Simultaneous recovery of copper and manganese from exotic copper ore in acid chloride media using cane molasses as the reducing agent

2021 ◽  
Vol 199 ◽  
pp. 105531
Author(s):  
L. Velásquez-Yévenes ◽  
Ricardo Lasnibat
Author(s):  
DENNIS H. BURNS ◽  
MICHAEL W. BURDEN ◽  
YUE HU LI

A method for the preparation of an α-formylated pyrrole or dipyrromethane which contains an electron-withdrawing β-acetyl is described. Formylation proceeds directly from the corresponding acid pyrrole or dipyrromethane without the need of the usual two-step acid decarboxylation/formylation procedure. The acid is first transformed into its acid chloride with oxalyl chloride, followed by reduction to the aldehyde with the mild reducing agent sodium triacetoxyborohydride, in a one-pot reaction. The non-basic acylating reagent PR 3 is necessary both for acyl chloride formation and for the reduction to succeed.


INEOS OPEN ◽  
2020 ◽  
Vol 3 ◽  
Author(s):  
O. I. Afanasyev ◽  
◽  
D. Chusov ◽  

Carbon monoxide is a unique reducing agent that is only gaining popularity in organic chemistry. This review highlights the main approaches to the application of CO as a reducing agent, summarizes and critically analyzes the key trends in this field, and describes the current development prospects. Potentially the most selective and efficient route for the realization of these processes is demonstrated.


1967 ◽  
Vol 56 (1_Suppl) ◽  
pp. S62
Author(s):  
M. Wenzel ◽  
K. Pollow
Keyword(s):  

2018 ◽  
Author(s):  
Chandan Dey ◽  
Ronny Neumann

<p>A manganese substituted Anderson type polyoxometalate, [MnMo<sub>6</sub>O<sub>24</sub>]<sup>9-</sup>, tethered with an anthracene photosensitizer was prepared and used as catalyst for CO<sub>2</sub> reduction. The polyoxometalate-photosensitizer hybrid complex, obtained by covalent attachment of the sensitizer to only one face of the planar polyoxometalate, was characterized by NMR, IR and mass spectroscopy. Cyclic voltammetry measurements show a catalytic response for the reduction of carbon dioxide, thereby suggesting catalysis at the manganese site on the open face of the polyoxometalate. Controlled potentiometric electrolysis showed the reduction of CO<sub>2</sub> to CO with a TOF of ~15 sec<sup>-1</sup>. Further photochemical reactions showed that the polyoxometalate-anthracene hybrid complex was active for the reduction of CO<sub>2</sub> to yield formic acid and/or CO in varying amounts dependent on the reducing agent used. Control experiments showed that the attachment of the photosensitizer to [MnMo<sub>6</sub>O<sub>24</sub>]<sup>9-</sup> is necessary for photocatalysis.</p><div><br></div>


Author(s):  
Walber Ronconi dos Santos ◽  
Edson Soares ◽  
Renato Siqueira

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