianji Wang
Keyword(s):  
Ionic Liquid ◽  
Hydrogen Bonding ◽  
Ionic Liquids ◽  
Phase Separation ◽  
Amino Acid ◽  
Driving Force ◽  
Md Simulations ◽  
Liquid Mixtures ◽  
Hydrogen Bonding Interaction ◽  
Bonding Interaction

Hydrogen bonding interaction between amino acid anions is the driving force for the phase separation of aqueous ionic liquid mixtures.

Highly efficient separation of 5-hydroxymethylfurfural from imidazolium-based ionic liquids

2021 ◽  
Author(s):  
Huiyong Wang ◽  
Jingjing Cui ◽  
Yuling Zhao ◽  
Zhiyong Li ◽  
Jianji Wang
Keyword(s):  
Hydrogen Bond ◽  
Hydrogen Bonding ◽  
Ionic Liquids ◽  
Hydrogen Bonding Interaction ◽  
Hydrogen Bond Acceptor ◽  
Efficient Separation ◽  
Highly Efficient ◽  
Bonding Interaction

The hydrogen bond acceptor ability of solvents, the interactions between the anion and cation of ILs, and the hydrogen bonding interaction of the anion with 5-HMF play important roles in the separation of 5-HMF from ILs.

Radical Enzymes Control the Chemistry of Their Highly Reactive Intermediates Using the Quantum Coulombic Effect

2020 ◽  
Author(s):  
Hossein Khalilian ◽  
Gino A. DiLabio
Keyword(s):  
Hydrogen Bonding ◽  
Molecular Orbital ◽  
Reactive Intermediates ◽  
Hydrogen Bonding Interaction ◽  
Orbital Ordering ◽  
Dynamic Nature ◽  
Radical Intermediate ◽  
Highest Occupied Molecular Orbital ◽  
Bonding Interaction ◽  
Close Proximity

Here, we report an exquisite strategy that the B12 enzymes exploit to manipulate the reactivity of their radical intermediate (Adenosyl radical). Based on the quantum-mechanic calculations, these enzymes utilize a little known long-ranged through space quantum Coulombic effect (QCE). The QCE causes the radical to acquire an electronic structure that contradicts the Aufbau Principle: The singly-occupied molecular orbital (SOMO) is no longer the highest-occupied molecular orbital (HOMO) and the radical is unable to react with neighbouring substrates. The dynamic nature of the enzyme and its structure is expected to be such that the reactivity of the radical is not restored until it is moved into close proximity of the target substrate. We found that the hydrogen bonding interaction between the nearby conserved glutamate residue and the ribose ring of Adenosyl radical plays a crucial role in manipulating the orbital ordering

Radical Enzymes Control the Chemistry of Their Highly Reactive Intermediates Using the Quantum Coulombic Effect

2020 ◽  
Author(s):  
Hossein Khalilian ◽  
Gino A. DiLabio
Keyword(s):  
Hydrogen Bonding ◽  
Molecular Orbital ◽  
Reactive Intermediates ◽  
Hydrogen Bonding Interaction ◽  
Orbital Ordering ◽  
Dynamic Nature ◽  
Radical Intermediate ◽  
Highest Occupied Molecular Orbital ◽  
Bonding Interaction ◽  
Close Proximity

Here, we report an exquisite strategy that the B12 enzymes exploit to manipulate the reactivity of their radical intermediate (Adenosyl radical). Based on the quantum-mechanic calculations, these enzymes utilize a little known long-ranged through space quantum Coulombic effect (QCE). The QCE causes the radical to acquire an electronic structure that contradicts the Aufbau Principle: The singly-occupied molecular orbital (SOMO) is no longer the highest-occupied molecular orbital (HOMO) and the radical is unable to react with neighbouring substrates. The dynamic nature of the enzyme and its structure is expected to be such that the reactivity of the radical is not restored until it is moved into close proximity of the target substrate. We found that the hydrogen bonding interaction between the nearby conserved glutamate residue and the ribose ring of Adenosyl radical plays a crucial role in manipulating the orbital ordering

Sign in / Sign up

Export Citation Format

Share Document