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Basis split-valence type

Each CGTO can be considered as an approximation to a single Slater-type orbital (STO) with effective nuclear charge f (zeta). The composition of the basis set can therefore be described in terms of the number of such effective zeta values (or STOs) for each electron. A double-zeta (DZ) basis includes twice as many effective STOs per electron as a single-zeta minimal basis (MB) set, a triple-zeta (TZ) basis three times as many, and so forth. A popular choice, of so-called split-valence type, is to describe core electrons with a minimal set and valence electrons with a more flexible DZ (or higher) set. [Pg.712]

Turning now to the intensities of the various modes, the data in Table 3.47 indicate that a polarized basis set like 6-31 G(d,p) offers a reasonable alternative to a much more extended set such as 6-31 + +G(2d,2p), even if not quantitatively very accurate. The split-valence 4-3 IG is considerably poorer, and the data with 3-21G are much worse, even though formally of split-valence type as well. The intensity magnification ratios induced upon dimerization... [Pg.173]

Since the first quantum mechanical calculation of phenol performed in 1967 using the CNDO/2 method" , the phenol geometry was considered at a variety of computational levels "" ranging from the HE to the MP2 method of molecular orbital theory and density functional theory (DFT) employed with several basis sets, mainly of the split valence type as, e.g. 6-31G(d,p) and 6-31- -G(d,p). These computational results are summarized in Tables 1-3 and Figure 4. It seems noteworthy that the semi-empirical geometries listed in Table 1 are rather close to the experimental observations. Also, to complete the theoretical picture of the phenol molecule, its theoretical inertia moments calculated at the B3LYP/6-31- -G(d,p) level are equal to 320.14639, 692.63671 and 1012.78307 a.u. [Pg.20]

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]

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]

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]

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]

The next step up in basis set size is a Triple Zeta (TZ). Such a basis contains three times as many functions as tire minimum basis, i.e. six s-functions and three p-functions for the first row elements. Some of the core orbitals may again be saved by only splitting the valence, producing a triple split valence basis set. Again the term TZ is used to cover both cases. The names Quadruple Zeta (QZ) and Quintuple Zeta (5Z, not QZ) for the next levels of basis sets are also used, but large sets are often given explicitly in terms of the number of basis functions of each type. [Pg.152]

For most molecules studied, modest Hartree-Fock calculations yield remarkably accurate barriers that allow confident prediction of the lowest energy conformer in the S0 and D0 states. The simplest level of theory that predicts barriers in good agreement with experiment is HF/6-31G for the closed-shell S0 state (Hartree-Fock theory) and UHF/6-31G for the open-shell D0 state (unrestricted Hartree-Fock theory). The 6-31G basis set has double-zeta quality, with split valence plus d-type polarization on heavy atoms. This is quite modest by current standards. Nevertheless, such calculations reproduce experimental barrier heights within 10%. [Pg.176]

IG and 6-3IG. These are commonly used split-valence plus polarization basis sets. These basis sets contain inner-shell functions, written as a linear combination of six Gaussians, and two valence shells, represented by three and one Gaussian primitives, respectively (noted as 6-3IG). When a set of six d-type Gaussian primitives is added to each heavy atom and a single set of Gaussian p-type functions to each hydrogen atom, this is noted as and... [Pg.38]

Basis sets for use in practical Hartree-Fock, density functional, Moller-Plesset and configuration interaction calculations make use of Gaussian-type functions. Gaussian functions are closely related to exponential functions, which are of the form of exact solutions to the one-electron hydrogen atom, and comprise a polynomial in the Cartesian coordinates (x, y, z) followed by an exponential in r. Several series of Gaussian basis sets now have received widespread use and are thoroughly documented. A summary of all electron basis sets available in Spartan is provided in Table 3-1. Except for STO-3G and 3 -21G, any of these basis sets can be supplemented with additional polarization functions and/or with diffuse functions. It should be noted that minimal (STO-3G) and split-valence (3-2IG) basis sets, which lack polarization functions, are unsuitable for use with correlated models, in particular density functional, configuration interaction and Moller-Plesset models. Discussion is provided in Section II. [Pg.40]

A split-valence basis set represents core atomic orbitals by one set of functions and valence atomic orbitals by two sets of functions. Hydrogen is provided by two s-type functions, and main-group elements are provided two sets of valence s and p-type functions. [Pg.43]

The second shortcoming of a minimal (or split-valence) basis set... functions being centered only on atoms. . . may be addressed by providing d-type functions on main-group elements (where the valence orbitals are of s and p type), and (optionally) p-type functions on hydrogen (where the valence orbital is of s type). This allows displacement of electron distributions away from the nuclear positions. [Pg.43]

G The 3-21G Basis Set supplemented by d-type Gaussians for each second-row and heavier main-group elements only. 3-2IG is a supplemented Split-Valence Basis Set. [Pg.753]

The valence AOs in a molecule might be expected to vary much more with their environment than the inner core) AOs. Thus, an economical way to construct a basis set is to use a single basis function to represent the core AOs, but to use two independent basis functions to represent the valence AOs. This type of basis set is called a split-valence basis set. [Pg.971]


See other pages where Basis split-valence type is mentioned: [Pg.159]    [Pg.160]    [Pg.116]    [Pg.100]    [Pg.315]    [Pg.55]    [Pg.87]    [Pg.88]    [Pg.159]    [Pg.160]    [Pg.471]    [Pg.203]    [Pg.204]    [Pg.88]    [Pg.309]    [Pg.258]    [Pg.261]    [Pg.90]    [Pg.258]    [Pg.261]    [Pg.262]    [Pg.160]    [Pg.147]    [Pg.6]    [Pg.138]    [Pg.139]    [Pg.171]    [Pg.38]    [Pg.194]    [Pg.523]    [Pg.3]    [Pg.25]   
See also in sourсe #XX -- [ Pg.100 ]

See also in sourсe #XX -- [ Pg.100 ]




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Split valence

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