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Bound states charge-dipole interaction

Unlike molecular solvents, charge-dipole interaction cannot be expected between closed-shell atoms and excess electrons. However, finite and infinite ensembles of rare-gas atoms can support a bound and/or quasi-bound state for electrons, due solely to the collective polarization of the surrounding atoms. In bulk Xe, for instance, the conduction band lies 0.7 eV below the vacuum level [62]. The formation of negatively charged clusters has also been reported for He [35 37], Ne [38]... [Pg.3164]

Another type of interactions that can support an infinite number of bound states has an attractive dipole potential h2a/(2[zR2) asymptotically. Here, a is some constant, R is the distance between the centers of mass of the two subsystems which the whole system separates into, and /x is their reduced mass. Such an interaction occurs between a charged particle and a hydrogenlike atom in an excited state [59, 60]. [Pg.206]

The EDM r/e,p,nu of an electron, proton, or neutron is neccessarily aligned along the spin direction a of the particle. In essence, an EDM measurement in an atom or molecule involves polarizing the system with an applied external electric field and searching for the interaction E between the electronic or nuclear EDM and the polarized atom/molecule. Schiff s theorem [18] states that q = 0 if the atom/molecule is made of point particles bound by electrostatic forces. In other words, the electronic or nuclear EDM does not see the applied field because it is shielded out by the other charged particles. This theorem is important for its loopholes nuclei are not point particles and the electric dipole interaction is not screened when the electrons are relativistic. Consequently, q is not zero if the atom/molecule is well chosen [19,20]. Eor example the best measurement of the proton EDM comes from a measurement on TIE molecules [21], where the large size of the T1 nucleus ends up giving q 1 for the nuclear spin EDM interaction. The upper limit on the neutron EDM is known both directly, from measurements on free neutrons [22], and indirectly from nuclear spin measurements on Hg atoms [23]. [Pg.558]

M possesses a nonzero dipole moment, g. [If M has no dipole moment but a nonzero quadrupole moment, Q, then the asymptotic form of the potential is a charge-quadrupole interaction, V(r) -Q/r. ] The M -l-e potential well in Figure 4(a) is much shallower than that for M" " -l-e, consistent with the observation that IPs for neutral atoms and molecules are large compared to EAs. As such, the anion typically possesses few (if any) bound Rydberg states. ... [Pg.405]

The charge distribution in groups such as OH, NH and FH is very eccentric as far as the positive pole is concerned, that is to say, it can also be stated that the positive pole of the dipole lies externally, this in connection with the small size of the hydrogen atom bound as an ion (no electron cloud ). This gives rise to much stronger interaction than in other molecules with the same or even larger dipole moment. So much so that the complex of phenomena connected with this is discussed separately as the hydrogen bond ( 45). [Pg.333]

This energy depends on the interaction with the surroimding matter which results from electrical polarization, dipole orientation, van der Waals forees, and ehemical bond formation. Ligands strongly bound to a central ion or atom whieh remain connected with the redox species independent of its state of charge can be treated as a unit already existing in vacuum. For an illustration of the concepts, a polar liquid will be considered as the interacting medium. [Pg.46]


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See also in sourсe #XX -- [ Pg.225 ]




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