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Prashant V. Kamat

Researcher at University of Notre Dame

Publications -  760
Citations -  86006

Prashant V. Kamat is an academic researcher from University of Notre Dame. The author has contributed to research in topics: Excited state & Racism. The author has an hindex of 140, co-authored 725 publications receiving 79259 citations. Previous affiliations of Prashant V. Kamat include Indian Institute of Technology Kanpur & Council of Scientific and Industrial Research.

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Photochemistry of squaraine dyes: excited states and reduced and oxidized forms of 4-(4-acetyl-3,5-dimethylpyrrolium-2-ylidene)-2-(4-acetyl-3,5-dimethylpyrrol-2-yl)-3-oxocyclobut-1-en-1-olate

TL;DR: The results of photoelectrochemical reduction of SQ in colloidal TiO2 suspension are also presented in this article, where the triplet excited states of SQ were characterized by both direct excitation (ϕT= 0.04, τs < 100 ps) and T-T sensitization models.
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Photocatalytic degradation of 4-chlorophenol : a mechanistically-based model

TL;DR: In this article, the photocatalytic degradation of 4-CP was mathematically modelled using the mechanistic insights and data presented in an earlier study, and the solution and surface concentrations of reacting species were calculated by solving a system of differential equations that account for oxidation reactions of dissolved and adsorbed species, adsorption and desorption, reduction of oxygen, and hole-electron recombination.
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Radical-induced oxidative transformation of quinoline

TL;DR: The primary events of the oxidative transformation of quinoline, an environmental pollutant, by different radicals have been investigated using pulse radiolysis in this paper, where the authors verified the possibility of the q-radical cation to undergo hydrolysis by generating the radical cation under laser induced photoionization conditions.
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Mechanistic pathways of the hydroxyl radical reactions of quinoline. 2. Computational analysis of hydroxyl radical attack at C atoms.

TL;DR: The computational analysis of the energy surface for the reaction of *OH with quinoline reveals that the formation of OH adducts proceeds through exothermic formation of pi-complexes/H-bonded complexes.