The Integral keyword modifies the method of computation and use of two-electron integrals and their derivatives.
Integration Grid Selection Option
Specifies the integration grid to be used for numerical integrations. Note that it is very important to use the same grid for all calculations where you intend to compare energies e.g., computing energy differences, heats of formation, and so on.
“Pruned” grids are grids that have been optimized to use the minimal number of points required to achieve a given level of accuracy. Pruned grids are used by default when available, currently defined for H through Kr. For example FineGrid is a pruned (75,302 grid), having 75 radial shells and 302 angular points per shell, resulting in about 7000 points per atom. UltraFine requests a pruned (99,590) grid. It is recommended for molecules containing lots of tetrahedral centers and for computing very low frequency modes of systems. This grid is also useful for optimizations of larger molecules with many soft modes such as methyl rotations, making such optimizations more reliable. SuperFineGrid is a more accurate grid than UltraFine; SuperFineGrid is a pruned 175,974 for first-row atoms and 250,974 for atoms in the second and later rows.
Other special values for this parameter are CoarseGrid, which requests a pruned version of the (35,110) grid, and SG1Grid, a pruned version of (50,194). Note, however, that the FineGrid has considerably better numerical accuracy and rotational invariance than these other grids, and they are not recommended for production calculations [Krack98]. Pass0Grid requests the obsolete pruned (35,110) grid once intended for pass 0 of a tight SCF calculation.
The default grid is FineGrid. In this case, the default grid for the CPHF is Coarse. When UltraFine is used for the integrals, then SG1 is used for the CPHF; if SG1 is selected as the integration grid, the Coarse grid is again used for the CPHF. When a specific grid is specified to the Int=Grid option, then that grid is also used for the CPHF. Finally, be aware that SG1 is used in the CPHF as the default integration grid for a few DFT jobs including Polar=OptRot, Freq=Anharmonic, and Freq=NNROA.
The parameter to this option is either a grid name keyword or a specific grid specification. If a keyword is chosen, then the option name itself may be omitted (i.e., Integral(Grid=UltraFineGrid) and Integral(UltraFineGrid) are equivalent).
Specific grids may be selected by giving an integer value N as the argument to Grid. N may have one of these forms:
- A large positive integer of the form mmmnnn, which requests a grid with mmm radial shells around each atom, and nnn angular points in each shell. The total number of integration points per atom is thus mmm*nnn. For example, to specify the (99,302) grid, use Int(Grid=99302). The valid numbers of angular points are 38, 50 [Lebedev75], 72 [McLaren63], 86, 110 [Lebedev75], 146, 194, 302 [Lebedev76], 434 [Lebedev80], 590, 770, and 974 [Lebedev92]. If a larger number of angular points is desired, a spherical product grid can be used.
- A large negative integer of the form –mmmnnn, which requests mmm radial shells around each atom, and a spherical product grid having nnn θ points and 2*nnn φ points in each shell. The total number of integration points per atom is therefore 2*mmm*nnn2. This form is used to specify the (96,32,64) grid commonly cited in benchmark calculations: Int(Grid=-96032).
Note that any value for nnn is permitted; although, small values are silly (values of nnn < 15 produce grids of similar size and inferior performance to the special angular grids requested by the second format above). Large values are expensive. For example, a value of 200100 would use 2*200*100*100 or 4 million points per atom!
Requests a Douglas-Kroll-Hess 2nd order scalar relativistic calculation [Douglas74, Hess85, Hess86, Jansen89] (see [Barysz01, deJong01] for an overview). This method uses a Gaussian nuclear model [Visscher97]. DKH2 and DouglasKrollHess are synonyms.
Algorithm Selection Options
Set the threshold size for turning on FMM by default to N. The default is 60 atoms. Molecules with symmetry have higher crossover points, and the threshold is increased accordingly, to 120 atoms for the C2 and Cs point groups and 240 atoms for higher symmetry.
NoSymm disables and Symm enables the use of symmetry in the evaluation and storage of integrals (Symm is the default). Synonymous with the keywords Symm=[No]Int, which is the recommended usage.
Trace Linda transactions. Primarily for debugging.
Set ECP accuracy parameter to N.
Set 2-electron integral accuracy to 10–N. The default is 10-12.
Transform integrals from Cartesian to Pure form before digesting them (contracting with density matrices during direct calculations). The default is to decide the based on parameters such as how many density matrices are being processed.
Skip tests of numerical accuracy of XC quadrature.
Read common /B/ from disk after the initial geometry, even if a standard basis was set up.
General Basis Set-Related Options
Whether to write out regular or the Raffenetti integrals. Raff and Raff1 integrals write the Raffenetti1 integrals. Raff2 and Raff3 will write the 1 and 2/1,2 and 3 Raffenetti integral combinations (respectively). Primarily useful with External or Output=MatrixElement. NoRaff suppresses writing the Raffenetti integrals and writes out the regular integrals.
Transform generalized contraction basis sets to reduce the number of primitives, neglecting primitives with coefficients of 10-N or less. This is the default, with N=4.
Transform generalized contraction basis sets to reduce the number of primitives, but using only transformations which are exact. Only exact duplicate primitives are removed, and there will be no change in the energy value.
Do not transform generalized contraction basis sets to reduce the number of primitives.
Last updated on: 07 October 2016. [G16 Rev. A.03]