# 4.2.42. QMSTAT¶

## 4.2.42.1. Description¶

QMSTAT couples a quantum chemical region to a statistically mechanically described surrounding thus creating an effective Hamiltonian for the quantum chemical region \(H_{\text{eff.}}\). This way solvent effects can be accounted for.

The surrounding is discrete in contrast to the continuum models, such as PCM (also available in Molcas, see SEWARD). The explicit representation of the solvent enables a more accurate description of the solvation, but also makes the model more complex and significantly less “black-box”. For example, the interaction within the statistical mechanical surrounding has to be accounted for with an accurate enough force-field. In its present implementation QMSTAT only treats water as described by an early version of NEMO, which includes polarization of the molecules [99]. Also, the interaction between the quantum chemical region (typically the solute) and the surrounding (typically the solvent) has to be considered in more detail than in a continuum model. Several approaches to discrete (or explicit) solvation are thus possible. The approach in QMSTAT is summarized below, see also [100][101][102][103].

To include entropic effects to the solvation phenomena,
QMSTAT uses the Metropolis–Monte Carlo simulation
technique. This means that random steps are taken in the
space of solute–solvent configurations, some of which are
accepted, others rejected, on account of the usual energy
difference criteria. This implies that at each step, an
energy has to be evaluated. Using normal quantum chemical
methods, this is usually too restrictive, since roughly one
million Monte Carlo steps are required to converge the statistical
mechanical treatment. QMSTAT proceeds by doing
simplifications to the quantum chemistry, not the statistical
mechanics, as is the more common way forward. QMSTAT
is therefore a *hybrid* QM/MM methods (according to one
existing terminology).

Two simplified quantum chemical methods are presently available: orbital basis Hartree–Fock and a state basis formulation, which is approximate to the CASSCF method. Both formulations uses the fact that there is only minor differences in the electronic structure for the different configurations in the Monte Carlo simulation. Therefore, a basis as general as the standard atomic orbital basis sets is redundant. QMSTAT constructs either a more compact orbital basis or a more compact basis in terms of states to expand the solvated wave function. This requires some work before the simulation, but has the advantage that during the simulation, less computational work is needed.

Finally, a comment on the way the energy is computed for a given configuration is needed. The evaluation of the interactions between the solvent molecules is prescribed by the construction of the force-field and are relatively simple. The interaction between the quantum chemical region and the solvent is formulated to include electrostatic and non-electrostatic interactions. The former is described in a multi-center multipole expanded way, while the latter models the effect the antisymmetry principle between solute and solvent electrons has on the solute electronic structure. Its formulation is similar to pseudo-potentials. Also a phenomenological term for the dispersion is added. Long range electrostatics, finally, is described with a dielectric cavity model.

## 4.2.42.2. Dependencies¶

The dependencies of QMSTAT differ for the two quantum chemical methods. In the Hartree–Fock description, SEWARD, FFPT, SCF, AVERD, MPPROP and MOTRA typically have to precede. If an orbital basis is taken from somewhere else FFPT, SCF and AVERD are not mandatory. For the RASSI alternative, typically SEWARD, SCF, RASSCF, MPPROP and RASSI precede QMSTAT.

## 4.2.42.3. Files¶

Below is a list of the files that are used/created by the program QMSTAT.

### 4.2.42.3.1. Input files¶

- ONEINT
- One-electron integral file generated by the program SEWARD.
- RUNFILE
- File for communication of auxiliary information generated by the program SEWARD.
- RUNFILEW
- File for communication of auxiliary information generated by the program SEWARD for the solvent molecule.
- AVEORB
- (Only for Hartree–Fock alternative). Average orbitals generated by AVERD. If other orbitals are to be used, they should be given the above name; in other words, the orbitals must not be created by AVERD, it is only customary.
- SOLORB
- Solvent orbitals generated by SCF.
- TRAONE
- (Only for Hartree–Fock alternative). Molecular orbital transformed one-electron integrals generated by MOTRA.
- TRAINT
- (Only for Hartree–Fock alternative). Molecular orbital transformed two-electron integral generated by MOTRA.
- MPPROP
- File generated by MPPROP.
- DIFFPR
- Exponents and Prefactors for a Slater desciption of the Electrostatics to take into account the penetration effects due to the overlap. File generated by MPPROP.
- RASSIM
- (Only for the RASSI alternative). The transition density matrix generated by RASSI. The keyword TOFILE has to be given in the input to RASSI.
- EIGV
- (Only for the RASSI alternative). Information about the eigenvectors and their energy generated by RASSI (TOFILE needed).
- ADDON*
- File with additional one-electron perturbation to be added to the Hamiltonian matrix. This file is only required if EXTERNAL is used.

