# Release62:ONIOM

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- | geometry # Note cannot use full D3D symmetry here | + | geometry # Note cannot use full D3D symmetry here, either specify noautosym or change atom tag |

H -0.72023641 0.72023641 -1.16373235 | H -0.72023641 0.72023641 -1.16373235 | ||

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H -0.98386124 -0.26362482 1.16373235 | H -0.98386124 -0.26362482 1.16373235 | ||

H 0.26362482 0.98386124 1.16373235 | H 0.26362482 0.98386124 1.16373235 | ||

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===Optimization and frequencies=== | ===Optimization and frequencies=== |

## Latest revision as of 17:58, 24 June 2014

## Contents |

# Hybrid Calculations with ONIOM

ONIOM is the hybrid method of Morokuma and co-workers that enables different levels of theory to be applied to different parts of a molecule/system and combined to produce a consistent energy expression. The objective is to perform a high-level calculation on just a small part of the system and to include the effects of the remainder at lower levels of theory, with the end result being of similar accuracy to a high-level calculation on the full system.

- M. Svensson, S. Humbel, R.D.J. Froese, T. Mastubara, S. Sieber, and K. Morokuma, J. Phys. Chem., 100, 19357 (1996).
- S. Dapprich, I. Komaromi, K.S. Byun, K. Morokuma, and M.J. Frisch, J. Mol. Struct. (Theochem), 461-462, 1 (1999).
- R.D.J. Froese and K. Morokuma in ``Encylopedia of Computational Chemistry,
*volume 2, pp.1244-1257, (ed. P. von Rague Schleyer, John Wiley and Sons, Chichester, Sussex, 1998).*

The NWChem ONIOM module implements two- and three-layer ONIOM models for use in energy, gradient, geometry optimization, and vibrational frequency calculations with any of the pure quantum mechanical methods within NWChem. At the present time, it is not possible to perform ONIOM calculations with either solvation models or classical force fields. Nor is it yet possible to compute properties except as derivatives of the total energy.

Using the terminology of Morokuma et al., the full molecular geometry including all atoms is referred to as the "real" geometry and it is treated using a "low"-level of theory. A subset of these atoms (referred to as the "model" geometry) are treated using both the "low"-level and a "high"-level of theory. A three-layer model also introduces an "intermediate" model geometry and a "medium" level of theory.

The two-layer model requires a high and low level of theory and a real and model molecular geometry. The energy at the high-level of theory for the real geometry is estimated as

E(High,Real) = E(Low,Real) + [E(High,Model) - E(Low,Model)].

The three-layer model requires high, medium and low levels of theory, and real, intermediate and model geometries and the corresponding energy estimate is

E(High,Real) = E(Low,Real) + [E(High,Model) - E(Medium,Model)] + [E(Medium,Inter) - E(Low,Inter)].

When does ONIOM work well? The approximation for a two-layer model will be good if

- the model system includes the interactions that dominate the energy difference being computed and the high-level of theory describes these to the required precision, and
- the interactions between the model and the rest of the real system (substitution effects) are described to sufficient accuracy at the lower level of theory.

ONIOM is used to compute energy differences and the absolute energies are not all that meaningful even though they are well defined. Due to cancellation of errors, ONIOM actually works better than you might expect, but a poorly designed calculation can yield very bad results. Please read and heed the caution at the end of the article by Dapprich et al.

The input options are as follows

ONIOM HIGH <string theory> [basis <string basis default "ao basis">] \ [ecp <string ecp>] [input <string input>] [MEDIUM <string theory> [basis <string basis default "ao basis">] \ [ecp <string ecp>] [input <string input>]] LOW <string theory> [basis <string basis default "ao basis">] \ [ecp <string ecp>] [input <string input>] MODEL <integer natoms> [charge <double charge>] \ [<integer i1 j1> <real g1> [<string tag1>] ...] [INTER <integer natoms> [charge <double charge>] \ [<integer i1 j1> <real g1> [<string tag1>] ...]] [VECTORS [low-real <string mofile>] [low-model <string mofile>] \ [high-model <string mofile>] [medium-model <string mofile]\ [medium-inter <string mofile>] [low-inter <string mofile>]] [PRINT ...] [NOPRINT ...] END

which are described in detail below.

