Q-Chem also supports ALMO-EDA calculations with one or multiple
fragments in non-aufbau electronic configurations.
This method is
particularly useful for cases where the energetically most stable electronic
state of a given fragment changes upon the formation of intermolecular
complex, which is common for systems involving open-shell species such
as carbenes, transition metal cations, etc. For example, the lowest-energy
electronic configuration of an isolated Ba radical cation is 6s;
however, when it is ligated with CO, the complex is more stable when
the unpaired electron of Ba is promoted from 6s to 5d, which
is thus in a non-aufbau state relative to the isolated Ba cation. A
sensible strategy to study the formation of such a complex is to perform
an ALMO-EDA calculation with Ba in the 5d electronic configuration,
and then evaluate the energy difference between Ba(5d) and
Ba(6s) and interpret that as the monomer “electronic preparation”
energy. To ensure that the system stays in a given non-aufbau electronic
configuration throughout, the Maximum Overlap Method
J. Phys. Chem. A
(2008), 112, pp. 13164. (MOM, see Sec. 4.5.11 for details) is applied to almost all stages in ALMO-EDA, including (i) isolated fragment calculations, (ii) calculation for the polarized wavefunction, and (iii) full SCF calculation for the whole system. Among them, (i) and (iii) are standard SCF calculations using MOM, while (ii) involves the application of MOM to an SCFMI calculation, 720 J. Chem. Phys.
(2020), 153, pp. 244111. which is compatible with the use of DIIS algorithm to solve locally projected SCF equations (with FRGM_METHOD = STOLL or GIA, see Section 12.4).
Specifically, an ALMO-EDA calculation for a complex within a non-aufbau electronic configuration (assuming only one of the fragments is excited) comprises the following steps:
Perform ground-state SCF calculations for all fragments
Calculate the non-aufbau electronic configuration for the fragment as specified in the input using MOM; construct the frozen state for the system with that one fragment in the non-aufbau state and the rest in ground state
Starting from the frozen state, perform an SCFMI calculation with MOM to obtain the polarized state within the non-aufbau electronic configuration
Perform a full SCF calculation with MOM, starting from the polarized wavefunction in the non-aufbau state
Such a calculation requires EDA2_MOM = TRUE in addition to the setup of standard EDA2 jobs. The non-aufbau electronic state is specified through the $scfmi_mom input section, which has the following format:
$scfmi_mom frag_idx1 X_1 Y_1 spin_1 frag_idx2 X_2 Y_2 spin_2 ... $end
In each row, the first entry specifies the index of the non-aufbau fragment (starting from 1). The second and third entries specify the non-aufbau electronic configuration, which is prepared by promoting an electron from a given fragment’s HOMOX to LUMOY once the ground-state SCF calculation of that fragment is finished. The last entry specifies the spin of the occupied and virtual orbitals that are being swapped (“a” for electrons and “b” for electrons, and orbitals will be used by default if the fourth entry is left blank). For instance, for a HOMOLUMO excitation on the first fragment, this section would simply look like
¯$scfmi_mom ¯1 0 0 a ¯$end ¯
Q-Chem 5 also allows one to perform SCFMI calculations for non-aufbau electronic
J. Chem. Phys.
(2020), 153, pp. 244111. without going through the entire ALMO-EDA procedure. To do that, one can simply add SCFMI_MOM = TRUE to the $rem setup of an SCFMI calculation (see Section 12.7.1). The non-aufbau electronic configuration can be specified through the $scfmi_mom section in the same way.
$molecule 1 2 -- 1 2 Ba 0.0 0.0 0.0 -- 0 1 C 0.0 0.0 2.734 O 0.0 0.0 3.876 $end $rem JOBTYPE EDA !by default EDA2 = 2 with CT analysis METHOD B3LYP BASIS DEF2-TZVP ECP DEF2-ECP UNRESTRICTED TRUE SCF_CONVERGENCE 8 SCF_ALGORITHM DIIS EDA2_MOM TRUE $end $scfmi_mom 1 0 2 $end