### 4.2.42.3.2. Output files¶

- STFIL*
- Start files in which solvent configurations are stored at intervals during the simulation. They enable the simulation to restart, hence they can also be as input to QMSTAT.
- SAFIL*
- Sampling files in which a selection of configurations are stored for analysis. They can in some applications also act as input to QMSTAT, usually in free-energy perturbation calculations.
- EXTRA*
- Extract files which are formatted files in which data from the analysis of the sampling files are stored.

## 4.2.42.4. Input¶

The complexity inherit in a discrete solvent model engenders a, potentially, complex input. To (hopefully) make the input transparent the set of keywords are ordered in several tiers. Below all keywords and their sub- and subsubkeywords are presented. A keyword with several tiers should typically be of the following form

```
SIMUlation
...(keywords on higher tier)
END simulation
```

Also consult the input example below and the examples in section 5.1.6 for guidance. Mandatory keywords are highlighted.

- TITLe
- Title to the calculation.
- SIMUlation
Keywords relating to the how the simulation is to be performed and under which conditions.

**RADIus**Initial radius of the dielectric cavity. The radius is also specified on the startfile and has higher priority than the radius given with the present keyword.**PERMittivity**Permittivity of the dielectric continuum. 80 on default.**TEMPerature**Temperature in Kelvin. Default is 300.**PRESsure**Macroscopic pressure in atmosphere. Default is 1 atm.**SURFace**Surface tension parameter for the cavity. Default is for air–water interface.**TRANslation**Maximal translation in the simulation (in a.u.) Default is 0.0 a.u.**ROTAtion**Maximal angle for rotation of solvent around molecular axes. Default is 0°.**CAVIty**Maximal modification of radius of dielectric cavity. Default is 0.0 a.u.**FORCe**Force constant for the harmonic potential that presents a bias in the simulation for configurations with the QM-region close to the center of the cavity. Default is 0.001.**BREPulsion**Parameter for the Repulsion energy that keeps the QM-region away from the boundary. Default is 0.0 a.u.**SEED**Seed to the pseudo-random number generator.**PARAlleltemp**A parallel tempering procedure is performed to boost sampling. It is mainly used in systems with small transition elements in the Markov chain, which will give difficult samplings. Three lines follow: First line gives the number of different temperatures to perform the simulation, \(N_{\text{Temp}}\). In the second line \(N_{\text{Temp}}\) integers are given, each of these specify a file to store the configuration for each temperature. Third line gives the \(N_{\text{Temp}}\) temperatures used for the tempering procedure.**END_Simulation Parameters**Marks the end of the input to the simulation parameters.

- THREshold
- Followed by three numbers. First the threshold for the induced dipoles in the generalized self-consistent field method for the solution of the mutual polarization problem is specified. Second the the threshold for the energy in the same method is given. Finally the maximum number of iterations in the method is specified. Defaults are 0.0001 0.0000001 and 30.
- STEPs
- Followed by two entries. Number of macrosteps and number of microsteps. The total number of steps is the product of the two numbers above. At the end of each macrostep the relevant STFIL is up-dated. Default is 1 and 1.
- RUN
- Specify type of simulation. “QMEQ” means quantum chemical equilibration; only the startfile is up-dated. “QMPR” means quantum chemical production; startfile is up-dated and sampfile constructed. {bf Observe} that if “QMPR” is specified a line with two entries follows in which the interval of sampling is specified and on which sampfile (1-7) the data is to be stored. “ANAL” means an analysis of the stored results is to be performed.
- Print level. 1 is default and anything above this number can generate large outputs. No higher than 10 is recommended for non-developers.
- EXTErnal
- An external perturbation is to be added to the Hamiltonian in the Rassi alternative. The arguments are number of perturbation matrices, \(N\), followed by \(N\) lines. Each line has the form: \(c_i\) a scalar with which the perturbation can be scaled, \(V_i\) is a character string with the label of the perturbation as given on SEWARD’s one-electron integral file, \(nc_i\) is the component number of the perturbation. A final expression for the perturbation would be: \(c_1V_1(nc_1)+c_2V_2(nc_2)+\cdots+c_NV_N(nc_N)\).
- CONFiguration
Keywords relating to from which source the initial solvent configuration is to be obtained.

