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Electron-nuclear interaction

In this presentation, the monoatomic terms of the Hamiltonian contain only one-center integrals and the diatomic terms contain one- and two-center ones. While the first few terms in Eq. (34) describe direct diatomic interactions (electron-nuclear and electron-electron), most of the terms contain differences between a two-center integral related to mtraatomic interactions and its approximation by one-center integrals and projection-related matrices A, Uke the term... [Pg.41]

This gives the total energy, which is also the kinetic energy in this case because the potential energy is zero within the box , m tenns of the electron density p x,y,z) = (NIL ). It therefore may be plausible to express kinetic energies in tenns of electron densities p(r), but it is by no means clear how to do so for real atoms and molecules with electron-nuclear and electron-electron interactions operative. [Pg.2181]

Here, t is the nuclear kinetic energy operator, and so all terms describing the electronic kinetic energy, electron-electron and electron-nuclear interactions, as well as the nuclear-nuclear interaction potential function, are collected together. This sum of terms is often called the clamped nuclei Hamiltonian as it describes the electrons moving around the nuclei at a particular configrrration R. [Pg.257]

DFT methods compute electron correlation via general functionals of the electron density (see Appendix A for details). DFT functionals partition the electronic energy into several components which are computed separately the kinetic energy, the electron-nuclear interaction, the Coulomb repulsion, and an exchange-correlation term accounting for the remainder of the electron-electron interaction (which is itself... [Pg.118]

Hfi includes a nuclear Zeeman term, a nuclear dipole-dipole term, an electron-nuclear dipole term and a term describing the interaction between the nuclear dipole and the electron orbital motion. [Pg.308]

The origin of postulate (iii) lies in the electron-nuclear hyperfine interaction. If the energy separation between the T and S states of the radical pair is of the same order of magnitude as then the hyperfine interaction can represent a driving force for T-S mixing and this depends on the nuclear spin state. Only a relatively small preference for one spin-state compared with the other is necessary in the T-S mixing process in order to overcome the Boltzmann polarization (1 in 10 ). The effect is to make n.m.r. spectroscopy a much more sensitive technique in systems displaying CIDNP than in systems where only Boltzmann distributions of nuclear spin states obtain. More detailed consideration of postulate (iii) is deferred until Section II,D. [Pg.58]

Here and H describe radicals A and B of the radical pair and He the interaction of their electrons. The other terms in equation (15) are H g, the spin orbit coupling term, H g and Hgj, representing the interaction of the externally applied magnetic field with the electron spin and nuclear spin, respectively Hgg is the electron spin-spin interaction and Hgi the electron-nuclear hyperfine interaction. [Pg.69]

OIDEP usually results from Tq-S mixing in radical pairs, although T i-S mixing has also been considered (Atkins et al., 1971, 1973). The time development of electron-spin state populations is a function of the electron Zeeman interaction, the electron-nuclear hyperfine interaction, the electron-electron exchange interaction, together with spin-rotational and orientation dependent terms (Pedersen and Freed, 1972). Electron spin lattice relaxation Ti = 10 to 10 sec) is normally slower than the polarizing process. [Pg.121]

The most stable shape for any molecule maximizes electron-nuclear attractive interactions while minimizing nuclear-nuclear and electron-electron repulsions. The distribution of electron density in each chemical bond is the result of attractions between the electrons and the nuclei. The distribution of chemical bonds relative to one another, on the other hand, is dictated by electrical repulsion between electrons in different bonds. The spatial arrangement of bonds must minimize electron-electron repulsion. This is accomplished by keeping chemical bonds as far apart as possible. The principle of minimizing electron-electron repulsion is called valence shell electron pair repulsion, usually abbreviated VSEPR. [Pg.604]

The individual terms in (5.2) and (5.3) represent the nuclear-nuclear repulsion, the electronic kinetic energy, the electron-nuclear attraction, and the electron-electron repulsion, respectively. Thus, the BO Hamiltonian is of treacherous simplicity it merely contains the pairwise electrostatic interactions between the charged particles together with the kinetic energy of the electrons. Yet, the BO Hamiltonian provides a highly accurate description of molecules. Unless very heavy elements are involved, the exact solutions of the BO Hamiltonian allows for the prediction of molecular phenomena with spectroscopic accuracy that is... [Pg.139]

We now need to discuss how these contributions that are required to construct the Kohn-Sham matrix are determined. The fust two terms in the parenthesis of equation (7-12) describe the electronic kinetic energy and the electron-nuclear interaction, both of which depend on the coordinate of only one electron. They are often combined into a single integral, i. e ... [Pg.112]

Although following similar nuclear reaction schemes, nuclear analytical methods (NAMs) comprise bulk analysing capability (neutron and photon activation analysis, NAA and PAA, respectively), as well as detection power in near-surface regions of solids (ion-beam analysis, IB A). NAMs aiming at the determination of elements are based on the interaction of nuclear particles with atomic nuclei. They are nuclide specific in most cases. As the electronic shell of the atom does not participate in the principal physical process, the chemical bonding status of the element is of no relevance. The general scheme of a nuclear interaction is ... [Pg.662]

