Wavefunction Spartan Crack

Questions About Spectra:

Wave Function Spartan Crackers

What 'logP' models does Spartan provide?

The Villar method is available from semi-empirical calculations (with no d-orbitals). The Villar method examines the overlap matrix, searching for the type and number of lone pairs as well as the surface area of each atom; it is parameterized for H,C,N,O,F,S,Cl.
The reference is:
- Ibon Alkorta, Hugo O. Villar, Int. J. Quant. Chem. Vol. 44, 203-218 (1992)
- Angelina Kantola, Hugo O. Villar, Gilda H. Loew, J. Comp. Chem. vol. 12, No. 6, 681-689 (1991)

Ghose-Crippen is Spartan's default method for calculating logP. This method is independent of the energy/wavefunction. (i.e. one will get the same results from mechanics, semi-empirical, HF, DFT, and MP2 calculations). However, the Ghose-Crippen method is dependent on how the molecule is drawn/connected. The Ghose-Crippen method is parameterized for 110 atom/bonding types, including common bondings of H,C,N,O,S and the Halogens. For a test suite of 494 compounds, it provides a standard deviation of .347 and correlated coefficient of .962. In a test suite of 69 compounds beyond the original test suite it predicts a variance of .404.
The reference is:
- Ghose, Pritchett and Crippen J. Comput. Chem., 9, 80 (1988)

LogP can also be calculated directly from solvation energy. For example one can run a calculation with the POSTSOLVENT=SM12:1OCTANOL and then POSTSOLVENT=SM12:WATER keywords and use those energies in the equation LogP = [ SolvE_water - SolvE_1-octanol ] / 5.707 (all energies in kJ/mol; the 5.707 is log(10)*RT ) The solvation energy is printed in the output, or can be put into the spreadsheet by putting the following equation into a column header: SolvE = @energySolv*@hart2kj

'logP' methods can be selected with the LOGP= keyword;
LOGP=VILLAR and LOGP=GHOSE respectively.

An example Spartan file shows some of these logP examples on a broad range of simple molecules. While one can argue over which of these calculations is most precise or efficient, the noise in all these methods is typically better than the uncertainity in using LogP to predict common properties like blood/brain barriers.

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Spartan includes a number of ways to examine solvation.

