Matrix elements symmetry

Aspects of the Jahn-Teller symmetry argument will be relevant in later sections. Suppose that the electronic states aie n-fold degenerate, with symmetry at some symmetiical nuclear configuration Qq. The fundamental question concerns the symmetry of the nuclear coordinates that can split the degeneracy linearly in Q — Qo, in other words those that appeal linearly in Taylor series for the matrix elements A H B). Since the bras (/1 and kets B) both transform as and H are totally symmetric, it would appear at first sight that the Jahn-Teller active modes must have symmetry Fg = F x F. There... 

The symmetry argument actually goes beyond the above deterniination of the symmetries of Jahn-Teller active modes, the coefficients of the matrix element expansions in different coordinates are also symmetry determined. Consider, for simplicity, an electronic state of symmetiy in an even-electron molecule with a single threefold axis of symmetry, and choose a representation in which two complex electronic components, e ) = 1/v ( ca) i cb)), and two degenerate complex nuclear coordinate combinations Q = re " each have character T under the C3 operation, where x — The bras e have character x. Since the Hamiltonian operator is totally symmetric, the diagonal matrix elements e H e ) are totally symmetric, while the characters of the off-diagonal elements ezf H e ) are x. Since x = 1, it follows that an expansion of the complex Hamiltonian matrix to quadratic terms in Q. takes the form... 

Symmetry considerations forbid any nonzero off-diagonal matrix elements in Eq. (68) when f(x) is even in x, but they can be nonzero if f x) is odd, for example,/(x) = x. (Note that x itself hansforms as B2 [284].) Figure 3 shows the outcome for the phase by the continuous phase tracing method for cycling... 

A final point to be made concerns the symmetry of the molecular system. The branching space vectors in Eqs. (75) and (76) can be obtained by evaluating the derivatives of matrix elements in the adiabatic basis... 

The eigenvalues of this mabix have the form of Eq. (68), but this time the matrix elements are given by Eqs. (84) and (85). The symmetry arguments used to determine which nuclear modes couple the states, Eq. (81), now play a cracial role in the model. Thus the linear expansion coefficients are only nonzero if the products of symmebies of the electronic states at Qq and the relevant nuclear mode contain the totally symmebic inep. As a result, on-diagonal matrix elements are only nonzero for totally symmebic nuclear coordinates and, if the elecbonic states have different symmeby, the off-diagonal elements will only... 

The remaining combinations vanish for symmetry reasons [the operator transforms according to B (A") hreducible representation]. The nonvanishing of the off-diagonal matrix element fl+ is responsible for the coupling of the adiabatic electronic states. 

In these eases, one says that a linear variational ealeulation is being performed. The set of funetions Oj are usually eonstrueted to obey all of the boundary eonditions that the exaet state E obeys, to be funetions of the the same eoordinates as E, and to be of the same spatial and spin symmetry as E. Beyond these eonditions, the Oj are nothing more than members of a set of funetions that are eonvenient to deal with (e.g., eonvenient to evaluate Hamiltonian matrix elements I>i H j>) and that ean, in prineiple, be made eomplete if more and more sueh funetions are ineluded. 

Symmetry provides additional quantum numbers or labels to use in describing the mos. Each such quantum number further sub-divides the collection of all mos into sets that have vanishing Hamiltonian matrix elements among members belonging to different sets. 

One Must be Able to Evaluate the Matrix Elements Among Properly Symmetry Adapted N-Electron Configuration Eunctions for Any Operator, the Electronic Hamiltonian in Particular. The Slater-Condon Rules Provide this Capability... 

Molecular point-group symmetry can often be used to determine whether a particular transition s dipole matrix element will vanish and, as a result, the electronic transition will be "forbidden" and thus predicted to have zero intensity. If the direct product of the symmetries of the initial and final electronic states /ei and /ef do not match the symmetry of the electric dipole operator (which has the symmetry of its x, y, and z components these symmetries can be read off the right most column of the character tables given in Appendix E), the matrix element will vanish. 

The second term in the above expansion of the transition dipole matrix element Za 3 if i/3Ra (Ra - Ra,e) can become important to analyze when the first term ifi(Re) vanishes (e.g., for reasons of symmetry). This dipole derivative term, when substituted into the integral over vibrational coordinates gives... 

It is through sueh symmetry and eoupling matrix element eonsiderations that one ean often guess whether a given perturbation will have an appreeiable effeet on the state of interest. 

In order to adapt that expression to the problem at hand, we note that interaction matrix elements for shaking and breathing modes are different. Namely, the matrix element AfiV, symmetry index (A or E), is very small for even I + I, while the cosine matrix element, M - = is minor for odd I + I [Wurger 1989]. At low temperatures, when only / = / is accessible, the shaking... 

If the system contains symmetry, there are additional Cl matrix elements which become zero. The symmetry of a determinant is given as the direct product of the symmetries of the MOs. The Hamilton operator always belongs to the totally symmetric representation, thus if two determinants belong to different irreducible representations, the Cl matrix element is zero. This is again fairly obvious if the interest is in a state of a specific symmetry, only those determinants which have the correct symmetry can contribute. 

Employing a C2 symmetry in the case of the thiirene 1-dioxide and remembering that the spiro-operator that mixes the fragment orbitals gives nonzero matrix elements only if these orbitals are symmetric to the C2 operation53, the net result is stabilizing. On the other hand, thiirene 1-oxide suffers a homoconjugative destabilization. 

A computer program for the theoretical determination of electric polarizabilities and hyperpolarizabilitieshas been implemented at the ab initio level using a computational scheme based on CHF perturbation theory [7-11]. Zero-order SCF, and first-and second-order CHF equations are solved to obtain the corresponding perturbed wavefunctions and density matrices, exploiting the entire molecular symmetry to reduce the number of matrix element which are to be stored in, and processed by, computer. Then a /j, and iap-iS tensors are evaluated. This method has been applied to evaluate the second hyperpolarizability of benzene using extended basis sets of Gaussian functions, see Sec. VI. 

Owing to permutational symmetry, at most six second-order matrices are independent. To accoimt for point molecnlar symmetry let ns introdnce the symmetrized Kronecker square of T, with matrix elements [4]... 

The evaluation of the radial coupling matrix elements between molecular states of the same symmetry 3... 

It was shown above that the cubic term in the potential function for the anharmonic oscillator cannot, for reasons of symmetry, contribute to a first-order perturbation. However, if the matrix elements of = ax3 are evaluated, it is found that this term results in a second-order correction to the... 

With its substitution in Eq. (99) it becomes evident from the orthogonality of the Hermite polynomials, that all matrix elements are equal to zero, with the exception of v = v — 1 and vf = u +1. Thus, the selection rule for vibrational transitions (in the harmonic approximation) is An — 1. It is not necessary to evaluate the matrix elements unless there is an interest in calculating the intensities of spectral features resulting from vibrational transitions (see problem 18). It should be evident that transitions such as Av - 3 are forbidden under this more restrictive selection rule, although they are permitted under the symmetry selection rule developed in the previous paragraphs. 

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