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Debabrata Chatterjee

Researcher at Central Mechanical Engineering Research Institute

Publications -  100
Citations -  2903

Debabrata Chatterjee is an academic researcher from Central Mechanical Engineering Research Institute. The author has contributed to research in topics: Catalysis & Ruthenium. The author has an hindex of 23, co-authored 96 publications receiving 2666 citations. Previous affiliations of Debabrata Chatterjee include University of Burdwan & Centre national de la recherche scientifique.

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Electrochemistry of Ru(edta) complexes relevant to small molecule transformations: Catalytic implications and challenges

TL;DR: In this paper, results of the electrochemical studies of both mononuclear and binuclear complexes of Ru(edta) are reviewed with regard to electron-transfer reaction mechanism and activity, highlighting their potential to act as redox mediators or catalysts in electrochemical transformations of small molecules and enzymatic reactions.
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Electrochemical Conversion of Bicarbonate to Formate Mediated by the Complex RuIII(edta) (edta4– = ethylenediaminetetraacetate)

TL;DR: In this article, the first example of a ruthenium(III) complex, [RuIII(edta)] (edta = ethylenediaminetetraacetate), that catalyzes the electrochemical conversion of hydrogen carbonate to formate selectively was presented.
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RuIII(edta) mediated oxidation of azide in the presence of hydrogen peroxide. Azide versus peroxide activation

TL;DR: The kinetics of the catalytic oxidation process was studied by using stopped-flow and rapid-scan spectrophotometry as a function of [Ru(III)(edta)], [H2O2], [N3(-)] and pH and detailed reaction mechanisms in agreement with the spectroscopic and kinetic data are presented.
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Substrate versus oxidant activation in RuIII(edta) catalyzed dye degradation

TL;DR: In this paper, the catalytic degradation of methylene blue (MB) in the presence of H2O2 has been achieved within 300 s. Complete degradation of 0.05 mM MB was noticed within 300 seconds in the case of 5.0 μM of Ru(edta) catalyst under ambient conditions.
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Reactivity of [RuIII(pac)(H2O)] (pac = polyaminocarboxylate) complexes with 5′-nucleotides and their antitumor activity

TL;DR: Kinetic results suggest that the binding of 5′-nucleotides takes place in a rapid [Nu] dependent rate-determining step and is accounted for the operation of an associative mechanism.