C-PCM
The default solvation model which we advise for geometry and frequency calculations is the C-PCM model (Conductor like Polarizable continuum model). This depends on the shape and charge distribution of the molecule (solute) and the dielectric of the solvent.
Continuum models such as C-PCM do not account for explicit solvent-solute interactions such as hydrogen bonding or 'explicit hydrophobic'. For this reason we do not report an 'energy of solvation'.
Spartan gives easy access to three different dielectrics: 'NonPolar' (7.43 same as THF), 'Polar' (37.22, same as dimethylformamide), and 'Water' (78.3). From the pull-down menu in the Calculations dialogue. You can add another solvent by appending a dielectric constant or a solvent name, i.e.:
SOLVENT=CPCM:1BROMOPENTANE or
SOLVENT=CPCM:DIELECTRIC~10.3 (You can type the SOLVENT keyword in the option line, but when you hit return it will move to the pull-down menu.)
Some references for C-PCM models are:
- X. Zhang and J. M. Herbert, J. Phys. Chem. B118, 7806 (2014) 'Excited-State Deactivation Pathways in Uracil versus Hydrated Uracil: Solvatochromatic Shift in the ¹nπ^* State is the Key'
- A. W. Lange, J. M. Herbert, Chem. Phys. Lett.509 77-87 (2011) 'Symmetric versus asymmetric discretization of the integral equations in polarizable continuum solvation models'
- T. N. Truong and E. V. Stefanovich, Chem. Phys. Lett.240, 253 (1995)
- V. Barone and M. Cossi, J. Phys. Chem. A102, 1995 (1998)
C-PCM variations.
There is a large and diverse literature on C-PCM methods. Spartan's defaults should probably be used as these have been tested and are reasonable for organic systems. However for those familiar with the C-PCM literature we allow some access to the variations. There are 3 main 'methods' to treat the polarizable continuum. One can replace the CPCM in the SOLVENT= keyword above with
1. CPCM which uses a dielectric screening factor of f_e=(ε-1)/ε.
2. SSVPE which is a symmetrized version of an integral equation formalism (IEF-PCM) model with a screening factor of f_e=(ε-1)/(ε+1/2).
3. SMD is a Cramer-Trular SMx method which uses the CPCM formulation for the polarization term.
By appending SOLVENT=SSVPE:DIELECTRIC~10.3
SSVPE has been argued to be the best method for solvated excited states. an example of using SSVPE that might be appropriate for excited states is
ADDSOLVENT=SSVPE:DIETHYLETHER,STATESPECIFIC~PERTURB,CHARGESEPARATION~MARCUS (The ADDSOLVENT= is a pseudonym for SOLVENT= but this keyword stays in the Options line as opposed to popping over to the pull-down menu. This has the advantage of being able to more easily edit the line if needed.)
There are a number of other parameters which can be changed in C-PCM models which can be added as comma separated options appended to the keyword after the dielectric. These are:
- DIELECTRIC (If using a solvent name this is not required)
- OPTICALDIELECTRIC While formally required for excited state calculations we use an appropriate value if using a solvent name)
- TEMPERATURE
- PRESSURE
- SOLVENTRHO
- STATESPECIFIC
- CHARGESEPARATION
For a full list and more in depth discussion we follow the notation and keywords found in the Q-Chem 4.0 Manual.
Cramer-Truhlar SM5.4 solvation
We currently implement the Cramer-Truhlar SM5.4P and SM5.4A solvation methods for water, and is available to any molecule SM5 parameterized atoms.
This is a very fast method and is appropriate to get quick 'energy of solvation' energies at a given geometry. To use this model, for 'solvation energy' calculations use the SM54 keyword in the option line.
The energy of solvation predicted by this model can be found in the output text. You can print this in the spreadsheet with the equation
Solve.E.=@prop(SOLV_CORRECTION)*@hart2kj,
In Spartan '10 and Spartan '14 this calculation was done by default for all HF and DFT jobs.
Literature on these methods is extensive, some important articles are:
- Christopher J. Cramer, Donald G. Truhlar J. Comp. Chem.13, no. 9, 1089-1097 (1992) 'PM3-SM3: A General Parameterization for Including aqueous Solvation Effects in the PM3 Molecular Orbital Model'
- Candee C. Chambers, Gregory D. Hawkins, Christopher J. Cramer Donald G. Truhlar J. Phys. Chem.100, 16385-16398 (1996) 'Model for Aqueous Solvation Based on Class IV Atomic Charges and First Solvation Shell Effects'
