The problem of the binding of an excess electron to polar molecules and their clusters has long fascinated researchers. Although excess electrons bound to such species tend to be very extended spatially and to have little spatial overlap with the valence electrons of the neutral molecules, inclusion of electron correlation effects is essential for quantitatively describing the electron binding. The major electron correlation contribution may be viewed as a dispersion interaction between the excess electron and the electrons of the molecule or cluster. Recent work using a one-electron Drude model to describe excess electrons interacting with polar molecules is reviewed.\ud \u
Any molecule with a dipole moment above approximately 2.5 Debye can form a stable negative ion (dipo...
Electron localization is studied in formamide cluster anions. The isolated formamide molecule has a...
The Drude model for treating the interaction of excess electrons with polar molecules is extended to...
The problem of the binding of an excess electron to polar molecules and their clusters has long fasc...
The problem of the binding of an excess electron to polar molecules and their clusters has long fasc...
The problem of the binding of an excess electron to polar molecules and their clusters with sufficie...
A model potential approach used to study the interactions between an excess electron and polar molec...
In this work we focus on the binding of excess electrons to water clusters, a problem for which disp...
Electron attachment properties of covalent molecules and ion clusters with vanishing dipole moments ...
In this work we focus on the binding of excess electrons to water clusters, a problem for which disp...
Thermal energy electron attachment to closed-shell homogeneous polar cluster is reviewed. Different ...
An excess electron can be bound to a molecule in a very diffuse orbital as a result of the long-rang...
A one-electron model potential approach for calculating the binding energies of an excess electron\u...
Any molecule with a dipole moment above approximately 2.5 Debye can form a stable negative ion (dipo...
A one-electron model potential approach for calculating the binding energies of an excess electron\u...
Any molecule with a dipole moment above approximately 2.5 Debye can form a stable negative ion (dipo...
Electron localization is studied in formamide cluster anions. The isolated formamide molecule has a...
The Drude model for treating the interaction of excess electrons with polar molecules is extended to...
The problem of the binding of an excess electron to polar molecules and their clusters has long fasc...
The problem of the binding of an excess electron to polar molecules and their clusters has long fasc...
The problem of the binding of an excess electron to polar molecules and their clusters with sufficie...
A model potential approach used to study the interactions between an excess electron and polar molec...
In this work we focus on the binding of excess electrons to water clusters, a problem for which disp...
Electron attachment properties of covalent molecules and ion clusters with vanishing dipole moments ...
In this work we focus on the binding of excess electrons to water clusters, a problem for which disp...
Thermal energy electron attachment to closed-shell homogeneous polar cluster is reviewed. Different ...
An excess electron can be bound to a molecule in a very diffuse orbital as a result of the long-rang...
A one-electron model potential approach for calculating the binding energies of an excess electron\u...
Any molecule with a dipole moment above approximately 2.5 Debye can form a stable negative ion (dipo...
A one-electron model potential approach for calculating the binding energies of an excess electron\u...
Any molecule with a dipole moment above approximately 2.5 Debye can form a stable negative ion (dipo...
Electron localization is studied in formamide cluster anions. The isolated formamide molecule has a...
The Drude model for treating the interaction of excess electrons with polar molecules is extended to...