For better validation of user input, the HIGH, LOW and MODEL directives must always be specified. If the one of the MEDIUM or INTER directives are specified, then so must the other.

## Real, model and intermediate geometries

The geometry and total charge of the full or real system should be specified as normal using the geometry directive. If *N*_{model} of the atoms are to be included in the model system, then these should be specified first in the geometry. Similarly, in a three-layer calculation, if there are *N*_{inter} atoms to be included in the intermediate system, then these should also be arranged together at the beginning of the geometry. The implict assumption is that the model system is a subset of the intermediate system which is a subset of the real system. The number of atoms to be included in the model and intemediate systems are specified using the MODEL and INTER directives. Optionally, the total charge of the model and intermediate systems may be adjusted. The default is that all three systems have the same total charge.

Example 1. A two-layer calculation on *K*^{ + }(*H*_{2}*O*) taking the potassium ion as the model system. Note that no bonds are broken so no link atoms are introduced. The real geometry would be specified with potassium (the model) first.

geometry autosym K 0 0.00 1.37 O 0 0.00 -1.07 H 0 -0.76 -1.68 H 0 0.76 -1.68 end

and the following directive in the ONIOM input block indicates that one atom (implicitly the first in the geometry) is in the model system

model 1

### Link atoms

Link atoms for bonds spanning two regions are automatically generated from the bond information. The additional parameters on the MODEL and INTER directives describe the broken bonds including scale factors for placement of the link atom and, optionally, the type of link atom. The type of link atom defaults to hydrogen, but any type may be specified (actually here you are specifying a geometry tag which is used to associate a geometrical center with an atom type and basis sets, etc. For each broken bond specify the numbers of the two atoms (i and j), the scale factor (g) and optionally the tag of the link atom. Link atoms are placed along the vector connecting the the first to the second atom of the bond according to the equation

where *g* is the scale factor. If the scale factor is one, then the link atom is placed where the second atom was. More usually, the scale factor is less than one, in which case the link atom is placed between the original two atoms. The scale factor should be chosen so that the link atom (usually hydrogen) is placed near its equilibrium bond length from the model atom. E.g., when breaking a single carbon-carbon bond (typical length 1.528 Angstrøms) using a hydrogen link atom we will want a carbon-hydrogen bond length of about 1.084 Angstrøms, so the scale factor should be chosen as 1.084/1.528 ~ 0.709.

Example 2. A calculation on acetaldehyde (*H*_{3}*C* − *C**H**O*) using aldehyde (*H* − *C**H**O*) as the model system. The covalent bond between the two carbon atoms is broken and a link atom must be introduced to replace the methyl group. The link atom is automatically generated -- all you need to do is specify the atoms in the model system that are also in the real system (here *C**H**O*) and the broken bonds. Here is the geometry of acetaldehyde with the *C**H**O* of aldehyde first

geometry C -0.383 0.288 0.021 H -1.425 0.381 0.376 O 0.259 1.263 -0.321 H 0.115 -1.570 1.007 H -0.465 -1.768 -0.642 H 1.176 -1.171 -0.352 C 0.152 -1.150 0.005 end

There are three atoms (the first three) of the real geometry included in the model geometry, and we are breaking the bond between atoms 1 and 7, replacing atom 7 with a hydrogen link atom. This is all accomplished by the directive

model 3 1 7 0.709 H

Since the default link atom is hydrogen there is actually no need to specify the ``H*.*

See also the three-layer example for a more complex example.

### Numbering of the link atoms

The link atoms are appended to the atoms of the model or intermediate systems in the order that the broken bonds are specified in the input. This is of importance only if manually constructing an initial guess.

