scholarly journals Inside the reaction mechanism of direct CO2 conversion to DME over zeolite-based hybrid catalysts

2021 ◽  
Vol 294 ◽  
pp. 120255
Author(s):  
G. Bonura ◽  
S. Todaro ◽  
L. Frusteri ◽  
I. Majchrzak-Kucęba ◽  
D. Wawrzyńczak ◽  
...  
2020 ◽  
Vol 49 (25) ◽  
pp. 8478-8497 ◽  
Author(s):  
Michael D. Higham ◽  
Matthew G. Quesne ◽  
C. Richard A. Catlow

Density functional methods are applied to explore the reaction mechanism for CO2 hydrogenation to methanol over low-index Cu surfaces, namely Cu(110) and Cu(100).


2015 ◽  
Vol 17 (16) ◽  
pp. 11088-11094 ◽  
Author(s):  
Ellie L. Uzunova ◽  
Nicola Seriani ◽  
Hans Mikosch

The CO2 hydrogenation to methanol using dissociated water as the hydrogen source proceeds via stable carboxyl, formic acid and formaldehyde intermediates.


2020 ◽  
Vol 60 (4) ◽  
pp. 508-515
Author(s):  
L. Frusteri ◽  
G. Bonura ◽  
C. Cannilla ◽  
S. Todaro ◽  
G. Giordano ◽  
...  

Catalysts ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 325 ◽  
Author(s):  
Carla Calabrese ◽  
Francesco Giacalone ◽  
Carmela Aprile

The conversion of carbon dioxide into valuable chemicals such as cyclic carbonates is an appealing topic for the scientific community due to the possibility of valorizing waste into an inexpensive, available, nontoxic, and renewable carbon feedstock. In this regard, last-generation heterogeneous catalysts are of great interest owing to their high catalytic activity, robustness, and easy recovery and recycling. In the present review, recent advances on CO2 cycloaddition to epoxide mediated by hybrid catalysts through organometallic or organo-catalytic species supported onto silica-, nanocarbon-, and metal–organic framework (MOF)-based heterogeneous materials, are highlighted and discussed.


2021 ◽  
Vol 61 (9) ◽  
pp. 1081-1081
Author(s):  
L. Frusteri ◽  
G. Bonura ◽  
C. Cannilla ◽  
S. Todaro ◽  
G. Giordano ◽  
...  

Author(s):  
Tomasz J. Idzik ◽  
Zofia M. Myk ◽  
Łukasz Struk ◽  
Magdalena Perużyńska ◽  
Gabriela Maciejewska ◽  
...  

Triisopropylsilyltrifluoromethanesulfonate can be effectively used for the arylation of a wide range of enelactams. The multinuclear NMR study provided deep insights into the reaction mechanism.


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