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Polarisation atoms

For isolated atoms, the polarisability is isotropic - it does not depend on the orientation of fhe atom with respect to the applied field, and the induced dipole is in the direction of the electric field, as in Equation (4.51). However, the polarisability of a molecule is often anisotropic. This means that the orientation of the induced dipole is not necessarily in the same direction as the electric field. The polarisability of a molecule is often modelled as a collection of isotropically polarisable atoms. A small molecule may alternatively be modelled as a single isotropic polarisable centre. [Pg.217]

These groups, and other such as S03H, CN, COR, etc., all have in common a positively charged, or positively polarised, atom adjacent to a carbon atom of the benzene ring ... [Pg.151]

Debye interaction occurs when a permanent dipole induces a dipole in a polarisable atom or molecule. The induced dipole is oriented in such a way that attraction occurs. [Pg.40]

The preparation of spin-polarised atomic beams began with the pioneering work of Gerlach and Stern (1924). It was extensively developed in the 1950s during studies of the hyperfine structure of atoms (Ramsey, 1956) and later by nuclear physicists who were interested in the study of the spin dependence of nuclear forces. [Pg.39]

Fig. 2.18 Basic scheme for the production of a spin-polarised atomic beam. Fig. 2.18 Basic scheme for the production of a spin-polarised atomic beam.
Fig. 2.22. Schematic of the polarised electron—polarised atom scattering apparatus of McClelland et al. (1986, 1989). Fig. 2.22. Schematic of the polarised electron—polarised atom scattering apparatus of McClelland et al. (1986, 1989).
The all-electron partial waves, i, are chosen to be solutions of the scalar relativistic Schrodinger equation for a non-spin-polarised atom with a specific angular... [Pg.126]

The anion is protonated on the carbon end to give rise to a linear molecule, HCN, which is called hydrogen cyanide or hydrocyanic acid. A reagent that has lone pairs on two or more different atoms with which it may attack another compound is called ambident. The atom that attacks depends upon the nature of the atomic centre that it is being attacked. In the case of protonation, the hard, less easily polarised, atom reacts with the proton, which is itself a hard species. This type of interaction will be studied in more detail in Chapter 7. [Pg.69]

At the end of the chemistry course the students are familiar with the fundamentals of chemical bonding, can differentiate between atomic bonds including polarised atomic bonds, ionic bonds and metallic bonds. They can relate the kind of bond to the property of the substance and are familiar with the structure and phenomenon of substances. They can also workout relationship between the structure and the reaction of organic substances. Chemistry imparts basic knowledge about major industries. Students also acquire knowledge about application of chemical science in other branches of production and spheres of life as well as about the inter-relationship between chemical industry and other industries. In the process they also realise the need of applying chemistry to well being of mankind. [Pg.166]

Polarisability of the heteroatom. More polarisable atoms, such as sulfur, are able to disperse charge more effectively. [Pg.38]

On the experimental side much more numerous and more accurate data are required. It will be necessary to know with exactitude how Z>, Dq and E in the expression D = vary with composition in alloy systems. Many more selfdiffusion coefficients obtained by the radioactive indicator method are required. The connections between polarisation, atomic radius and density, position in the periodic table, alloy formation, melting-point, and degree of lattice loosening must be placed upon a more quantitative basis than the present data permit. When these properties have been correlated among themselves, and with existing X-ray data on crystal structure, it should be possible to understand more clearly phenomena of diffusion in metallic and non-metallic lattices. [Pg.304]

Campbell, E. E. B. and R. D. Levine (2000). Delayed ionization and fragmentation en route to thermionic emission statistics and dynamics. Ann. Rev. Phys. Chem. 51, 65. Campbell, E. E. B., H. Schmidt, et al. (1988). Symmetry and angular momentum in collisions with laser excited polarised atoms. ylrfu Chem. Phys. 72, 37. [Pg.506]


See other pages where Polarisation atoms is mentioned: [Pg.218]    [Pg.98]    [Pg.38]    [Pg.98]    [Pg.55]    [Pg.55]    [Pg.70]    [Pg.558]    [Pg.184]    [Pg.128]    [Pg.39]    [Pg.39]    [Pg.40]    [Pg.41]    [Pg.43]    [Pg.199]    [Pg.244]    [Pg.36]    [Pg.524]    [Pg.200]    [Pg.364]    [Pg.149]    [Pg.195]    [Pg.301]    [Pg.229]   
See also in sourсe #XX -- [ Pg.39 , Pg.40 , Pg.41 , Pg.42 , Pg.43 , Pg.44 ]




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Polarisability

Polarisable

Polarisation

Polarisation atomic

Polarisation atomic

Polarised atoms

Polarised atoms

Polarised atoms analysis

Polarised atoms sources

Polariser

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