## High, medium and low theories

The two-layer model requires both the high-level and low-level theories be specified. The three-layer model also requires the medium-level theory. Each of these includes a theory (such as SCF, MP2, DFT, CCSD, CCSD(T), etc.), an optional basis set, an optional ECP, and an optional string containing general NWChem input.

### Basis specification

The basis name on the theory directive (high, medium, or low) is that specified on a basis set directive (see Section 7) and not the name of a standard basis in the library. If not specified, the basis set for the high-level theory defaults to the standard "ao basis". That for the medium level defaults to the high-level basis, and the low-level basis defaults to the medium-level basis. Other wavefunction parameters are obtained from the standard wavefunction input blocks. See Effective core potential for an example.

### Effective core potentials

If an effective core potential is specified in the usual fashion outside of the ONIOM input then this will be used in all calculations. If an alternative ECP name (the name specified on the ECP directive in the same manner as done for basis sets) is specified on one of the theory directives, then this ECP will be used in preference for that level of theory. See teh three-layer example for sample input.

### General input strings

For many purposes, the ability to specify the theory, basis and effective core potential is adequate. All of the options for each theory are determined from their independent input blocks. However, if the same theory (e.g., DFT) is to be used with different options for the ONIOM theoretical models, then the general input strings must be used. These strings are processed as NWChem input each time the theoretical model is invoked. The strings may contain any NWChem input, except for options pertaining to ONIOM and the task directive. The intent that the strings be used just to control the options pertaining to the theory being used.

A word of caution. Be sure to check that the options are producing the desired results. Since the NWChem database is persistent and the ONIOM calculations happen in an undefined order, the input strings should fully define the calculation you wish to have happen.

For instance, if the high model is DFT/B3LYP/6-311g** and the low model is DFT/LDA/3-21g, the ONIOM input might look like this

oniom model 3 low dft basis 3-21g input "dft\; xc\; end" high dft basis 6-311g** input "dft\; xc b3lyp\; end" end

The empty XC directive restores the default LDA exchange-correlation option (see Section 11.3). Note that semi-colons and other quotation marks inside the input string must be preceded by a backslash to avoid special interpretation.

See |DFT with and without charge fitting for another example.

## Use of symmetry

Symmetry should work just fine as long as the model and intermediate regions respect the symmetry -- i.e., symmetry equivalent atoms need to be treated equivalently. If symmetry equivalent atoms must be treated in separate regions then the symmetry must be lowered (or completely switched off).

## Molecular orbital files

The VECTORS directive in the ONIOM block is different to that elsewhere in NWChem. For each of the necessary combinations of theory and geometry you can specify a different file for the molecular orbitals. By default each combination will store the MO vectors in the permanent directory using a file name created by appending to the name of the calculation the following string

- low-real -- ".lrmos"
- low-inter -- ".limos"
- low-model -- ".lmmos"
- medium-inter -- ".mimos"
- medium-model -- ".mmmos"
- high-model -- ".hmmos"

Each calculation will utilize the appropriate vectors which is more efficient during geometry optimizations and frequency calculations, and is also useful for the initial calculation. In the absence of existing MO vectors files, the default atomic guess is used (see |Input/output of MO vectors).

If special measures must be taken to converge the initial SCF, DFT or MCSCF calculation for one or more of the systems, then initial vectors may be saved in a file with the default name, or another name may be specified using the VECTORS directive. Note that subsequent vectors (e.g., from a geometry optimization) will be written back to this file, so take a copy if you wish to preserve it. To generate the initial guess for the model or intermediate systems it is necessary to generate the geometries which is most readily done, if there are link atoms, by just running NWChem on the input for the ONIOM calculation on your workstation. It will print these geometries before starting any calculations which you can then terminate.