*It is mandatory to specify a source.***ADD**Followed by one number specifying how many solvent molecules that are to be added at random to the cavity. This is the worst way to start a simulation since it will take a lot of time to equilibrate the system.**FILE**Signify that start configuration is to be read from some file.**STARtfile**Read solvent configuration from startfile.**SCRAtch**Read solvent configuration from startfile and place the QM-region as given on RUNFILE.**COPY**Read solvent and QM configuration from startfile. This is he keyword to use if a simulation is to be restarted.**Observe**that consistent startfile and RUNFILE must be used.**CM_,_**Read solvent configuration from startfile and place the QM in the center of mass of the QM placed on startfile. For any of the previous keywords two numbers are given, \(N_{\text{in}}\) and \(N_{\text{out}}\) which specify from which startfile QMSTAT is supposed to read and write, respectively

**SAMPfile**Read solvent configurations put on a sampfile and analyze them. Two numbers are given, \(N_{\text{in}}\) and \(N_{\text{extr}}\) which specify from which sampfile QMSTAT is supposed to read and on which extract file the results are to be put.

**INPUt**The starting configuration is to be read from the input. The coordinates are given after the keyword COORdinates in the second tier to the SOLVent keyword. One number as argument: the startfile to which configurations are written.**END_Configuration**Marks the end of the input to the initial configuration.

- EDIT
Signify that a startfile is to be edited. If this keyword is given, then no simulation will be performed.

**DELEte**Two rows follow; on the first \(N_{\text{in}}\) and \(N_{\text{out}}\) are given which specify the startfile to read from and write to, respectively; on the second the number of solvent molecules to delete. The solvent molecules farthest away from origin are deleted.**ADD**The form of the arguments as DELEte above, only the second row give number of molecules to add.**Observe**that the keyword RADIus will with the present keyword specified give the radius of the cavity of the edited startfile.**QMDElete**Delete the QM-region and substitute it by water molecules. One row follows with two numbers, which specify the startfile to read from and write to, respectively.**DUMP**Dump startfile coordinates in a way suitable for graphical display. Two rows follow; on the first a character string with the format the coordinated will be dumped; on the second \(N_{\text{in}}\) specifies the startfile to read. Currently there is only one format for this keyword: MOLDen.**END_EditStartFile**Marks the end of the input to edit the startfile.

- QMSUrrounding
Keywords that are related to the interaction between surrounding and the quantum chemical region.

**DPARameters**Parameters for the dispersion interaction. Follow \(N\) lines, which \(N\) the number of atoms in the QM-region. The general form for each line is: \(d_1\) and \(d_2\) where \(d_1\) is the dispersion parameter between one atom of the QM-region and the water oxygen, and \(d_2\) is the same but regarding to the hydrogen of the water.The order of the QM atoms is given by RUNFILE.**ELECtrostatic**Parameters to describe the electrostatic penetration using Slater integrals.**THREsholds**Two number follow. First, the cutoff (distance Quantum Site-Classical molecule) to evaluate penetration effects. Default is 6 a.u. Second, difference between two Slater exponents to not be consider the same value. Default is 0.001.**NOPEnetration**No electric penetration is considered in the calculations. Penetration is considered by default.**QUADrupoles**Electrostatic Penetration computed in quadrupoles. Default is that penetration is computed up to dipoles.**END Electrostatic**Marks the end of the input to the electrostatic penetration computed by Slater.

**XPARameters**Parameters to describe the repulsion energy.**S2**The parameter for the \(\sim S^2\) term. Default zero.**S4**The parameter for the \(\sim S^4\) term. Default zero.**S6**The parameter for the \(\sim S^6\) term. Default zero.**S10**The parameter for the \(\sim S^{10}\) term. Default zero.**CUTOff**Two numbers follow. The first is the cut-off radius such as if any distance from the given solvent molecule is longer than this number, the overlap term is set to zero. The second is a cut-off radius such as if any distance from the given solvent molecule is shorter than this number the energy is set to infinity, or practically speaking, this configuration is rejected with certainty. Defaults are 10.0 a.u.~and 0.0 a.u.**END XParameters**Marks the end of the input to the repulsive parameters.

**DAMPing****DISPersion**Input parameters to a dispersion damping expression. The parameters are number obtain from a quantum chemical calculation. All lines have the form: \(C_{\text{val}}\), \(Q_{xx}\), \(Q_{yy}\), \(Q_{zz}\) where \(C_{\text{val}}\) is the valence charge and \(Q_{**}\) are diagonal terms in the quadrupole tensor. First two lines are for the hydrogen atom then the oxygen atom in a water molecule. Next follows as many lines as atoms in the QM region. All these quantities can be obtained from a calculation with MPPROP. The numbers are given as input so that the user can if it is found to be needed, modify the damping. Default is no damping. The order of the atoms in the QM region is given by RUNFILE.**FIELd**The electric field between QM region and surrounding is damped. Three numbers are arguments:\(C_{\text{O}}\), \(C_{\text{H}}\), \(N\) where they are parameters to a field damping expression (\(E=\tilde{E}(1-e^{C_x R})^N\)) where \(x\) is \(\text{O}\) if the point in the surrounding is on a oxygen atom, \(\text{H}\) if on a hydrogen atom; \(R\) is the distance between the point in the QM region and the points in the surrounding.**END Damping**Marks the end of the input to the Damping parameters.

