The Initial Stages of Solid Acid-Catalyzed Reactions of Adsorbed Propane. A Mechanistic Study by in Situ MAS NMR

2004 ◽  
Vol 126 (2) ◽  
pp. 599-606 ◽  
Author(s):  
Mohamed Haouas ◽  
Stéphane Walspurger ◽  
Francis Taulelle ◽  
Jean Sommer
2013 ◽  
Vol 53 (2) ◽  
pp. 479-482 ◽  
Author(s):  
Aleksei Vjunov ◽  
Mary Y. Hu ◽  
Ju Feng ◽  
Donald M. Camaioni ◽  
Donghai Mei ◽  
...  

2013 ◽  
Vol 126 (2) ◽  
pp. 489-492 ◽  
Author(s):  
Aleksei Vjunov ◽  
Mary Y. Hu ◽  
Ju Feng ◽  
Donald M. Camaioni ◽  
Donghai Mei ◽  
...  

ChemCatChem ◽  
2013 ◽  
Vol 5 (6) ◽  
pp. 1531-1537 ◽  
Author(s):  
Trupti V. Kotbagi ◽  
Ankush V. Biradar ◽  
Shubhangi B. Umbarkar ◽  
Mohan K. Dongare

2020 ◽  
Vol 481 ◽  
pp. 110192 ◽  
Author(s):  
Nicolás M. Bertero ◽  
Andrés F. Trasarti ◽  
María C. Acevedo ◽  
Alberto J. Marchi ◽  
Carlos R. Apesteguía

ChemSusChem ◽  
2012 ◽  
Vol 5 (2) ◽  
pp. 430-437 ◽  
Author(s):  
Joseph Zakzeski ◽  
Ruud J. H. Grisel ◽  
Arjan T. Smit ◽  
Bert M. Weckhuysen

Catalysts ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 1143
Author(s):  
Maria Luisa Testa ◽  
Valeria La Parola

Acid catalysis is widely used in the chemical industry, and nowadays many efforts are being focused on replacing the more common homogeneous catalysts with heterogeneous ones in order to make greener the industrial processes. In this perspective, sulfonic solid acid materials represent a valid alternative to the homogenous mineral acid in several acid catalyzed reactions. In this minireview, an overview of the recent advances on the preparation, stability and application of these materials is reported. Special attention is addressed to the sustainability of the considered processes, starting from the catalyst’s preparation, the use of green solvents and reducing the possible reaction steps. Ways to tackle the main drawback represented by easy leaching of acid groups are described. For an easy catalyst recovery, the use of a magnetic core in a catalyst particle, with the related synthetic approaches, is also illustrated. Finally, a section is dedicated to the principal characterization techniques to identify the structural properties of the catalysts.


2018 ◽  
Author(s):  
Haley Albright ◽  
Paul S. Riehl ◽  
Christopher C. McAtee ◽  
Jolene P. Reid ◽  
Jacob R. Ludwig ◽  
...  

<div>Catalytic carbonyl-olefin metathesis reactions have recently been developed as a powerful tool for carbon-carbon bond</div><div>formation. However, currently available synthetic protocols rely exclusively on aryl ketone substrates while the corresponding aliphatic analogs remain elusive. We herein report the development of Lewis acid-catalyzed carbonyl-olefin ring-closing metathesis reactions for aliphatic ketones. Mechanistic investigations are consistent with a distinct mode of activation relying on the in situ formation of a homobimetallic singly-bridged iron(III)-dimer as the active catalytic species. These “superelectrophiles” function as more powerful Lewis acid catalysts that form upon association of individual iron(III)-monomers. While this mode of Lewis acid activation has previously been postulated to exist, it has not yet been applied in a catalytic setting. The insights presented are expected to enable further advancement in Lewis acid catalysis by building upon the activation principle of “superelectrophiles” and broaden the current scope of catalytic carbonyl-olefin metathesis reactions.</div>


2019 ◽  
Author(s):  
Przemyslaw Rzepka ◽  
Zoltán Bacsik ◽  
Andrew J. Pell ◽  
Niklas Hedin ◽  
Aleksander Jaworski

Formation of CO<sub>3</sub><sup>2-</sup> and HCO<sub>3</sub><sup>-</sup> species without participation of the framework oxygen atoms upon chemisorption of CO<sub>2</sub> in zeolite |Na<sub>12</sub>|-A is revealed. The transfer of O and H atoms is very likely to have proceeded via the involvement of residual H<sub>2</sub>O or acid groups. A combined study by solid-state <sup>13</sup>C MAS NMR, quantum chemical calculations, and <i>in situ</i> IR spectroscopy showed that the chemisorption mainly occurred by the formation of HCO<sub>3</sub><sup>-</sup>. However, at a low surface coverage of physisorbed and acidic CO<sub>2</sub>, a significant fraction of the HCO<sub>3</sub><sup>-</sup> was deprotonated and transformed into CO<sub>3</sub><sup>2-</sup>. We expect that similar chemisorption of CO<sub>2</sub> would occur for low-silica zeolites and other basic silicates of interest for the capture of CO<sub>2</sub> from gas mixtures.


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