In the latter expression, V(r,) is the electron-nuclear attraction operator describing the interaction of the z th electron of the molecule with the set of nuclei. [Pg.67]

In Equation (6) ge is the electronic g tensor, yn is the nuclear g factor (dimensionless), fln is the nuclear magneton in erg/G (or J/T), In is the nuclear spin angular momentum operator, An is the electron-nuclear hyperfine tensor in Hz, and Qn (non-zero for fn > 1) is the quadrupole interaction tensor in Hz. The first two terms in the Hamiltonian are the electron and nuclear Zeeman interactions, respectively the third term is the electron-nuclear hyperfine interaction and the last term is the nuclear quadrupole interaction. For the usual systems with an odd number of unpaired electrons, the transition moment is finite only for a magnetic dipole moment operator oriented perpendicular to the static magnetic field direction. In an ESR resonator in which the sample is placed, the microwave magnetic field must be therefore perpendicular to the external static magnetic field. The selection rules for the electron spin transitions are given in Equation (7)... [Pg.505]

The physical interpretation of the anisotropic principal values is based on the classical magnetic dipole interaction between the electron and nuclear spin angular momenta, and depends on the electron-nuclear distance, rn. Assuming that both spins can be described as point dipoles, the interaction energy is given by Equation (8), where 6 is the angle between the external magnetic field and the direction of rn. [Pg.506]

An exception to this rule arises in the ESR spectra of radicals with small hyperfine parameters in solids. In that case the interplay between the Zeeman and anisotropic hyperfine interaction may give rise to satellite peaks for some radical orientations (S. M. Blinder, J. Chem. Phys., 1960, 33, 748 H. Sternlicht,./. Chem. Phys., 1960, 33, 1128). Such effects have been observed in organic free radicals (H. M. McConnell, C. Heller, T. Cole and R. W. Fessenden, J. Am. Chem. Soc., 1959, 82, 766) but are assumed to be negligible for the analysis of powder spectra (see Chapter 4) where A is often large or the resolution is insufficient to reveal subtle spectral features. The nuclear Zeeman interaction does, however, play a central role in electron-nuclear double resonance experiments and related methods [Appendix 2 and Section 2.6 (Chapter 2)]. [Pg.6]

S. Sinnecker, E. Reijerse, F. Neese and W. Lubitz, Hydrogen bond geometries from paramagnetic resonance and electron-nuclear double resonance parameters Density functional study of quinone radical anion-solvent interactions, J. Am. Chem. Soc., 2004, 126, 3280. [Pg.166]

An indirect mode of anisotropic hyperfine interaction arises as a result of strong spin-orbit interaction (174)- Nuclear and electron spin magnetic moments are coupled to each other because both are coupled to the orbital magnetic moment. The Hamiltonian is... [Pg.339]

Electron nuclear dynamics theory is a direct nonadiabatic dynamics approach to molecular processes and uses an electronic basis of atomic orbitals attached to dynamical centers, whose positions and momenta are dynamical variables. Although computationally intensive, this approach is general and has a systematic hierarchy of approximations when applied in an ab initio fashion. It can also be applied with semiempirical treatment of electronic degrees of freedom [4]. It is important to recognize that the reactants in this approach are not forced to follow a certain reaction path but for a given set of initial conditions the entire system evolves in time in a completely dynamical manner dictated by the interparticle interactions. [Pg.327]

Chemistry is the science that deals with the interaction between different forms of matter to bring about a change in the nature of the interacting matter. According to the nuclear model of the atom it is evident that chemical interaction is due to interacting electron clouds. In order to understand chemical interactions it is therefore necessary to understand, in the first place the behaviour of electrons. [Pg.97]


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See also in sourсe #XX -- [ Pg.47 , Pg.98 ]

See also in sourсe #XX -- [ Pg.512 , Pg.513 , Pg.514 , Pg.515 , Pg.516 , Pg.517 ]




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Dipolar interaction electron-nuclear

ESEEM weak electron-nuclear hyperfine interaction

Electron nuclear dipolar interaction distances

Electron nuclear double resonance hyperfine interactions

Electron nuclear spin interaction energy

Electron orbit-nuclear spin interaction

Electron spin resonance spectroscopy nuclear hyperfine interaction

Electronic interactions

Electronic interactions in the nuclear Hamiltonian

Interaction of a nuclear magnetic moment with an electron shell

Intraatomic Electron-Nuclear Interactions

Minimum energy coordinates electronic-nuclear interaction

Nuclear hyperfine interactions, electron

Nuclear hyperfine interactions, electron paramagnetic resonance

Nuclear interaction

Nuclear spin, electron quadrupole interaction

Zeeman interaction electron-nuclear double resonance

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