Amino acids form strongly bound anions when substituted with superhalogen ligands
Author:
Publisher
AIP Publishing
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://aip.scitation.org/doi/pdf/10.1063/1.4798320
Reference32 articles.
1. On the Number of Water Molecules Necessary To Stabilize the Glycine Zwitterion
2. Dipole-Bound Anions of Glycine Based on the Zwitterion and Neutral Structures
3. Quasidegeneracy of Zwitterionic and Canonical Tautomers of Arginine Solvated by an Excess Electron
4. Zwitterion formation in hydrated amino acid, dipole bound anions: How many water molecules are required?
5. Preparation and photoelectron spectrum of the glycine molecular anion: Assignment to a dipole-bound electron species with a high-dipole moment, non-zwitterionic form of the neutral core
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1. Electron Propagator Theory of Vertical Electron Detachment Energies of Anions: Benchmarks and Applications to Nucleotides;J PHYS CHEM A;2023
2. Electron Propagator Theory of Vertical Electron Detachment Energies of Anions: Benchmarks and Applications to Nucleotides;The Journal of Physical Chemistry A;2023-01-19
3. Assessment of XC functionals for the study of organic molecules with superhalogen substitution. A systematic comparison between DFT and CCSD(T);The Journal of Chemical Physics;2022-05-14
4. Electron affinity of modified benzene;International Journal of Quantum Chemistry;2017-09-28
5. Comparative study of hydrogenated and lithiated superhalogens;Chemical Physics Letters;2016-09
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