**END QmSurrounding**Marks the end of the input related to the interaction between surrounding and the quantum chemical region.

- SOLVent
Keywords that govern the solvent-solvent interaction and some other initial data. Most of these numbers are presently fixed and should not be altered.

**COORdinates**If solvent coordinates are to be given explicitly in input. First line gives number of particles to add. Then follows three times that number lines with coordinates for the oxygen atom and the hydrogen atoms. If the keyword SINGle-point has been given the present keyword assumes a different meaning (see description of SINGle-point).**CAVRepulsion**Two parameters that regulate the repulsion with the boundary of the cavity. Defaults are 30.0 and 0.06.**ATCEchpol**Five numbers follow: number of atoms, centers, charges, polarizabilities and slater sites. Defaults are 3, 5, 4, 3 and 5, respectively.**CHARge**Four numbers follow: the partial charge on the hydrogen atoms and the partial charge on the pseudo-centers.**POLArizability**Three numbers follow: the polarizability on the oxygen atom and on the two hydrogen atoms.**SLATer**Magnitude of Slater Prefactors and exponents. One mumber follow: 0 is slater description of electrostatics up to charges, 1 up to dipoles. Then it follows N times (where N is the number of Slater centers) three lines if description up to charge. First line Slater exponent for charges, second line Slater Prefactor and third line nuclear charge of the center. If the description goes up to dipole, N times five lines follows. First two lines are the same as charge description, third line is Slater exponent for dipole, fourth line is the three Slater Prefactors for the dipole (one for each cartesian coordinate) and fith line is the nuclear charge of the center. Defaults: See papers of Karlstrom. If the number of Slater sites is modified this keyword should be after ATCEchpol**END Solvent**Marks the end of the input that govern the solvent-solvent interaction.

- RASSisection
This section provides the information needed to perform QMSTAT calculations using the RASSI-construction of the wave function.

**JOBFiles**First number give the number of JOB-files that was generated by RASSCF (i.e., how many RASSCF calculations that preceded QMSTAT). The following numbers (as many as the number of JOB-files) specify how many states each calculation rendered. So for example if a State-Average (SA) RASSCF calculation is performed with two states, the number should be 2.**EQSTate**Which state interacts with the surrounding. Should be 1 if it is the ground state, which also is the default.**MOREduce**A Reduction of the Molecular Orbitals is performed. One number as argument: the threshold giving the value of the lowest occupation number of the selected natural orbitals [102].**CONTract**The RASSI state basis are contracted. One number as argument: the threshold giving the value of the lowest RASSCF overlap for the RASSI state basis [102].**LEVElshift**Introduce levelshift of RASSI states. Three lines must be written. First line gives the number of levelshifts to perform. Then follows the states to levelshift (as many as the number of levelshifts). Finally, the value of the levelshift for each state is given.**CISElect**The QM solvent overlap is used as the criterion to choose the state that interacts with the surrounding. Three lines follow. One entire: among how many states can be chosen the interacting state, \(N\). The second line, \(N\) entries giving the number of each state. Finally, \(N\) scaling factors, one for each state, of the overlap.**END RassiSection**Marks the end of the input that govern the Rassi calculations.

- SCFSection
This section provides additional information to perform QMSTAT calculations using the SCF-construction of the wave function.

**ORBItals**Two numbers are required: how many orbitals that are to be used how many occupied orbitals there are in the QM region. as a basis in which to solve the Hartree-Fock equation, and**END ScfSection**Marks the end of the input that govern the Scf calculations.

- SINGle-point
- This keywords signals that a set of single point calculations
should be performed; this is typically what one needs when
fitting parameters. The keyword gives the COORdinates
keyword in the SOLVent section a new meaning. The first
row then gives the number of points in which a single-point calculation
should be performed and the coordinates that follow give the
coordinates for the water monomer. QMSTAT then run each
solute-monomer solvent configuration specified and the energy (among
other things) is computed. The keyword
thus overrides
the usual meaning of the input.
**Observe**that the permittivity has to be set to 1 if one attempts to reproduce a quantum chemical supermolecular potential. - EXTRact Section
Give details about the analysis performed to the results stored in the sampfile.

