Reply to the “Comment on ‘The Concept of Protobranching and Its Many Paradigm Shifting Implications for Energy Evaluations’”
Author:
Affiliation:
1. Center for Computational Chemistry and Department of Chemistry, University of Georgia, Athens, Georgia, 30602
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp909910f
Reference44 articles.
1. Ueber Polyacetylenverbindungen
2. Comment on “The Concept of Protobranching and Its Many Paradigm Shifting Implications for Energy Evaluations”
3. The Concept of Protobranching and Its Many Paradigm Shifting Implications for Energy Evaluations
4. All experimental data employed here are based on the experimental enthalpies of formation at 298 K given in the updated Sept. 2006 NIST CCCBDB Database (http://cccbdb.nist.gov/) and may differ slightly from earlier recommendations.
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4. Practical Tight-Binding Hückel-Like Modeling of Electronic Properties of Saturated Hydrocarbons: On σ-Aromaticity of Cyclopropane and Correlations of Alkane Ionization Energies and Enthalpies of Formation Corrected for Protobranching;The Journal of Physical Chemistry A;2018-07-30
5. Simultaneous Visualization of Covalent and Noncovalent Interactions Using Regions of Density Overlap;Journal of Chemical Theory and Computation;2014-07-11
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