scholarly journals Synthesis of Cyclic Carbonates from Olefin Oxides and Carbon Dioxide. Part 1. Catalysis by Ionic Liquids

2016 ◽  
Vol 16 (3) ◽  
pp. 6-16
Author(s):  
A. V. Sulimov ◽  
A. V. Ovcharova ◽  
A. A. Ovcharov ◽  
T. A. Ryabova ◽  
G. M. Kravchenko ◽  
...  
2016 ◽  
Vol 8 (4) ◽  
pp. 300-309 ◽  
Author(s):  
A. V. Sulimov ◽  
A. V. Ovcharova ◽  
A. A. Ovcharov ◽  
T. A. Ryabova ◽  
G. M. Kravchenko ◽  
...  

2013 ◽  
Vol 30 (11) ◽  
pp. 1973-1984 ◽  
Author(s):  
Dong-Woo Kim ◽  
Roshith Roshan ◽  
Jose Tharun ◽  
Amal Cherian ◽  
Dae-Won Park

2019 ◽  
Vol 19 (1) ◽  
pp. 5-18
Author(s):  
A. V. Sulimov ◽  
A. V. Ovcharova ◽  
Yu. K. Sulimova

The review paper deals with catalytic systems based on porphyrin complexes of metals used for stimulation of reactions of olefins and carbon dioxide. It is shown that these porlhyrin complexes may behave as effective catalysts for carboxylation of epoxides. Specific features of catalysis of the interaction between oxiranes and carbon dioxide in the presence of homogeneous and heterogenized porphyrin complexes of metals, including those comprising various promoters, are considered.


2018 ◽  
Vol 71 (6) ◽  
pp. 407
Author(s):  
Shuang Yue ◽  
Qian Song ◽  
Shuliang Zang ◽  
Guichun Deng ◽  
Jun Li

Various amino-functional ionic liquids were developed as homogeneous catalysts for the cycloaddition of carbon dioxide to different epoxides yielding the corresponding cyclic carbonates under metal- and solvent-free conditions. The effects of reaction temperature, reaction time, CO2 pressure, and the amount of catalyst on the cycloaddition reaction were investigated. The catalysts could be easily recovered after the reaction and then reused at least eight times without noticeable loss of activity and selectivity. Reaction kinetic studies were undertaken, the reaction was apparently first order with respect to the concentration of epoxide and catalyst. Furthermore, the rate constants were determined over a temperature range of 100–130°C and the activation energy was determined to be 45.9 kJ mol−1. Finally, a possible reaction mechanism was proposed. The amino-functional ionic liquids showed the advantage of high catalytic activity and were easily recyclable for CO2 chemical fixation into valuable chemicals.


2014 ◽  
Vol 4 (6) ◽  
pp. 1513-1528 ◽  
Author(s):  
Qing He ◽  
Jeremy W. O'Brien ◽  
Kayla A. Kitselman ◽  
Lindsay E. Tompkins ◽  
Gregory C. T. Curtis ◽  
...  

In this mini-review, progress made in the use of ionic liquid catalysts and related systems for cycloaddition reactions of carbon dioxide with epoxides is described with the primary focus on results from the past eight years.


2010 ◽  
Vol 352 (13) ◽  
pp. 2233-2240 ◽  
Author(s):  
Zhen-Zhen Yang ◽  
Liang-Nian He ◽  
Cheng-Xia Miao ◽  
Sébastien Chanfreau

2016 ◽  
Vol 91 (11) ◽  
pp. 2827-2833 ◽  
Author(s):  
Katarzyna Jasiak ◽  
Agnieszka Siewniak ◽  
Katarzyna Kopczyńska ◽  
Anna Chrobok ◽  
Stefan Baj

2018 ◽  
Vol 71 (3) ◽  
pp. 181 ◽  
Author(s):  
Peter Goodrich ◽  
H. Q. Nimal Gunaratne ◽  
Lili Jin ◽  
Yuntao Lei ◽  
Kenneth R. Seddon

An efficient and greener synthesis of unsymmetrical organic carbonates mediated by Hünig’s base-appended basic ionic liquids, via carbon dioxide conversion, is described here. These ionic liquids were found to be effective bases for the fixation of carbon dioxide by various alcohols and benzyl bromide, at room temperature. When the alcohol and the halide functionalities are present within the same substrate, the reaction cleanly produces a cyclic carbonate. These functionalised basic ionic liquids were fully recyclable with no loss product yields.


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