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Halogen bonding: an electrostatically-driven highly directional noncovalent interaction
P. Politzer, J. Murray, Tim Clark
School of Pharmacy & Biomedical Sciences
Research output
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peer-review
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INIS
holes
100%
halogens
100%
bonding
80%
interactions
60%
atoms
60%
electrostatics
40%
surfaces
20%
surveys
20%
hydrogen
20%
molecules
20%
crystallography
20%
electrons
20%
potentials
20%
chemical bonds
20%
lewis bases
20%
Chemistry
Halogen
100%
Atom
60%
Electrostatic Potential
40%
Chemical Bond
40%
R
40%
Crystal Structure
20%
Pi Electron
20%
Nucleophile
20%
Electrophile
20%
Lewis Base
20%
Group
20%
Molecule
20%
Surface
20%
Intravenous
20%
Hydrogen Bonding
20%
Orbital
20%
Covalent Modification
20%
Pharmacology, Toxicology and Pharmaceutical Science
Halogen
80%
Hydrogen
20%
Halogen Bond
20%
Lewis Base
20%
Covalent Bond
20%
Nucleophile
20%
Electrophile
20%