scholarly journals Efficient and selective hydrogen peroxide-mediated oxidation of sulfides in batch and segmented and continuous flow using a peroxometalate-based polymer immobilised ionic liquid phase catalyst

2015 ◽  
Vol 17 (3) ◽  
pp. 1559-1571 ◽  
Author(s):  
S. Doherty ◽  
J. G. Knight ◽  
M. A. Carroll ◽  
J. R. Ellison ◽  
S. J. Hobson ◽  
...  

Highly efficient sulfide oxidation has been achieved under segmented and continuous flow using a peroxometalate-based polymer immobilised ionic liquid phase catalyst.

2012 ◽  
Vol 14 (4) ◽  
pp. 925 ◽  
Author(s):  
Simon Doherty ◽  
Julian G. Knight ◽  
Jack R. Ellison ◽  
David Weekes ◽  
Ross W. Harrington ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (77) ◽  
pp. 73118-73131 ◽  
Author(s):  
S. Doherty ◽  
J. G. Knight ◽  
M. A. Carroll ◽  
A. R. Clemmet ◽  
J. R. Ellison ◽  
...  

Good conversion and high selectivity for sulfoxidation have been achieved under segmented and continuous flow using a polystyrene-based polymer immobilised ionic liquid phase (PIILP) peroxotungstate.


RSC Advances ◽  
2014 ◽  
Vol 4 (61) ◽  
pp. 32054-32062 ◽  
Author(s):  
Baochun Ma ◽  
Wei Zhao ◽  
Fuming Zhang ◽  
Yingshuai Zhang ◽  
Songyun Wu ◽  
...  

A new environmentally benign and highly efficient reaction-controlled phase-transfer catalyst for olefin epoxidation, sulfide and alcohol oxidation was developed.


2012 ◽  
Vol 9 (2) ◽  
pp. 863-868 ◽  
Author(s):  
Masoud Mokhtary ◽  
Mohammad Qandalee ◽  
Masoumeh Rastegar Niaki

A highly efficient method for the oxidation of sulfides to sulfoxides using oxalic acid dihydrate in the presence of hydrogen peroxide has been developed. A versatile procedure for the oxidation of sulfides to sulfoxides without any over-oxidation to sulfones has been reported. This procedure cleanly oxidizes sulfides to the corresponding sulfoxides in excellent yields at ambient temperature.


2011 ◽  
Vol 12 (8) ◽  
pp. 726-730 ◽  
Author(s):  
Gustavo P. Romanelli ◽  
Paula I. Villabrille ◽  
Cármen V. Cáceres ◽  
Patricia G. Vázquez ◽  
Pietro Tundo

2010 ◽  
Vol 39 (36) ◽  
pp. 8501 ◽  
Author(s):  
Ulrich Hintermair ◽  
Zenxing Gong ◽  
Ana Serbanovic ◽  
Mark J. Muldoon ◽  
Catherine C. Santini ◽  
...  

RSC Advances ◽  
2015 ◽  
Vol 5 (59) ◽  
pp. 47732-47739 ◽  
Author(s):  
Prasanta Kumar Bera ◽  
Naveen Gupta ◽  
Sayed H. R. Abdi ◽  
Noor-ul H. Khan ◽  
Rukhsana I. Kureshy ◽  
...  

This study represents a highly efficient sulfide oxidation catalytic system using a non-toxic Ti-catalyst and environmentally benign aqueous hydrogen peroxide.


1998 ◽  
Vol 76 (6) ◽  
pp. 770-775 ◽  
Author(s):  
Antonio Marques ◽  
Massimo di Matteo ◽  
Marie-Françoise Ruasse

The efficiency of various metallo-phtalocyanines (Pht) and -tetraphenylporphyrins (TPP) as catalysts for the H2O2 oxidations of dibenzylsulfide, phenylchloroethylsulfide, and thioanisole is investigated in ethanol and acetonitrile, using imidazole as a cocatalyst. Neither PhtNiII nor TPPCoII exhibits any catalytic activity. PhtMnII and TPPMnIIICl accelerate markedly these reactions but do not promote quantitative oxidations, at most 70% of the sulfides being transformed into sulfoxides. In contrast, with PhtFeII sulfoxides are obtained with a 100% yield from sulfides. Finally, the only catalyst able to oxidize sulfides rapidly (<5 min), completely and quantitatively (100% sulfone) is TPPFeIIICl in EtOH. The absence of any by-product, disulfide in particular, suggests that a free sulfenium radical cation is not an active intermediate in these reactions. The marked differences in the behaviour of TPPMnIIICl and TPPFeIII Cl are analyzed by comparing the rates of the catalyst decomposition, of the sulfoxide and sulfone formation as a function of the hydrogen peroxide concentration. The results are discussed in terms of a competition between the several oxidative pathways and a possible mechanism for the oxygen transfer to sulfides.Key words: sulfide, oxidation, H2O2, manganese(III) or iron(III) tetraphenylporphyrin.


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