T
Tibor Bérces
Researcher at Hungarian Academy of Sciences
Publications - 124
Citations - 2903
Tibor Bérces is an academic researcher from Hungarian Academy of Sciences. The author has contributed to research in topics: Reaction rate constant & Excited state. The author has an hindex of 29, co-authored 124 publications receiving 2779 citations. Previous affiliations of Tibor Bérces include Centre national de la recherche scientifique.
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Journal ArticleDOI
IUPAC Critical Evaluation of Thermochemical Properties of Selected Radicals. Part I
Branko Ruscic,James E. Boggs,Alexander Burcat,Attila G. Császár,Jean Demaison,Rudolf Janoschek,Jan M. L. Martin,Melita L. Morton,Michel J. Rossi,John F. Stanton,Péter G. Szalay,Phillip R. Westmoreland,F. Zabel,Tibor Bérces +13 more
TL;DR: In this paper, the first part of a series of articles reporting critically evaluated thermochemical properties of selected free radicals is presented, including the enthalpy of formation, as well as the heat capacity, integrated heat capacity and entropy of the radicals.
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Spectroscopic properties of aromatic dicarboximides. Part1.—N—H and N-methyl-substituted naphthalimides
TL;DR: In this article, the photophysical properties of the N-H and N-methyl derivatives of 1,2-, 2,3- and 1,8-naphthalimides have been studied.
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Quenching Processes in Hydrogen-Bonded Pairs: Interactions of Excited Fluorenone with Alcohols and Phenols
TL;DR: In this paper, the authors studied the kinetics of dynamic quenching of singlet and triplet fluorenone by a series of alcohols, phenols, and related compounds, in which hydrogen-bonding power, redox potential, and acidity are systematically varied.
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Reaction rate analysis of complex kinetic systems
TL;DR: In this paper, a reaction rate sensitivity gradient is obtained, which is the derivative of the rate of species concentration change with respect to the rate coefficient, for high temperature formaldehyde oxidation and high-temperature propane pyrolysis.
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Comprehensive Model of the Photophysics of N-Phenylnaphthalimides: The Role of Solvent and Rotational Relaxation
TL;DR: In this article, the effects of substituents on the N-phenyl group on solvent polarity and viscosity have been studied, and a short-wavelength (SW) fluorescence, similar to the luminescence emitted by the n-alkyl derivatives, and/or a considerably red shifted long-wvelength (LW) luminecence are observed, and the ratio of the SW and LW fluorescence components is found to depend on substitution and on solvent properties.