scholarly journals Cobalt‐Iron‐Manganese Catalysts for the Conversion of End‐of‐Life‐Tire‐Derived Syngas into Light Terminal Olefins

2018 ◽  
Vol 24 (18) ◽  
pp. 4597-4606 ◽  
Author(s):  
Jan P. Falkenhagen ◽  
Lise Maisonneuve ◽  
Pasi P. Paalanen ◽  
Nathalie Coste ◽  
Nicolas Malicki ◽  
...  
2020 ◽  
Vol 24 (14) ◽  
pp. 1582-1609
Author(s):  
Mohammad Dodangeh ◽  
Ali Ramazani ◽  
Malek-Taher Maghsoodlou ◽  
Armin Zarei ◽  
Sobhan Rezayati

Catalytic C-H activation is a powerful method for organic synthesis. In recent years, scientists have made great progress by developing transitional metals for catalyzing CH functionalization reaction. In this review, we summarized and highlighted recent progress in C-H activation with copper, cobalt, iron, manganese, and nickel as catalysts.


ChemSusChem ◽  
2021 ◽  
Author(s):  
Troels Skrydstrup ◽  
Laurynas Gausas ◽  
Bjarke Donslund ◽  
Steffan Kristensen

2003 ◽  
Vol 07 (07) ◽  
pp. 508-520 ◽  
Author(s):  
Joe Obirai ◽  
Nazaré Pereira Rodrigues ◽  
Fethi Bedioui ◽  
Tebello Nyokong

A new family of pyrrole substituted metallophthalocyanine complexes, namely cobalt(II), iron(II), manganese(III), nickel(II) and zinc(II) tetrakis-4-(pyrrol-1-yl)phenoxy phthalocyanines (noted as M ( TPhPyrPc ), where M is the metallic cation) have been synthesized and fully characterized. In particular, the UV-visible spectra of the iron and nickel complexes showed extensive aggregation even at low concentrations. The cyclic voltammetry of the cobalt, iron and manganese complexes showed three to four redox couples assigned to metal and ring based processes. Spectroelectrochemistry of the manganese derivative confirmed that the synthesized complex is Mn III( TPhPyrPc -2) and that the reduction of Mn II( TPhPyrPc -2) to be centred on the ring and rather than on the metal, forming the Mn II( TPhPyrPc -4) species. Also, the electrochemical polymerization of these newly synthesized pyrrole-substituted phthalocyanines has been demonstrated in the case of the cobalt complex and the electrocatalytic activity of the obtained film has been tested towards the oxidation of L-cysteine.


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