Redox Properties of Tanaka’s Water Oxidation Catalyst: Redox Noninnocent Ligands Dominate the Electronic Structure and Reactivity

2011 ◽  
Vol 50 (13) ◽  
pp. 5946-5957 ◽  
Author(s):  
Soumya Ghosh ◽  
Mu-Hyun Baik
1985 ◽  
Vol 107 (13) ◽  
pp. 3855-3864 ◽  
Author(s):  
John A. Gilbert ◽  
Drake S. Eggleston ◽  
Wyatt R. Murphy ◽  
Daniel A. Geselowitz ◽  
Susan W. Gersten ◽  
...  

1985 ◽  
Vol 16 (42) ◽  
Author(s):  
J. A. GILBERT ◽  
D. S. EGGLESTON ◽  
W. R. JUN. MURPHY ◽  
D. A. GESELOWITZ ◽  
S. W. GERSTEN ◽  
...  

2012 ◽  
Vol 51 (3) ◽  
pp. 1345-1358 ◽  
Author(s):  
Jonah W. Jurss ◽  
Javier J. Concepcion ◽  
Jennifer M. Butler ◽  
Kristin M. Omberg ◽  
Luis M. Baraldo ◽  
...  

1981 ◽  
Vol 46 (5) ◽  
pp. 1237-1247
Author(s):  
Zdeněk Prokop ◽  
Karel Setínek

The catalyst containing redox sites in addition to acid functional groups was prepared by sulphonation of a macroporous chloromethylated styrene-divinylbenzene copolymer with concentrated sulphuric acid at elevated temperatures. Its activity was tested for the oxidation of 2-propanol by molecular oxygen at 120 °C and was found to be comparable to that of the iridium on carbon catalyst.Neutralisation of acid functional groups by alkali metal led to proportional decrease in the oxidation activity. The results of EPR spectroscopic study of these catalysts show that the redox properties of the polymer are caused by carbon clusters which are capable of electron exchange.


ACS Catalysis ◽  
2016 ◽  
Vol 6 (9) ◽  
pp. 5699-5705 ◽  
Author(s):  
Nagaraju Shilpa ◽  
Joydeb Manna ◽  
Parasmani Rajput ◽  
Rohit Kumar Rana

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