**TOTAl energy**The total energy of the whole system is extracted.**DIPOle**The three components and the total dipole of the QM-region are extracted.**QUADrupole**The six components and the quadrupole of the QM-region are extracted.**EIGEn**The Eigenvalues of the RASSI matrix and the eigenvectors are extracted. Follow by a number and a “YES” or “NON” statement. The number gives the highest state where the eigenvalue is extracted. YES means that also the corresponding eigenvectors are extracted.**EXPEctation values**The expectation values of \(H_0\) and main perturbations: \(V_{\text{el}}\), \(V_{\text{pol}}\) and \(V_{\text{n}-\text{el}}\) are extracted. If keyword EIGEn is specified it is done for the same states as this keyword, otherwise the extraction is performed for the equilibrated state.**Observe**that the expectation values are for the final wave function of the QM-region in solution, so \(H_0\) is not the same as for the isolated QM-region.**ELOCal**The local expectation values of \(V_{\text{el}}\) and \(V_{\text{pol}}\) for the multipole expansion sites are extracted. Two lines follow. First, gives for how many sites these values will be extracted, \(N\). Second line, \(N\) entries giving the number of each site. If keyword EIGEn is specified the extraction is done for the same states as this keyword, otherwise it is performed for the equilibrated state.**MESP**The Main Electrostatic potential, field and field gradients will be obtained in order to produce perturbation integrals that will be used to optimize the intramolecular geometry of the QM system.**Observe**that this keyword will change the one electron integrals file, so it is advised to make a copy of the original file. After running this option ALASKA and SLAPAF must be running with the new one electron integrals file in order to produce the gradients and a new geometry in the geometry optimization procedure.**END ExtractSection**Marks the end of the input that give details about the analysis performed.

### 4.2.42.4.1. Input example¶

The following input uses the Rassi alternative and restarts from startfile.0 and write to startfile.1 every 1000th step, where the total number of steps is 200*1000. A set of parameters are given which are for an organic molecule with one carbon, one oxygen and two hydrogen atoms. The order in the previous SEWARD and RASSCF calculations for the atoms is carbon, oxygen, hydrogen 1 and hydrogen 2. The dispersion is damped. Finally, there are sixteen RASSCF calculations preceeding and the last two are state-average since two states are collected from these files; the ground state interacts with the surrounding.

```
&QmStat &End
Simulation * Simulation parameters.
Translation
0.03 * Maximun translation step of water.
Rotation
1.0 * Maximun rotation step of water.
Cavity
0.05 * Maximun variation of the cavity radius for step.
End Simulation
Steps * Number of macro and microsteps.
200 1000
Configuration * How the start configuration is readed.
Start * The cordinates are taken form a startfile.
Copy * The coordinates of the QM region are the same as in the startfile.
0 1
End Configuration
QmSurrounding
DParameters * Dispersion parameters.
35.356 4.556 * Carbon_{QM}-Oxygen_{wat} Carbon_{QM}-Hydrogen_{wat}.
16.517 2.129 * Oxygen_{QM}-Oxygen_{wat} Oxygen_{QM}-Hydrogen_{wat}.
10.904 1.405 * Hydrogen1_{QM}-Oxygen_{wat} Hydrogen1_{QM}-Hydrogen_{wat}.
10.904 1.405 * Hydrogen2_{QM}-Oxygen_{wat} Hydrogen2_{QM}-Hydrogen_{wat}.
XParameters * QM-Solvent Repulsion Parameters.
S2
-0.375
S6
1.7
End XParameters
Damping * Dispersion Damping.
Dispersion
-6.64838476 -5.22591434 -4.32517889 -4.58504467 * Water Hydrogen.
-.34146881 -0.21833165 -0.22092206 -0.21923063 * Water Oxygen.
-4.23157193 -1.91850438 -2.28125523 -1.91682521 * Quamtum Carbon.
-6.19610865 -3.90535461 -4.73256142 -3.77737447 * Quantum Oxygen.
-.57795931 -0.42899268 -0.43228880 -0.43771290 * Quantum Hydrogen 1.
-.57795931 -0.42899268 -0.43228880 -0.43771290 * Quantum Hydrogen 2.
End Damping
End QmSurrounding
RassiSection
JobFiles * Number of JobFiles.
16
1 1 1 1 1 1 1 1 1 1 1 1 1 1 2 2 * One state is collected form all JobFiles
* except from the two last ones, which two
* are collected.
EqState * The state interacting with the surrounding.
1
End RassiSection
End of Input
```