Electron Attachment to the Hydrogenated Watson−Crick Guanine Cytosine Base Pair (GC+H): Conventional and Proton-Transferred Structures
Author:
Affiliation:
1. Center for Computational Chemistry and Department of Chemistry, University of Georgia, Athens, GA 30602-2525
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp711958p
Reference72 articles.
1. Elucidation of Primary Radiation Damage in DNA through Application ofAb InitioMolecular Orbital Theory
2. Purine bases, nucleosides, and nucleotides: aqueous solution redox chemistry and transformation reactions of their radical cations and e- and OH adducts
3. One-electron-reduction potentials of pyrimidine bases, nucleosides, and nucleotides in aqueous solution. Consequences for DNA redox chemistry
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2. Experimental and theoretical assessment of protonated Hoogsteen 9-methylguanine–1-methylcytosine base-pair dissociation: kinetics within a statistical reaction framework;Physical Chemistry Chemical Physics;2021
3. Density functional theory studies on cytosine analogues for inducing double-proton transfer with guanine;Scientific Reports;2020-06-15
4. Is non-statistical dissociation a general feature of guanine–cytosine base-pair ions? Collision-induced dissociation of a protonated 9-methylguanine–1-methylcytosine Watson–Crick base pair, and comparison with its deprotonated and radical cation analogues;Physical Chemistry Chemical Physics;2020
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