Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Quantum mechanics symmetry

Nuclei with spin I > are not, as a rule, perfectly spherical distributions of charge, as may be shown by quite general quantum mechanical symmetry considerations (89). All nuclei possess the spin axis as a sym-... [Pg.53]

In Section 10.4 we studied projective unitary representations, important because they are symmetries of quantum systems. It is natural to wonder whether projective unitary symmetries are the only symmetries of quantum systems. In this section, we will show that complex conjugation, while not projective unitary, is a physical symmetry, i.e., it preserves all the physically relevant quantities. The good news is that complex conjugation is essentially the only physical symmetry we missed. More precisely, each physical symmetry is either projective unitary or it is the composition of a projective unitary symmetry with complex conjugation. This result (Proposition 10.10) is known as Wigner s theorem on quantum mechanical symmetries. The original proof can be found in the appendix to Chapter 20 in Wigner s book [Wi]. [Pg.323]

Chemical mechanisms for l60 enrichment It was discovered in the lab, in molecular clouds and in the Earth s atmosphere that purely chemical processes exist that can enrich only l60, leaving the ratio 170/l80 unchanged. This is observed in the formation of ozone. Itis understood by quantum mechanical symmetries, in which the ozone l60-l60-l60 is more symmetrical than either 170-l60-l60 or l80-l60-l60 and therefore has different numbers of quantum transition states. [Pg.91]

W. Greiner and B. Muller, Quantum Mechanics. Symmetries, 2nd. ed., 1994, Springer, Heidelberg. [Pg.257]

Figure 3.5 Charge penetration in base stacking for the GGiCC base pair step [at 35° Twist and 0.28 A Siide] as a function of Rise, the vertical separation between the base pairs. The difference between the distributed multipole analysis [DMA) value for electrostatics and the quantum mechanical symmetry-adapted perturbation theory [SAPTO/jun-cc-pVDZ) value for electrostatics may be taken as a measure of the charge penetration term. The DMA analysis includes terms up through order 5 [32pole-chai e, hexadecapole-dipole, octopole-quadrupole). Charge penetration rapidly increases in magnitude for smaller intermolecular distances. Figure 3.5 Charge penetration in base stacking for the GGiCC base pair step [at 35° Twist and 0.28 A Siide] as a function of Rise, the vertical separation between the base pairs. The difference between the distributed multipole analysis [DMA) value for electrostatics and the quantum mechanical symmetry-adapted perturbation theory [SAPTO/jun-cc-pVDZ) value for electrostatics may be taken as a measure of the charge penetration term. The DMA analysis includes terms up through order 5 [32pole-chai e, hexadecapole-dipole, octopole-quadrupole). Charge penetration rapidly increases in magnitude for smaller intermolecular distances.
Wave function, 10, 108, 370. See also Quantum mechanics symmetry, 127 WebLab Viewer, 351 Weiner index, 245... [Pg.1]

Since it is not possible to generate antisynnnetric combinations of products if the same spin orbital appears twice in each tenn, it follows that states which assign the same set of four quantum numbers twice cannot possibly satisfy the requirement P.j i = -ij/, so this statement of the exclusion principle is consistent with the more general symmetry requirement. An even more general statement of the exclusion principle, which can be regarded as an additional postulate of quantum mechanics, is... [Pg.30]

At this point the reader may feel that we have done little in the way of explaining molecular synnnetry. All we have done is to state basic results, nonnally treated in introductory courses on quantum mechanics, connected with the fact that it is possible to find a complete set of simultaneous eigenfiinctions for two or more commuting operators. However, as we shall see in section Al.4.3.2. the fact that the molecular Hamiltonian //coimmites with and F is intimately coimected to the fact that //commutes with (or, equivalently, is invariant to) any rotation of the molecule about a space-fixed axis passing tlirough the centre of mass of the molecule. As stated above, an operation that leaves the Hamiltonian invariant is a symmetry operation of the Hamiltonian. The infinite set of all possible rotations of the... [Pg.140]

The origin of a torsional barrier can be studied best in simple cases like ethane. Here, rotation about the central carbon-carbon bond results in three staggered and three eclipsed stationary points on the potential energy surface, at least when symmetry considerations are not taken into account. Quantum mechanically, the barrier of rotation is explained by anti-bonding interactions between the hydrogens attached to different carbon atoms. These interactions are small when the conformation of ethane is staggered, and reach a maximum value when the molecule approaches an eclipsed geometry. [Pg.343]

Essentially all of the model problems that have been introduced in this Chapter to illustrate the application of quantum mechanics constitute widely used, highly successful starting-point models for important chemical phenomena. As such, it is important that students retain working knowledge of the energy levels, wavefunctions, and symmetries that pertain to these models. [Pg.55]

M. Tinkham, Group Theory and Quantum Mechanics McGraw-Hill, New York (1964). R. McWeeny, Symmetry An Introduction to Group Theory and its Applications Pergamon, New York (1963). [Pg.127]

The fourth quantum number is called the spin angular momentum quantum number for historical reasons. In relativistic (four-dimensional) quantum mechanics this quantum number is associated with the property of symmetry of the wave function and it can take on one of two values designated as -t-i and — j, or simply a and All electrons in atoms can be described by means of these four quantum numbers and, as first enumerated by W. Pauli in his Exclusion Principle (1926), each electron in an atom must have a unique set of the four quantum numbers. [Pg.22]

The subset 0kv 0k2> 0k3,. . . formed from the complete set by means of the projection operator 0k is called /l-adapted or symmetry-adapted in the case when A is a symmetry operator. From Eqs. III.81 and III.86 it follows that the projection operators 0k commute with H and, using this property, the quantum-mechanical turn-over rule/ and Eq. III.91, we obtain... [Pg.288]

Relationship Between Physical Transformations and Quantum Mechanical Operators.—In order to obtain information concerning the symmetry... [Pg.726]

Strictly, L is defined only as a quantum number for a spherical environment - the free ion. The use of L ff = 0 for A terms or Leff = 1 for L terms on the grounds that (2Leff + 1) equals the degeneracy of these terms is, however, legitimate as used here. There is a close parallel between the quantum mechanics of T terms in octahedral or tetrahedral symmetry on the one hand, and of P terms in spherical symmetry on the other. [Pg.88]

The relationship between spin and the symmetry character of the wave function can be established in relativistic quantum theory. In non-relativistic quantum mechanics, however, this relationship must be regarded as a postulate. [Pg.217]


See other pages where Quantum mechanics symmetry is mentioned: [Pg.799]    [Pg.640]    [Pg.640]    [Pg.140]    [Pg.99]    [Pg.799]    [Pg.640]    [Pg.640]    [Pg.140]    [Pg.99]    [Pg.16]    [Pg.137]    [Pg.454]    [Pg.386]    [Pg.46]    [Pg.208]    [Pg.4]    [Pg.149]    [Pg.445]    [Pg.397]    [Pg.857]    [Pg.691]    [Pg.275]    [Pg.13]    [Pg.106]    [Pg.209]    [Pg.249]    [Pg.249]    [Pg.502]    [Pg.725]    [Pg.728]    [Pg.763]    [Pg.117]    [Pg.329]    [Pg.767]    [Pg.76]    [Pg.146]    [Pg.55]   
See also in sourсe #XX -- [ Pg.178 ]

See also in sourсe #XX -- [ Pg.4 , Pg.5 , Pg.40 ]




SEARCH



Introduction to Symmetry in Quantum Mechanics

© 2024 chempedia.info