scholarly journals Paradigm for efficient synthesis of bio-based polycarbonate with deep eutectic solvents as catalysts by inhibiting the degradation of molecular chains

2021 ◽  
Author(s):  
Weiwei Wang ◽  
Zifeng Yang ◽  
Yaqin Zhang ◽  
Hongyan He ◽  
Wenjuan Fang ◽  
...  

In this study, an efficient catalytic system composed of deep eutectic solvents (DESs) was developed by adjusting the basicity of hydrogen bond donors (HBDs) to synthesize poly (isosorbide) carbonate (PIC)...

2019 ◽  
Vol 48 (27) ◽  
pp. 10199-10209 ◽  
Author(s):  
Ming-Yu Zhao ◽  
Jian-Nan Zhu ◽  
Peng Li ◽  
Wei Li ◽  
Ting Cai ◽  
...  

Seven transition metal–organic frameworks with structures ranging from one-dimensional chains to three-dimensional networks have been synthesized in deep eutectic solvents.


2020 ◽  
Vol 8 (35) ◽  
pp. 13408-13417 ◽  
Author(s):  
Wen-Jing Jiang ◽  
Jian-Bo Zhang ◽  
Ya-Ting Zou ◽  
Hai-Long Peng ◽  
Kuan Huang

RSC Advances ◽  
2021 ◽  
Vol 11 (48) ◽  
pp. 30102-30108
Author(s):  
Setareh Rostami-Javanroudi ◽  
Masoud Moradi ◽  
Kiomars Sharafi ◽  
Nazir Fattahi

In this research, several novel hydrophobic deep eutectic solvents (DESs) were prepared using methyltrioctylammonium chloride (MTOAC) as the hydrogen bond acceptor (HBA) and different types of straight chain alcohols as hydrogen bond donors (HBDs).


2019 ◽  
Vol 55 (69) ◽  
pp. 10253-10256 ◽  
Author(s):  
Dinis O. Abranches ◽  
Mónia A. R. Martins ◽  
Liliana P. Silva ◽  
Nicolas Schaeffer ◽  
Simão P. Pinho ◽  
...  

An abnormal strong interaction was identified, which was found to be the key to prepare non-ionic DES, that may be classified as type V.


2019 ◽  
Vol 21 (11) ◽  
pp. 3116-3126 ◽  
Author(s):  
Katarzyna Haraźna ◽  
Karolina Walas ◽  
Patrycja Urbańska ◽  
Tomasz Witko ◽  
Wojciech Snoch ◽  
...  

Polyhydroxyalkanoate monomers can serve as deep eutectic solvents components.


2017 ◽  
Vol 53 (72) ◽  
pp. 9983-9985 ◽  
Author(s):  
J. C. Goeltz ◽  
L. N. Matsushima

Metal-free deep eutectic solvents composed of hydrogen bond donors and viologen-based ammonium salts exhibit reversible electrochemistry with viologen concentrations of 4.2 M and freezing points near room temperature.


Catalysts ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 655
Author(s):  
Chiara Allegretti ◽  
Francesco G. Gatti ◽  
Stefano Marzorati ◽  
Letizia Anna Maria Rossato ◽  
Stefano Serra ◽  
...  

The use of Reactive Deep Eutectic Solvents (RDESs) in the preparation of polar head modified phospholipids (PLs) with phospholipase D (PLD)-catalyzed biotransformations has been investigated. Natural phosphatidylcholine (PC) has been submitted to PLD-catalyzed transphosphatidylations using a new reaction medium composed by a mixture of RDES/buffer. Instead of exploiting deep eutectic solvents conventionally, just as the reaction media, these solvents have been designed here in order to contribute actively to the synthetic processes by participating as reagents. RDESs were prepared using choline chloride or trimethyl glycine as hydrogen-bond acceptors and glycerol or ethylene glycol, as hydrogen-bond donors as well as nucleophiles for choline substitution. Specifically designed RDES/buffer reaction media allowed the obtainment of PLs with optimized yields in the perspective of a sustainable process implementation.


Molecules ◽  
2021 ◽  
Vol 26 (23) ◽  
pp. 7167
Author(s):  
Ze Wang ◽  
Zonghua Wang ◽  
Jie Chen ◽  
Congyi Wu ◽  
Dezhong Yang

Recently, deep eutectic solvents (DESs), a new type of solvent, have been studied widely for CO2 capture. In this work, the anion-functionalized deep eutectic solvents composed of phenol-based ionic liquids (ILs) and hydrogen bond donors (HBDs) ethylene glycol (EG) or 4-methylimidazole (4CH3-Im) were synthesized for CO2 capture. The phenol-based ILs used in this study were prepared from bio-derived phenols carvacrol (Car) and thymol (Thy). The CO2 absorption capacities of the DESs were determined. The absorption mechanisms by the DESs were also studied using nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR), and mass spectroscopy. Interestingly, the results indicated that CO2 reacted with both the phenolic anions and EG, generating the phenol-based carbonates and the EG-based carbonates, when CO2 interacted with the DESs formed by the ILs and EG. However, CO2 only reacted with the phenolic anions when the DESs formed by the ILs and 4CH3-Im. The results indicated that the HBDs impacted greatly on the CO2 absorption mechanism, suggesting the mechanism can be tuned by changing the HBDs, and the different reaction pathways may be due to the steric hinderance differences of the functional groups of the HBDs.


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