Provided by: psi3_3.4.0-6ubuntu1_amd64 
NAME
cscf - solves the Hartree-Fock equations
DESCRIPTION
The program cscf carries out the iterative procedure to solve the Hartree-Fock equations.
This program is restricted to D2h symmetry and its subgroups and the orbital occupations
are required to be integers. Thus, certain pure angular momentum states derived from
partial occupation of degenerate orbitals cannot be obtained with the present codes. For
example, the 2PIu (doublet PI u) state of linear O-N-O derived from the lowest energy
linear (pi u)1 configuration may only be computed as the 2B2u (doublet B2u) or 2B3u
(doublet B 3u) component of the 2PIu (doublet PI u) state, and the resulting spatial
wavefunction will not have PI symmetry. In a certain sense, however, this is desirable,
as the energy will be a continuous function of the bending angle. Calculating the energy
of bent configurations as 2B2u (doublet B 2u) or 2B3u (doublet B 3u) and doing a pure 2PIu
(doublet PI u) state at linear geometries results in a pronounced discontinuity.
For the most part, triplet states resulting from double occupation of a doubly degenerate
orbital, such as the 3A2 (triplet A 2) state resulting from the (e')2 or (e")2
configurations in D3h symmetry, or the 3SIGMAg (triplet SIGMA g) state of a (pi g)2 or (pi
u)2 configuration in Dinfh (D infinity h) symmetry, will have the proper spatial symetry.
The singlet states resulting from these same electronic configurations are inherently
multiconfiguration and, as such, are not well represented by single configuration
wavefunctions.
REFERENCES
PK-file method:
1. R. C. Raffenetti, Chem. Phys. Lett. 20 (1973) 335.
Molecular symmetry and closed shell HF calculations:
1. M.Dupuis, and H.F.King, Int. J. Quant. Chem. 11 (1977) 613.
DIIS for closed shell:
1. P. Pulay, Chem. Phys. Lett. 73 (1980) 393.
2. P. Pulay, J. Comp. Chem. 3 (1982) 556.
Coupling coefficients (alpha and beta) for open shell:
1. C. C. J. Roothaan, Rev. Mod. Phys. 32 (1960) 179.
Damping:
1. D. R. Hartree, "The Calculation of Atomic Structures" (Wiley: New York) 1957.
2. M. C. Zerner and M. Hehenberger, Chem. Phys. Lett. 62 (1979) 550.
Level shifting:
1. V. R. Saunders and I. H. Hillier, Int. J. Quant. Chem. 7 (1973) 699.
CONVERGING CSCF
For difficult open shell cases, it is recommended that an appropriate closed shell
calculation be run first (add or remove an extra electron) and that this SCF vector then
be used as a guess for the desired open shell wavefunction. For TCSCF cases, it is always
wise to run a closed shell (or perhaps the appropriate triplet) SCF first and then use
this as a guess for the TCSCF.
For open shell systems, a level shift value of 0.5 to 3.0 is recommended. Start with a
high value (2.0 - 3.0) for the first SCF calculation and then reduce it (to 0.5 - 1.0) for
subsequent runs which use a converged SCF vector as the starting point.
It is extremely important to note that this version of the code no longer supports
OPENTYPE. One must use the new keywords REFERENCE and MULTP to specify the type of SCF
needed.
INPUT FORMAT
The cscf program searches through the default keyword path (first SCF and then DEFAULT)
for the following keywords:
LABEL = string
This is a character string to be included in the output. This string is not used
by the program. There is no default.
WFN = string
This is the type of wavefunction which is ultimately desired. The default is SCF.
OPENTYPE is no longer supported
REFERENCE = string
This specifies the type of SCF calculation one wants to do. It can be one of RHF
(for a closed shell singlet), ROHF (for a restricted open shell calculation), UHF
(for an unrestricted open shell calculation), TWOCON (for a two configuration
singlet), or SPECIAL. If SPECIAL is given, then alpha and beta coupling
coefficients must be given with the ALPHA and BETA keywords. The default is RHF.
MULTP= integer
Specifies the multiplicity of the molecule. Default is singlet.
CHARGE= integer
Specifies the charge of the molecule. Defauly is 0.
DOCC = integer_vector
This gives the number of doubly occupied orbitals in each irreducible
representation. There is no default. If this is not given, CSCF will attempt to
guess at the occupations using the core hamiltonian.
SOCC = integer_vector
This gives the number of singly occupied orbitals in each irreducible
representation. There is no default.
DERTYPE = string
This specifies the order of derivative that is to eventually be done. It is used
by the scf program to determine if certain files are to be written and it is also
used to determine the default convergence of the wavefunction. The default is
FIRST.
MAXITER = integer
This gives the maximum number of iterations. The default is 40.