E.g., in a calculation on Fe(III) surrounded by some ligands, it is hard to converge the full (real) system from the atomic guess so as to obtain a *d*^{5} configuration for the iron atom since the *d* orbitals are often nominally lower in energy than some of the ligand orbitals. The most effective mechanism is to converge the isolated Fe(III) and then to use the fragment guess as a starting guess for the real system. The resulting converged molecular orbitals can be saved either with the default name (as described above in this section), in which case no additional input is necessary. If an alternative name is desired, then the VECTORS directive may be used as follows

vectors low-real /u/rjh/jobs/fe_ether_water.mos

## Restarting

Restart of ONIOM calculations does not currently work as smoothly as we would like. For geometry optimizations that terminated gracefully by running out of iterations, the restart will work as normal. Otherwise, specify in the input of the restart job the last geometry of the optimization. The Hessian information will be reused and the calculation should proceed losing at most the cost of one ONIOM gradient evaluation. For energy or frequency calculations, restart may not currently be possible.

## Examples

### Hydrocarbon bond energy

A simple two-layer model changing just the wavefunction with one link atom.

This reproduces the two-layer ONIOM (MP2:HF) result from Dapprich et al. for the reaction *R* − *C**H*_{3} = *R* − *C**H*_{2} + *H* with *R* = *C**H*_{3} using *C**H*_{4} as the model. The geometries of *R* − *C**H*_{3} and *R* − *C**H*_{2} are optimized at the DFT-B3LYP/6-311++G** level of theory, and then ONIOM is used to compute the binding energy using UMP2 for the model system and HF for the real system. The results, including MP2 calculations on the full system for comparison, are as given in the table below.

Theory | Me-CH2 | Me-Me | H | De(Hartree) | De(kcal/mol) |

B3LYP | -79.185062 | -79.856575 | -0.502256 | 0.169257 | 106.2 |

HF | -78.620141 | -79.251701 | -0.499817 | 0.131741 | 82.7 |

MP2 | -78.904716 | -79.571654 | -0.499817 | 0.167120 | 104.9 |

MP2:HF | -78.755223 | -79.422559 | -0.499817 | 0.167518 | 105.1 |

The following input first performs a calculation on *C**H*_{3} − *C**H*_{2}, and then on *C**H*_{3} − *C**H*_{3}. Note that in the second calculation we cannot use the full symmetry since we are breaking the C-C bond in forming the model system (the non-equivalence of the methyl groups is perhaps more apparent if we write *R* − *C**H*_{3}).

start basis spherical H library 6-311++G**; C library 6-311++G** end title "ONIOM Me-CH2" geometry autosym H -0.23429328 1.32498565 0.92634814 H -0.23429328 1.32498565 -0.92634814 C -0.13064265 0.77330370 0.00000000 H -1.01618703 -1.19260361 0.00000000 H 0.49856072 -1.08196901 -0.88665533 H 0.49856072 -1.08196901 0.88665533 C -0.02434414 -0.71063687 0.00000000 end scf; uhf; doublet; thresh 1e-6; end mp2; freeze atomic; end oniom high mp2 low scf model 3 3 7 0.724 end task oniom title "ONIOM Me-Me" geometry # Note cannot use full D3D symmetry here, either specify noautosym or change atom tag H -0.72023641 0.72023641 -1.16373235 H 0.98386124 0.26362482 -1.16373235 H -0.26362482 -0.98386124 -1.16373235 C 0.00000000 0.00000000 -0.76537515 H 0.72023641 -0.72023641 1.16373235 H -0.98386124 -0.26362482 1.16373235 H 0.26362482 0.98386124 1.16373235 C1 0.00000000 0.00000000 0.76537515 end scf; rhf; singlet; end oniom high mp2 low scf model 4 4 8 0.724 end task oniom

### Optimization and frequencies

A two-layer model including modification of theory, basis, ECP and total charge and no link atoms.

