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Lowest energy state

To illustrate the use of the variational prineiple, results are presented here for ealeulations of the five lowest energy states (the ground state and the first four exeited states) of a partiele subjeet to the potential... [Pg.41]

The orthogonality condition assures one that the lowest energy state will not converge to core-like states, but valence states. The wavefimction for the solid can be written as... [Pg.113]

Methods that are based on making the fiinctional (T // T ) / ( T T ) stationary yield upper bounds to the lowest energy state having the synnnetry of the CSFs in T. The Cl and MCSCF methods are of this type. [Pg.2186]

QMC teclmiques provide highly accurate calculations of many-electron systems. In variational QMC (VMC) [112, 113 and 114], the total energy of the many-electron system is calculated as the expectation value of the Hamiltonian. Parameters in a trial wavefiinction are optimized so as to find the lowest-energy state (modem... [Pg.2220]

Request either the lowest energy state of the specified m ii Iti-plieity or the n exi lowest energy stale for sem i-em pirical calculation s. [Pg.234]

VV e now wish to establish the general functional form of possible wavefunctions for the two electrons in this pseudo helium atom. We will do so by considering first the spatial part of the u a efunction. We will show how to derive functional forms for the wavefunction in which the i change of electrons is independent of the electron labels and does not affect the electron density. The simplest approach is to assume that each wavefunction for the helium atom is the product of the individual one-electron solutions. As we have just seen, this implies that the total energy is equal to the sum of the one-electron orbital energies, which is not correct as ii ignores electron-electron repulsion. Nevertheless, it is a useful illustrative model. The wavefunction of the lowest energy state then has each of the two electrons in a Is orbital ... [Pg.57]

Interactions between nonpolar compounds are generally stronger in water than in organic solvents. At concentrations where no aggregation or phase separation takes place, pairwise hydrophobic interactions can occur. Under these conditions, the lowest energy state for a solute molecule is the one in which it is completely surrounded by water molecules. However, occasionally, it will also meet other solute molecules, and form short-lived encounter complexes. In water, the lifetime of these complexes exceeds that in organic solvents, since the partial desolvation that accompanies the formation of these complexes is less unfavourable in water than in organic solvents. [Pg.167]

Ah initio programs attempt to compute the lowest-energy state of a specified multiplicity. Thus, calculations for different spin states will give the lowest-energy state and a few of the excited states. This is most often done to determine singlet-triplet gaps in organic molecules. [Pg.216]

The essential features of an NMR spectrometer shown m Figure 13 5 are not hard to understand They consist of a magnet to align the nuclear spins a radiofrequency (rf) transmitter as a source of energy to excite a nucleus from its lowest energy state to the next higher one a receiver to detect the absorption of rf radiation and a recorder to print out the spectrum... [Pg.523]

HyperChem semi-empirical methods usually let you request a calculation on the lowest energy state of a given multiplicity or the next lowest state of a given spin multiplicity. Since most molecules with an even number of electrons are closed-shell singlets without... [Pg.232]

This factor can be obtained from the vibration partition function which was omitted from the expression for the equilibrium constant stated above and is, for one degree of vibrational freedom where vq is the vibrational frequency in the lowest energy state. [Pg.49]

The remarkable thing is that the HF model is so reliable for the calculation of very many molecular properties, as 1 will discuss in Chapters 16 and 17. But for many simple applications, a more advanced treatment of electron correlation is essential and in any case there are very many examples of spectroscopic states that caimot be represented as a single Slater determinant (and so cannot be treated using the standard HF model). In addition, the HF model can only treat the lowest-energy state of any given symmetry. [Pg.187]

The solutions for the unperturbed Hamilton operator from a complete set (since Ho is hermitian) which can be chosen to be orthonormal, and A is a (variable) parameter determining the strength of the perturbation. At present we will only consider cases where the perturbation is time-independent, and the reference wave function is non-degenerate. To keep the notation simple, we will furthermore only consider the lowest energy state. The perturbed Schrodinger equation is... [Pg.123]

When pyrrole is irradiated, only decomposition products were obtained. Theoretical data can fit this statement (Fig. 6). In fact, the direct irradiation populates the excited singlet state, which can be converted into the Dewar pyrrole or into the corresponding triplet state. Clearly, the intersystem crossing to the triplet state allows the system to reach the lowest energy state. The excited triplet state can give the biradical intermediate, and this intermediate can give either the decomposition... [Pg.54]

As with the first and second laws, the Third Law is based on experimental measurements, not deduction. It is easy, however, to rationalize such a law. In a perfectly ordered3 crystal, every atom is in its proper place in the crystal lattice. At T— 0 Kelvin, all molecules are in their lowest energy state. Such a configuration would have perfect order and since entropy is a measure of the disorder in a system, perfect order would result in an entropy of zero.b Thus, the Third Law gives us an absolute reference point and enables us to assign values to S and not just to AS as we have been restricted to do with U, H, A, and G. [Pg.155]

Kelvin and hence, in their lowest energy states. At a temperature T, the collection of N molecules has an energy given by... [Pg.529]

You can think of the energy in a lycopene molecule as a wave sloshing in a bathtub, or the wave you can make with a jump rope. The lowest energy state, called the ground state, would correspond to the jump rope going around in the normal fashion. [Pg.108]


See other pages where Lowest energy state is mentioned: [Pg.275]    [Pg.276]    [Pg.390]    [Pg.429]    [Pg.2355]    [Pg.5]    [Pg.61]    [Pg.499]    [Pg.33]    [Pg.150]    [Pg.266]    [Pg.173]    [Pg.218]    [Pg.59]    [Pg.361]    [Pg.8]    [Pg.2269]    [Pg.16]    [Pg.141]    [Pg.59]    [Pg.190]    [Pg.147]    [Pg.147]    [Pg.703]    [Pg.205]    [Pg.137]    [Pg.260]    [Pg.486]    [Pg.146]    [Pg.802]    [Pg.29]    [Pg.329]   
See also in sourсe #XX -- [ Pg.64 ]

See also in sourсe #XX -- [ Pg.375 ]




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Lowest energy

Lowest energy excited state

Lowest energy excited state substitutions

Lowest energy transition state

Lowest state

Lowest-energy transition states, enamine

The Lowest Energy Excited Singlet State

Transition state of lowest energy

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