The Unique Gas-Phase Chemistry of the [AuO]+ /CH4 Couple: Selective Oxygen-Atom Transfer to, Rather than Hydrogen-Atom Abstraction from, Methane

2016 ◽  
Vol 55 (36) ◽  
pp. 10877-10880 ◽  
Author(s):  
Shaodong Zhou ◽  
Jilai Li ◽  
Maria Schlangen ◽  
Helmut Schwarz
2014 ◽  
Vol 16 (48) ◽  
pp. 26617-26623 ◽  
Author(s):  
Xiao-Nan Wu ◽  
Hai-Tao Zhao ◽  
Jilai Li ◽  
Maria Schlangen ◽  
Helmut Schwarz

The metal center of [Zn(OH)]+ serves as active site in the regiospecific hydride transfer to generate [i-C3H7]+ as major product in the reaction with C3H8. In the [Zn(OH)]+–C3H8 system, a high regioselectivity features the remarkable chemoselectivity.


2010 ◽  
Vol 132 (12) ◽  
pp. 4336-4343 ◽  
Author(s):  
Maria Elisa Crestoni ◽  
Simonetta Fornarini ◽  
Francesco Lanucara ◽  
Jeffrey J. Warren ◽  
James M. Mayer

2015 ◽  
Vol 54 (15) ◽  
pp. 7152-7164 ◽  
Author(s):  
Mainak Mitra ◽  
Hassan Nimir ◽  
Serhiy Demeshko ◽  
Satish S. Bhat ◽  
Sergey O. Malinkin ◽  
...  

1998 ◽  
Vol 120 (31) ◽  
pp. 7869-7874 ◽  
Author(s):  
Maria Anita Mendes ◽  
Luiz Alberto B. Moraes ◽  
Regina Sparrapan ◽  
Marcos N. Eberlin ◽  
Risto Kostiainen ◽  
...  

2022 ◽  
Author(s):  
Sandip Munshi ◽  
Arup Sinha ◽  
Solomon Yiga ◽  
Sridhar Banerjee ◽  
Reena Singh ◽  
...  

The reactivities of Fe(iv) oxido complexes of two pentadentate ligands are related to steric and electronic properties of the ligands.


Cyclo hexyl methyl sulphide is oxidized quantitatively to the sulphoxide by alcoholic solutions of cyclo hexenyl and t -butyl hydroperoxides at moderate temperatures. Kinetically the oxida­tion appears to be a simple bimolecular reaction, first-order with respect to both the sulphide and hydroperoxide. However, the reaction rates vary in different alcohols in the order of varying solvent acidity, and correspondingly the addition of much stronger acids produces powerful catalysis. The solvent and the acids clearly play a part in the reaction, and it is concluded that the actual oxidant is a cyclic complex between the hydroperoxide and a hydrogen-donating molecule, oxygen atom transfer to the sulphide being promoted by a synchronous hydrogen atom exchange process within the complex. Energies and entropies of activation for the oxidation under various conditions are reported and their significance discussed.


2007 ◽  
Vol 129 (44) ◽  
pp. 13646-13652 ◽  
Author(s):  
William W. Y. Lam ◽  
Wai-Lun Man ◽  
Chi-Fai Leung ◽  
Chun-Yuen Wong ◽  
Tai-Chu Lau

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