This input reproduces the ONIOM optimization and vibrational frequency calculation of *R**h*(*C**O*)_{2}*C**p* of Dapprich et al. The model system is . The low theory is the Gaussian LANL2MB model (Hay-Wadt n+1 ECP with minimal basis on Rh, STO-3G on others) with SCF. The high theory is the Gaussian LANL2DZ model (another Hay-Wadt ECP with a DZ basis set on Rh, Dunning split valence on the other atoms) with DFT/B3LYP. Note that different names should be used for the basis set and ECP since the same mechanism is used to store them in the database.

start ecp LANL2DZ_ECP rh library LANL2DZ_ECP end basis LANL2DZ spherical rh library LANL2DZ_ECP o library SV_(Dunning-Hay); c library SV_(Dunning-Hay); h library SV_(Dunning-Hay) end ecp Hay-Wadt_MB_(n+1)_ECP rh library Hay-Wadt_MB_(n+1)_ECP end # This is the minimal basis used by Gaussian. It is not the same # as the one in the EMSL basis set library for this ECP. basis Hay-Wadt_MB_(n+1) spherical Rh s; .264600D+01 -.135541D+01; .175100D+01 .161122D+01; .571300D+00 .589381D+00 Rh s; .264600D+01 .456934D+00; .175100D+01 -.595199D+00; .571300D+00 -.342127D+00 .143800D+00 .410138D+00; .428000D-01 .780486D+00 Rh p; .544000D+01 -.987699D-01; .132900D+01 .743359D+00; .484500D+00 .366846D+00 Rh p; .659500D+00 -.370046D-01; .869000D-01 .452364D+00; .257000D-01 .653822D+00 Rh d; .366900D+01 .670480D-01; .142300D+01 .455084D+00; .509100D+00 .479584D+00 .161000D+00 .233826D+00 o library sto-3g; c library sto-3g; h library sto-3g end charge 0 geometry autosym rh 0.00445705 -0.15119674 0.00000000 c -0.01380554 -1.45254070 1.35171818 c -0.01380554 -1.45254070 -1.35171818 o -0.01805883 -2.26420212 2.20818932 o -0.01805883 -2.26420212 -2.20818932 c 1.23209566 1.89314720 0.00000000 c 0.37739392 1.84262319 -1.15286640 c -1.01479160 1.93086461 -0.70666350 c -1.01479160 1.93086461 0.70666350 c 0.37739392 1.84262319 1.15286640 h 2.31251453 1.89903673 0.00000000 h 0.70378132 1.86131979 -2.18414218 h -1.88154273 1.96919306 -1.35203550 h -1.88154273 1.96919306 1.35203550 h 0.70378132 1.86131979 2.18414218 end dft; grid fine; convergence gradient 1e-6 density 1e-6; xc b3lyp; end scf; thresh 1e-6; end oniom low scf basis Hay-Wadt_MB_(n+1) ecp Hay-Wadt_MB_(n+1)_ECP high dft basis LANL2DZ ecp LANL2DZ_ECP model 5 charge 1 print low end task oniom optimize task oniom freq

### A three-layer example

A three layer example combining CCSD(T), and MP2 with two different quality basis sets, and using multiple link atoms.

The full system is tetra-dimethyl-amino-ethylene (TAME) or (N(Me)2)2-C=C-(N(Me)2)2. The intermediate system is (NH2)2-C=C-(NH2)2 and H2C=CH2 is the model system. CCSD(T)+aug-cc-pvtz is used for the model region, MP2+aug-cc-pvtz for the intermediate region, and MP2+aug-cc-pvdz for everything.

In the real geometry the first two atoms (C, C) are the model system (link atoms will be added automatically). The first six atoms (C, C, N, N, N, N) describe the intermediate system (again with link atoms to be added automatically). The atoms have been numbered using comments to make the bonding input easier to generate.