CONVERGENCE = integer
This specifies how tightly the wavefunction will be converged. Convergence is
determined by comparing the RMS change in the density matrix ("delta P") to the
given value. The convergence criterion is 10**(-integer). The default is 7 if
both DERTYPE = NONE and WFN = SCF are given and 10 otherwise.
LEVELSHIFT = real
This specifies the level shift. The default is 1.
DIRECT = boolean
Specifies whether to do the SCF calculation with an integral direct technique. The
default is false.
PRINT_MOS = boolean
Specifies whether to print the molecular orbitals or not. The default is false.
There are also a large number of less commonly used input parameters. If you do not
understand what the following options mean, then make sure that they do not appear in your
input. The defaults will work in the overwhelming majority of cases. These are specified
with the following keywords:
DELETE_INTS = boolean
Integrals files will be erased if WFN = SCF and DERTYPE = FIRST or DERTYPE = NONE.
If you wish to keep integrals files then set DELETE_INTS = false. The default is
true.
REORDER = string
The parameter controls reordering of molecular orbitals. If set to BEFORE then the
guess orbitals from checkpoint file will be reordered. If set to AFTER, converged
orbitals will be reordered before being written to the checkpoint file. In either
case MOORDER parameter must be given to specify the reordering map. The default is
not to reorder orbitals.
MOORDER = integer_vector
This specifies a molecular orbital reordering vector. It will only be used if
REORDER is set. This vector maps every orbital to its new index, e.g. MOORDER = (0
2 1) specifies that after reordering orbitals 1 and 2 will be swapped. The rank of
this vector is the same as the number of MOs. The indices are in Pitzer order
(ordered by symmetry, then by energy within each symmetry block), base-0. CSCF
will likely fail if the given MOORDER mixes orbitals from different irreps. There
is no default.
ALPHA = real_vector
If OPENTYPE = SPECIAL, then this parameter gives the alpha coupling coefficients.
The number of elements in this vector is MM(MM+1)/2, where MM is the number of
irreducible representations containing singly occupied molecular orbitals. There
is no default.
BETA = real_vector
If OPENTYPE = SPECIAL, then this parameter gives the beta coupling coefficients.
The number of elements in this vector is MM(MM+1)/2, where MM is the number of
irreducible representations containing singly occupied molecular orbitals. There
is no default.
GUESS = string
This option determines the type of initial guess at the eigenvector CSCF will use.
The only valid option at the moment are : (1) GUESS = CORE, which causes it to use
core Hamiltonian eigenvector to start the calculation; (2) GUESS = AUTO which
results in an attempt to use the MO vector in the checkpoint file, or resorts to
core guess if there is no eigenvector in that file. The default if AUTO.
IPRINT = integer
This is a print option. The default is 0.
MO_OUT = boolean
Prints out the orbitals with symmetry and occupations at the end of the
calculation. Default is true.
ROTATE = boolean
The molecular orbitals will not be rotated if this is false. The rotation only
affects the virtual orbitals for open shell systems. This parameter must be true
for correlated gradients and it must be false for second and higher derivatives.
The default is false if WFN = SCF and true otherwise.
CHECK_ROT = boolean
Check the molecular orbital rotation described above to ensure that no columns of
the SCF eigenvector matrix are swapped by the rotation. Has no effect if ROTATE =
false. The default is true.
CHECK_MO_ORTHOGONALITY = boolean
Check if the molecular orbitals are orthonormal. Useful for debugging only. The
default is false.
DIIS = boolean
This determines whether diis will be used. The default is true.
DIISSTART = integer
This gives the first iteration for which DIIS will be used. The default is 0.
NDIIS = integer
This gives the number of error matrices to use in the diis procedure. The default
is 6 for closed shell, 4 for open shell, and 3 for tcscf.
DIISDAMP = real
This gives the damping factor for the diis procedure. The default is 0.0 for
closed shell, 0.02 for open shell, and 0.01 for tcscf.
INCR = real
This is used in tcscf to determine how often the ci coefficients are recalculated.
A small number (~0.25) will cause them to be recalculated nearly every scf
iteration. The default is 0.25.
DYN_ACC = boolean
When performing direct scf this specifies whether dynamic integral accuracy cutoffs
will be used. Default is true (use dynamic cutoffs). Initial iterations are
performed with integrals accurate to six digits. After density is converged to
10^-5 or 30 iterations are completed, full integral accuracy is used. If scf
convergence problems are experienced disabling dynamic cutoffs by setting this
variable to false might help.
ORTHOG_ONLY = boolean
Sometimes in CASSCF or other non-HF/KS schemes for orbital optimization, it is
useful to reorthogonalize MO's from other geometries for the current geometry so
they can be used as an initial guess for the new MO's. This can be performed by
running CSCF with ORTHOG_ONLY = true. After the orbitals are orthogonalized, the
program will quit without performing an SCF computation. This keyword will be
ignored if there are no previous orbitals in the checkpoint file. Defaults to true
if WFN = DETCAS.
30 May, 1991 cscf(1)