Electronic current density induced by nuclear magnetic dipoles

1994 ◽  
Vol 313 (3) ◽  
pp. 299-304 ◽  
Author(s):  
P. Lazzeretti ◽  
M. Malagoli ◽  
R. Zanasi
1966 ◽  
Vol 145 (2) ◽  
pp. 507-518 ◽  
Author(s):  
H. Michael Gilder ◽  
David Lazarus

2018 ◽  
Author(s):  
Michihiro Okuyama ◽  
Fumihiko Sakata

<div>In studying a dynamical process of the chemical reaction, it is decisive to get appropriate information from an electronic current density. To this end, we divide one-body electronic density into a couple of densities, that is, an electronic sharing density and an electronic contraction density. Since the one-body electronic current density defi ned directly through the microscopic electronic wave function gives null value under the Born-Oppenheimer molecular dynamics, we propose to employ the Maxwell's displacement current density de fined by means of the one-body electronic density obtained under the same approximation. Applying the electronic sharing and the electronic contraction current densities to a hydrogen molecule, we show these densities give important physical quantities for analyzing a dynamical process of the covalent bond.</div>


1993 ◽  
Vol 48 (1-2) ◽  
pp. 134-136
Author(s):  
N. Sukumar ◽  
B. M. Deb ◽  
Harjinder Singh

Some consequences of the quantum fluid dynamics formulation are discussed for excited states of atoms and molecules and for time-dependent processes. It is shown that the conservation of electronic current density j(r) allows us to manufacture a gauge potential for each excited state of an atom, molecule or atom in a molecule. This potential gives rise to a tube of magnetic flux carried around by the many-electron system. In time-dependent situations, the evolution of the electronic density distribution can be followed with simple, site-dependent cellular automaton (CA) rules. The CA consists of a lattice of sites, each with a finite set of possible values, here representing finite localized elements of electronic charge and current density (since the charge density rno longer suffices to fully characterize a time-dependent system, it needs to be supplemented with information about the current density j).Our numerical results are presented elsewhere and further developmentis in progress.


1996 ◽  
Vol 74 (2) ◽  
pp. 185-200 ◽  
Author(s):  
T.A. Keith ◽  
R.F.W. Bader

This paper analyzes the nuclear magnetic shielding tensors underlying the chemical shift in NMR spectroscopy in terms of the field generated at the nucleus by the current J(1)(r) induced by an external magnetic field. The magnetic field at nucleus [Formula: see text] resulting from an element of the induced current density at a distance [Formula: see text] is proportional to [Formula: see text] which defines the shielding density [Formula: see text] The magnetic shielding of a nucleus is fundamentally an atomic property, a feature brought to the fore by using the theory of atoms in molecules and the integration of [Formula: see text] over the individual atomic basins relates the shielding tensor [Formula: see text] to a sum of atomic contributions. The shielding of nucleus ** is primarily determined by the flow of current within the basin of atom [Formula: see text], a contribution that varies from the approximate diamagnetic limit, given by the atomic Lamb value for the atom in the molecule, to values that are greatly reduced by the presence of paramagnetic current flows associated with particular bonding effects. Whether the contribution of a neighbouring atom is shielding or deshielding is readily understood by relating the form of the current flow within its basin to the magnetization density. [Formula: see text]. A study of the currents induced in benzene shows that the extent to which a proton, bonded to a ring of atoms, is deshielded by the field exerted by its bonded neighbour provides a direct diagnostic test for a ring current and an accurate relative measure of its strength. The theory of atoms in molecules isolates transferable atomic properties and because of this ability one finds, in addition to the anticipated result that a given functional group contributes identical amounts to the isotropic shielding [Formula: see text] of a nucleus external to it through a series of molecules, the more remarkable result that the whole of the variation in [Formula: see text] can have its origin in the basin of atom [Formula: see text], the contribution from external groups remaining constant. For example, the external contribution to [Formula: see text] for a carbon nucleus in a normal hydrocarbon is independent of chain length and position of [Formula: see text] within the chain, the methyl group in ethane contributing the same shielding to a methyl carbon as does the butyl group in pentane. This constancy in external contributions to the shielding is also found for N, O and F nuclei in substituted, saturated hydrocarbons. Key words: NMR, magnetic shielding, current density, magnetic shielding density.


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