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Valence split

The solution to this problem is to use more than one basis function of each type some of them compact and others diffuse, Linear combinations of basis Functions of the same type can then produce MOs with spatial extents between the limits set by the most compact and the most diffuse basis functions. Such basis sets arc known as double is the usual symbol for the exponent of the basis function, which determines its spatial extent) if all orbitals arc split into two components, or split ualence if only the valence orbitals arc split. A typical early split valence basis set was known as 6-31G 124], This nomenclature means that the core (non-valence) orbitals are represented by six Gaussian functions and the valence AOs by two sets of three (compact) and one (more diffuse) Gaussian functions. [Pg.385]

Split valence basis sets generally give much better results than minimal ones, but at a cost. Remember that the number of two-electron integrals is proportional to kf , where W is the number of basis functions. Whereas STO-3G has only live ba.sis functions for carbon, 6-31G has nine, resulting in more than a tenfold increase in the size of the calculation,... [Pg.385]

Although split valence basis sets give far better results than minimal ones, they still have systematic weaknesses, such as a poor description of three-inembered rings, This results from their inability to polarize the electron density to one side of an atom. Consider the /T-bond shown in Figure 7-23. [Pg.385]

Th e con traction expon en ts and cocfTicien ts of th e d-type functions were optinii/ed using five d-primitives (the first set of d-type functions) for the STO-XG basis sets and six d-primitives (the second set of d-type functions ) for the split-valence basis sets. Thus, five d orbitals are recommended for the STO-XG basis sets and six d orhitals for the split-valence basis sets. [Pg.116]

Split-Valence Basis Sets. In split-valence basis sets, inner or core atomic orbitals ar e represented by one basis function and valence atomic orbitals are represented by two. The carbon atom in methane is represented by one Is inner orbital and 2(2s, 2pj., 2py, 2pj) = 8 valence orbitals. Each hydrogen atom is represented by 2 valence orbitals hence, the number of orbitals is... [Pg.310]

A second issue is the practice of using the same set of exponents for several sets of functions, such as the 2s and 2p. These are also referred to as general contraction or more often split valence basis sets and are still in widespread use. The acronyms denoting these basis sets sometimes include the letters SP to indicate the use of the same exponents for s andp orbitals. The disadvantage of this is that the basis set may suffer in the accuracy of its description of the wave function needed for high-accuracy calculations. The advantage of this scheme is that integral evaluation can be completed more quickly. This is partly responsible for the popularity of the Pople basis sets described below. [Pg.79]

CREN Available for SC(4.v) through Hs(0.v6/)6d), this is a shape-consistent basis set developed by Ermler and coworkers that has a large core region and small valence. This is also called the CEP—4G basis set. The CEP—31G and CEP—121G sets are related split valence sets. [Pg.84]

Binkley, J.S. Pople, J.A. Hehre, W.J. Self-consistent molecular orbital methods. 21. Small split-valence basis sets for first-row elements J. Am. Chem. Soc. 102 939-947, 1980. [Pg.110]

Split Valence Basis Sets Polarized Basis Sets Diffuse Functions Pseudopotentials... [Pg.97]

The first way that a basis set can be made larger is to increase the number of basis functions per atom. Split valence basis sets, such as 3-21G and 6-31G, have two (or more) sizes of basis function for each valence orbital. For example, hydrogen and carbon are represented as ... [Pg.98]

The double zeta basis sets, such as the Dunning-Huzinaga basis set (D95), form all molecular orbitals from linear combinations of two sizes of functions for each atomic orbital. Similarly, triple split valence basis sets, like 6-3IIG, use three sizes of contracted functions for each orbital-type. [Pg.98]

Split valence basis sets allow orbitals to change size, but not to change shape. Polarized basis sets remove this limitation by adding orbitals with angular momentum beyond what is required for the ground state to the description of each atom. For example, polarized basis sets add d functions to carbon atoms and f functions to transition metals, and some of them add p functions to hydrogen atoms. [Pg.98]

G [H-Xe] Split valence 2 sets of functions in the valence region provide a more accurate representation of orbitals. Use for very large molecules for which 6-31G(d) is too expensive. 9 2 6D... [Pg.102]

We can further conclude that the success of the Cl-Singles method often depends critically on the chosen basis set. Diffuse (Rydberg-like) excited states usually require the addition of one or two diffuse functions to a split-valence basis set. [Pg.224]

Basis Set Type Minimal Split-valence Polarized Diffuse High ang. momentum... [Pg.266]

The chemical bonding occurs between valence orbitals. Doubling the 1 s-functions in for example carbon allows for a better description of the 1 s-electrons. However, the Is-orbital is essentially independent of the chemical environment, being very close to the atomic case. A variation of the DZ type basis only doubles the number of valence orbitals, producing a split valence basis. In actual calculations a doubling of tire core orbitals would rarely be considered, and the term DZ basis is also used for split valence basis sets (or sometimes VDZ, for valence double zeta). [Pg.152]


See other pages where Valence split is mentioned: [Pg.110]    [Pg.257]    [Pg.257]    [Pg.258]    [Pg.261]    [Pg.90]    [Pg.90]    [Pg.116]    [Pg.257]    [Pg.257]    [Pg.258]    [Pg.258]    [Pg.259]    [Pg.261]    [Pg.262]    [Pg.94]    [Pg.297]    [Pg.301]   
See also in sourсe #XX -- [ Pg.385 ]

See also in sourсe #XX -- [ Pg.184 ]




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Basis split-valence type

Double zeta and split valence basis sets

INDEX split valence

MIDI split valence contracted basis

Single-, Multiple-, and Split-Valence

Split valence basis sets

Split valence double zeta basis sets

Split valence polarization

Split valence zeta

Split valence-shell basis set

Split-valence basis

Split-valence basis sets orbital energy calculations using

Split-valence gaussian basis sets

Split-valence plus polarization

Split-valence plus polarization basis

Valence band spin-orbit splitting

Valence band splitting

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