Journal
JOURNAL OF PHYSICAL CHEMISTRY A
Volume 125, Issue 9, Pages 1927-1940Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpca.1c00183
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Funding
- ETH Zurich
- Swiss National Science Foundation
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This study explores the comparison of performance between conventional rate models and L-CID model within the RRKM framework, showing that the BDE values obtained with L-CID model are consistent with those from other rate models within expected uncertainty bounds based on analysis of microcanonical rate data and reaction cross-section data.
The Rice-Ramsperger-Kassel-Marcus (RRKM) theory provides a simple yet powerful rate theory for calculating microcanonical rate constants. In particular, it has found widespread use in combination with gas-phase kinetic experiments of unimolecular dissociations to extract experimental bond dissociation energies (BDEs). We have previously found several discrepancies between the computed BDE values and the respective experimental ones, obtained with our empirical rate model, named L-CID. To investigate the reliability of our rate model, we conducted a theoretical analysis and comparison of the performance of conventional rate models and L-CID within the RRKM framework. Using the previously published microcanonical rate data as well as reaction cross-section data, we show that the BDE values obtained with the L-CID model agree with the ones from the other rate models within the expected uncertainty bounds. Based on this agreement, we discuss the possible rationalization of the good performance of the L-CID model.
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