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Quantitative resonance-based mechanistic analysis for modern chemical reaction pathways
Traditional arrow-pushing models offer qualitative intuition but lack quantitative rigor for describing electronic rearrangements in chemical reactions. Natural Resonance Theory of Chemical Reaction Mechanisms applies modern NRT methodology, built on the Natural Bond Orbital framework, to derive detailed electronic mechanisms along full reaction pathways using Pauling-type resonance conceptions grounded in first-principles quantum chemical calculations.
The book systematically covers NRT theoretical foundations, computational implementation in programs such as Gaussian, GAMESS, and ORCA, and applications spanning organic, inorganic, radical, and transition-state processes. Readers gain quantitative tools for assessing resonance weights, bond orders, valency, and bond polarity across classic reactions of the synthetic literature.
The book also provides:
Researchers and practitioners in chemistry, biochemistry, molecular physics, and pharmacy will find this book an authoritative reference for NRT-based mechanistic analysis. Upper-level undergraduate and graduate students seeking rigorous, quantitative approaches to electronic reaction mechanisms will also benefit from its systematic treatment.
Quantitative resonance-based mechanistic analysis for modern chemical reaction pathways
Traditional arrow-pushing models offer qualitative intuition but lack quantitative rigor for describing electronic rearrangements in chemical reactions. Natural Resonance Theory of Chemical Reaction Mechanisms applies modern NRT methodology, built on the Natural Bond Orbital framework, to derive detailed electronic mechanisms along full reaction pathways using Pauling-type resonance conceptions grounded in first-principles quantum chemical calculations.
The book systematically covers NRT theoretical foundations, computational implementation in programs such as Gaussian, GAMESS, and ORCA, and applications spanning organic, inorganic, radical, and transition-state processes. Readers gain quantitative tools for assessing resonance weights, bond orders, valency, and bond polarity across classic reactions of the synthetic literature.
The book also provides:
Researchers and practitioners in chemistry, biochemistry, molecular physics, and pharmacy will find this book an authoritative reference for NRT-based mechanistic analysis. Upper-level undergraduate and graduate students seeking rigorous, quantitative approaches to electronic reaction mechanisms will also benefit from its systematic treatment.
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