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Prasenjit Barman

Researcher at Indian Institute of Technology Guwahati

Publications -  12
Citations -  492

Prasenjit Barman is an academic researcher from Indian Institute of Technology Guwahati. The author has contributed to research in topics: Hydrogen atom abstraction & Reactivity (chemistry). The author has an hindex of 10, co-authored 11 publications receiving 413 citations.

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Long-Range Electron Transfer Triggers Mechanistic Differences between Iron(IV)-Oxo and Iron(IV)-Imido Oxidants

TL;DR: It is shown here that iron( IV)-tosylimido complex is much more reactive with sulfides than the corresponding iron(IV)-oxo complex; however, the reverse trend is obtained for hydrogen atom abstraction reactions.
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Comparison of the Reactivity of Nonheme Iron(IV)–Oxo versus Iron(IV)–Imido Complexes: Which is the Better Oxidant?†

TL;DR: The iron( IV)-imido variant reacts with sulfides five times faster than iron(IV)-oxo, whereas the reverse trend is observed for hydrogen atom abstraction.
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Deformylation Reaction by a Nonheme Manganese(III)-Peroxo Complex via Initial Hydrogen-Atom Abstraction.

TL;DR: Metal-peroxo intermediates are key species in the catalytic cycles of nonheme metalloenzymes, but their chemical properties and reactivity patterns are still poorly understood.
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Keto–Enol Tautomerization Triggers an Electrophilic Aldehyde Deformylation Reaction by a Nonheme Manganese(III)-Peroxo Complex

TL;DR: A combined spectroscopy, kinetics and computational study on aldehyde deformylation by two side-on manganese(III)-peroxo complexes with bispidine ligands finds a novel mechanism for the reaction that is initiated by a hydrogen atom abstraction reaction, which enables a keto-enol tautomerization in the substrate.
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Influence of ligand architecture on oxidation reactions by high-valent nonheme manganese oxo complexes using water as a source of oxygen.

TL;DR: Interestingly, one of the isomers of a bispidine ligand is significantly more reactive than the other (L(1) ), while in the corresponding Fe(IV)=O based oxidation reactions the L(2) -based system was previously found to be more reactivity than the L-based catalyst.