To make the model system, four C-N bonds are broken between the ethylene fragment and the dimethyl-amino groups and replaced with C-H bonds. To make the intermediate system, eight C-N bonds are broken between the nitrogens and the methyl groups and replaced with N-H bonds. The scaling factor could be chosen differently for each of the bonds.

start geometry C 0.40337795 -0.17516305 -0.51505208 # 1 C -0.40328664 0.17555927 0.51466084 # 2 N 1.87154979 -0.17516305 -0.51505208 # 3 N -0.18694782 -0.60488524 -1.79258692 # 4 N 0.18692927 0.60488318 1.79247594 # 5 N -1.87148219 0.17564718 0.51496494 # 6 C 2.46636552 1.18039452 -0.51505208 # 7 C 2.48067731 -1.10425355 0.46161675 # 8 C -2.46642715 -1.17982091 0.51473105 # 9 C -2.48054940 1.10495864 -0.46156202 # 10 C 0.30027136 0.14582197 -2.97072148 # 11 C -0.14245927 -2.07576980 -1.96730852 # 12 C -0.29948109 -0.14689874 2.97021079 # 13 C 0.14140463 2.07558249 1.96815181 # 14 H 0.78955302 2.52533887 1.19760764 H -0.86543435 2.50958894 1.88075113 ... and 22 other hydrogen atoms on the methyl groups end basis aug-cc-pvtz spherical C library aug-cc-pvtz; H library aug-cc-pvtz end basis aug-cc-pvdz spherical C library aug-cc-pvtz; H library aug-cc-pvtz end oniom high ccsd(t) basis aug-cc-pvtz medium mp2 basis aug-cc-pvtz low mp2 basis aug-cc-pvdz model 2 1 3 0.87 1 4 0.87 2 5 0.87 2 6 0.87 inter 6 3 7 0.69 3 8 0.69 4 11 0.69 4 12 0.69 \ 5 13 0.69 5 14 0.69 6 9 0.69 6 10 0.69 end task oniom

### DFT with and without charge fitting

Demonstrates use of general input strings.

A two-layer model for anthracene (a linear chain of three fused benzene rings) using benzene as the model system. The high-level theory is DFT/B3LYP/TZVP with exact Coulomb. The low level is DFT/LDA/DZVP2 with charge fitting.

Note the following.

- The semi-colons and quotation marks inside the input string must be quoted with backslash.
- The low level of theory sets the fitting basis set and the high level of theory unsets it.

start geometry symmetry d2h C 0.71237329 -1.21458940 0.0 C -0.71237329 -1.21458940 0.0 C 0.71237329 1.21458940 0.0 C -0.71237329 1.21458940 0.0 C -1.39414269 0.00000000 0.0 C 1.39414269 0.00000000 0.0 H -2.47680865 0.00000000 0.0 H 2.47680865 0.00000000 0.0 C 1.40340535 -2.48997027 0.0 C -1.40340535 -2.48997027 0.0 C 1.40340535 2.48997027 0.0 C -1.40340535 2.48997027 0.0 C 0.72211503 3.64518615 0.0 C -0.72211503 3.64518615 0.0 C 0.72211503 -3.64518615 0.0 C -0.72211503 -3.64518615 0.0 H 2.48612947 2.48094825 0.0 H 1.24157357 4.59507342 0.0 H -1.24157357 4.59507342 0.0 H -2.48612947 2.48094825 0.0 H 2.48612947 -2.48094825 0.0 H 1.24157357 -4.59507342 0.0 H -1.24157357 -4.59507342 0.0 H -2.48612947 -2.48094825 0.0 end basis small h library DZVP_(DFT_Orbital) c library DZVP_(DFT_Orbital) end basis fitting h library DGauss_A1_DFT_Coulomb_Fitting c library DGauss_A1_DFT_Coulomb_Fitting end basis big h library TZVP_(DFT_Orbital) c library TZVP_(DFT_Orbital) end oniom model 8 1 9 0.75 2 10 0.75 3 11 0.75 4 12 0.75 high dft basis big input "unset \"cd basis\"\; dft\; xc b3lyp\; end" low dft basis small input "set \"cd basis\" fitting\; dft\; xc\; end" end task oniom