Reaction of carbon oxides with an ethylene-bridged PH/B Lewis pair

2021 ◽  
Vol 50 (10) ◽  
pp. 3523-3528
Author(s):  
Qiu Sun ◽  
Constantin G. Daniliuc ◽  
Gerald Kehr ◽  
Gerhard Erker

The ethylene-bridged frustrated Lewis pair, formed by hydroboration of the Mes*P(H)-vinyl phosphane with Piers' borane [HB(C6F5)2], reacted with the CO/ HB(C6F5)2 pair and also with carbon dioxide.

1934 ◽  
Vol 10 (6) ◽  
pp. 743-758 ◽  
Author(s):  
E. H. Boomer ◽  
H. E. Morris

Numerous experiments have been carried out on the decomposition of alcohol, alcohol and water, and alcohol and carbon dioxide mixtures over poly-component catalysts at temperatures up to 500 °C. Quantitative data on the gaseous and the liquid products were obtained. The properties of the poly-component catalysts, as evidenced by the simple primary and secondary reactions, have been shown to be qualitatively those of the single components.Methane can be produced in one or more of several secondary reactions, namely, the decomposition of acetaldehyde, the hydrogenation of carbon oxides and the decomposition of ethylene. Ethane can be produced in one or both of two reactions consisting of auto-oxidation and reduction of the alcohol, or the secondary hydrogenation of ethylene, confirming previous work. Carbon dioxide, in most cases, is formed as a result of the water-gas reaction and the decomposition of carbon monoxide. In other cases its origin is obscure. The results of certain experiments in which carbon dioxide and hydrogen were the major constituents of the off-gas cannot be explained in the same way. Reactions involving ketene decomposition and polymerization, and hydration of alcohol, have been suggested as possible explanations.


2011 ◽  
Vol 47 (6) ◽  
pp. 1833 ◽  
Author(s):  
Xiaoxi Zhao ◽  
Douglas W. Stephan

Author(s):  
R. R. Baker

AbstractFlue-cured Virginia tobacco has been heated in nitrogen and nitrogen/oxygen mixtures under flow conditions, and the rate of formation of carbon monoxide and carbon dioxide has been determined as a function of temperature, heating rate, and proportion of oxygen in the gas. When the tobacco is heated in nitrogen at heating rates comparable to those in a smouldering cigarette, 27 % of the carbon content of the tobacco is converted to carbon oxides. Both carbon oxides show two distinct formation regions: a low-temperature region (about 100°-450°C), and a high-temperature region (about 550°-900°C). These temperature limits are almost identical to those predicted from studies on the combustion coal of a cigarette burning in air. When tobacco, or the carbonaceous residue remaining after the pyrolysis experiments, is heated in nitrogen / oxygen mixtures, the total amount of carbon converted to carbon monoxide and carbon dioxide is independent of heating rate, but the relative proportions of the two oxides are strongly dependent on heating rate. At the lower heating rate, proportionally less carbon monoxide, and more carbon dioxide, is produced. Under oxidation conditions, about 70 % of both carbon oxides formed in the low-temperature region (100°-450°C) are produced by tobacco decomposition reactions, whereas in the high-temperature region about 10-20 % of the carbon monoxide, and 2-9 % of the carbon dioxide, are produced by tobacco decomposition.


2017 ◽  
Vol 8 (3) ◽  
pp. 2457-2463 ◽  
Author(s):  
Tongdao Wang ◽  
Long Wang ◽  
Constantin G. Daniliuc ◽  
Kamil Samigullin ◽  
Matthias Wagner ◽  
...  

The reversible enamine/HB(C6F5)2 Lewis adduct reacts with CO by selective head to tail coupling whereas it reacts with NO via a vicinal N/B Lewis pair to give a head to head NO/NO coupling product.


2019 ◽  
Author(s):  
Daniel W. Beh ◽  
Warren Piers ◽  
Benjamin S. Gelfand ◽  
Jian-Bin Lin

A scandium hydridoborate complex supported by the dianionic pentadentate ligand B<sub>2</sub>Pz<sub>4</sub>Py is prepared via hydride abstraction from the previously reported scandium hydride complex with <i>tris</i>-pentafluorophenyl borane. Exposure of [(B<sub>2</sub>Pz<sub>4</sub>Py)Sc][HB(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>] to CO<sub>2</sub> immediately forms [(B<sub>2</sub>Pz<sub>4</sub>Py)Sc][HCOOB(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>] at room temperature. The formatoborate complex can also be synthesized directly from the starting material (B<sub>2</sub>Pz<sub>4</sub>Py)ScCl with Et<sub>3</sub>SiH and B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub> while in the presence of an atmosphere of CO<sub>2</sub> in 81% yield. This compound was evaluated as the transition metal component of a tandem deoxgenative CO<sub>2</sub> hydrosilation catalyst. At 5% loadings, complete consumption of Et<sub>3</sub>SiH was observed along with CO<sub>2</sub> reduction products, but conversion to an inactive scandium complex identified as (B<sub>2</sub>Pz<sub>4</sub>Py)ScOSiEt<sub>3</sub> was observed


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