Angular momentum described

The simplest case arises when the electronic motion can be considered in temis of just one electron for example, in hydrogen or alkali metal atoms. That electron will have various values of orbital angular momentum described by a quantum number /. It also has a spin angular momentum described by a spin quantum number s of d, and a total angular momentum which is the vector sum of orbital and spin parts with... 

Fig. 5.15. Evolution of giant resonances as the binding energy of the short-range inner well becomes progressively smaller (a) according to Hartree-Fock calculations due to Combet-Farnoux and (b) according to the spherical square well with angular momentum described in the text (after J.-P. Connerade [222]).

In the basis sets discussed so far, we have included only orbitals of the same symmetries as those of the occupied AOs. However, because of the lower symmetry of molecules compared with that of their constituent atoms, functions of symmetry different from those of the occupied orbitals can contribute to the Hartree-Fock wave function. For instance, in a diatomic molecule, the a component of the 2p orbitals can contribute to the occupied log orbital. These functions of higher angular momentum describe the polarization of the charge distribution upon formation of a chemical bond. To see the polarizing effect of such functions, let (A) be a GTO positioned at A ... 

We have described here one particular type of molecular synnnetry, rotational symmetry. On one hand, this example is complicated because the appropriate symmetry group, K (spatial), has infinitely many elements. On the other hand, it is simple because each irreducible representation of K (spatial) corresponds to a particular value of the quantum number F which is associated with a physically observable quantity, the angular momentum. Below we describe other types of molecular synnnetry, some of which give rise to finite synnnetry groups. 

The anisotropy of the product rotational state distribution, or the polarization of the rotational angular momentum, is most conveniently parametrized tluough multipole moments of the distribution [45]. Odd multipoles, such as the dipole, describe the orientation of the angidar momentum /, i.e. which way the tips of the / vectors preferentially point. Even multipoles, such as the quadnipole, describe the aligmnent of /, i.e. the spatial distribution of the / vectors, regarded as a collection of double-headed arrows. Orr-Ewing and Zare [47] have discussed in detail the measurement of orientation and aligmnent in products of chemical reactions and what can be learned about the reaction dynamics from these measurements. 

In most of the connnonly used ab initio quantum chemical methods [26], one fonns a set of configurations by placing N electrons into spin orbitals in a maimer that produces the spatial, spin and angular momentum syimnetry of the electronic state of interest. The correct wavefimction T is then written as a linear combination of tire mean-field configuration fimctions qj = example, to describe the... 

The quantum numbers tliat are appropriate to describe tire vibrational levels of a quasilinear complex such as Ar-HCl are tluis tire monomer vibrational quantum number v, an intennolecular stretching quantum number n and two quantum numbers j and K to describe tire hindered rotational motion. For more rigid complexes, it becomes appropriate to replace j and K witli nonnal-mode vibrational quantum numbers, tliough tliere is an awkw ard intennediate regime in which neitlier description is satisfactory see [3] for a discussion of tire transition between tire two cases. In addition, tliere is always a quantum number J for tire total angular momentum (excluding nuclear spin). The total parity (symmetry under space-fixed inversion of all coordinates) is also a conserved quantity tliat is spectroscopically important. 

J and Vrepresent the rotational angular momentum quantum number and tire velocity of tire CO2, respectively. The hot, excited CgFg donor can be produced via absorjDtion of a 248 nm excimer-laser pulse followed by rapid internal conversion of electronic energy to vibrational energy as described above. Note tliat tire result of this collision is to... 

Suppose that W(r,Q) describes the radial (r) and angular (0) motion of a diatomic molecule constrained to move on a planar surface. If an experiment were performed to measure the component of the rotational angular momentum of the diatomic molecule perpendicular to the surface (Lz= -ih d/dQ), only values equal to mh (m=0,1,-1,2,-2,3,-3,...) could be observed, because these are the eigenvalues of ... 

The functions are known as the angular wave functions or, because they describe the distribution of p over the surface of a sphere of radius r, spherical harmonics. The quantum number n = l,2,3,...,oo and is the same as in the Bohr theory, is the azimuthal quantum number associated with the discrete orbital angular momentum values, and is... 

When M is an atom the total change in angular momentum for the process M + /zv M+ + e must obey the electric dipole selection mle Af = 1 (see Equation 7.21), but the photoelectron can take away any amount of momentum. If, for example, the electron removed is from a d orbital ( = 2) of M it carries away one or three quanta of angular momentum depending on whether Af = — 1 or +1, respectively. The wave function of a free electron can be described, in general, as a mixture of x, p, d,f,... wave functions but, in this case, the ejected electron has just p and/ character. 

The nuclei of many isotopes possess an angular momentum, called spin, whose magnitude is described by the spin quantum number / (also called the nuclear spin). This quantity, which is characteristic of the nucleus, may have integral or halfvalues thus / = 0, 5, 1, f,. . . The isotopes C and 0 both have / = 0 hence, they have no magnetic properties. H, C, F, and P are important nuclei having / = 5, whereas and N have / = 1. 

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. 

The Stern-Gerlach experiment demonstrated that electrons have an intrinsic angular momentum in addition to their orbital angular momentum, and the unfortunate term electron spin was coined to describe this pure quantum-mechanical phenomenon. Many nuclei also possess an internal angular momentum, referred to as nuclear spin. As in classical mechanics, there is a relationship between the angular momentum and the magnetic moment. For electrons, we write... 

This term describes a shift in energy by Acim rn, for an orbital with quantum numbers I — 2, mi and that is proportional to the average orbital angular momentum (/z) for the TOj-spin subsystem and the so-called Racah parameters Bm, that in turn can be represented by the Coulomb integrals and The operator that corresponds to this energy shift is given by... 

---