MMFFaq mechanics force field (SM5.0R)
SM5.0R is a solvation method derived from the semi-empirical SM54 approach described above. It is independent of the wave function and depends only on the geometry of the molecule. As such, it is very fast and is applicable to large systems and molecular mechanics calculations. This method can be accessed by using the POSTSOLVENT=SM50R keyword.
MMFFaq is an extension to the MMFF94 forcefield, in which the SM50R energy term is added to the molecular mechanics energy. In Spartan, the MMFFaq force field is implemented such that the solvation energy is only added AFTER the geometry has been optimized. Thus the structures of molecules from MMFF94 and MMFFaq calculations will be the same, but their energies will be different. The MMFFaq method is most useful in the context of conformational searching or in an energy profile as the energy ordering of any conformers will likely be different in water (MMFFaq) than in vacuum (MMFF94).
The reference for SM5.0R is
- G.D. Hawkins, C.J. Cramer, D.G. Truhlar J. Phys. Chem. B101, 7147-7157 (1997) 'Parameterized Model for Aqueous Free Energies of Solvation using Geometry-dependent Atomic Surface Tensions with Implicit Electrostatics'
SM8, SM12 and SMD solvation calculation
The SM8 and SM12 model allow both water and a number of organic solvents and treats both neutral and charged solutes. This method is notable for the large suite of experimental data used to parameterize the model and uses the HF or DFT wave functions. To run SM8 as a property calculation (to calculate the energy of solvation) use the keyword POSTSOLVENT=SM8:WATER (and POSTSOLVENT=SM12 where water can be replaced with many different organic solvents. This method is dependent on the basis set, and is parameterized for the 6-31G* sets. (While the method will function for other variants in the 6-31G series, experience has shown that using larger basis sets worsens the results.
Technically, it is possible to do geometry optimizations with these models, but because of the discontinuous nature of the derivatives (due to the SCF like nature of solvated charge calculation) optimizations and frequency are problematic except for the simplest of molecules. Use the SOLVENT=SM12:WATER keyword for optimizations. (When you type in this keyword and hit 'enter'; the keyword will replace the 'in Gas' pull-down menu in the upper right of the Calculations dialogue.)
For SM8, SM12 and SMD you can use a number of different solvents in place of water. The list of supported solvents follows:
WATER, 111TRICHLOROETHANE, 112TRICHLOROETHANE, 11DICHLOROETHANE, 124TRIMETHYLBENZENE, 14DIOXANE, 1BROMO2METHYLPROPANE, 1BROMOPENTANE, 1BROMOPROPANE, 1BUTANOL, 1CHLOROPENTANE, 1CHLOROPROPANE, 1DECANOL, 1FLUOROOCTANE, 1HEPTANOL, 1HEXANOL, 1HEXENE, 1HEXYNE, 1IODOBUTANE, 1IODOPENTENE, 1IODOPROPANE, 1NITROPROPANE, 1NONANOL, 1OCTANOL, 1PENTANOL, 1PENTENE, 1PENTYNE, 1PROPANOL, 222TRIFLUOROETHANOL, 224TRIMETHYLPENTANE, 24DIMETHYLPENTANE, 24DIMETHYLPYRIDINE, 26DIMETHYLPYRIDINE, 2BROMOPROPANE, 2CHLOROBUTANE, 2HEPTANONE, 2HEXANONE, 2METHYLPENTANE, 2METHYLPYRIDINE, 2NITROPROPANE, 2OCTANONE, 2PENTANONE, 2PROPANOL, 2PROPEN1OL, 3METHYLPYRIDINE, 3PENTANONE, 4HEPTANONE, 4METHYL2PENTANONE, 4METHYLPYRIDINE, 5NONANONE, ACETICACID, ACETONE, ACETONITRILE, ANILINE, ANISOLE, BENZALDEHYDE, BENZENE, BENZONITRILE, BENZYLALCOHOL, BROMOBENZENE, BROMOETHANE, BROMOOCTANE, BUTANAL, BUTANOICACID, BUTANONE, BUTANONITRILE, BUTYLETHANOATE, BUTYLAMINE, BUTYLBENZENE, CARBONDISULFIDE, CARBONTET, CARBONTETRACHLORIDE, CCL4, CHLOROBENZENE, CHLOROTOLUENE, CIS12DIMETHYLCYCLOHEXANE, DECALIN CYCLOHEXANE, CYCLOHEXANONE, CYCLOPENTANE, CYCLOPENTANOL, CYCLOPENTANONE, DECANE, DIBROMOMETHANE, DIBUTYLETHER, DICHLOROMETHANE, DIETHYLETHER, DIETHYLSULFIDE, DIETHYLAMINE, DIIODOMETHANE, DIMETHYLDISULFIDE, DIMETHYLACETAMIDE, DIMETHYLFORMAMIDE, DMF, DIMETHYLPYRIDINE, DMSO, DIMETHYLSULFOXIDE, DIPROPYLAMINE, DODECANE, E12DICHLOROETHENE, TRANS12DICHLOROETHENE, E2PENTENE, ETHANETHIOL, ETHANOL ETHYLETHANOATE, ETHYLMETHANOATE, ETHYLPHENYLETHER, ETHYLBENZENE, ETHYLENEGLYCOL, FLUOROBENZENE, FORMAMIDE, FORMICACID, HEXADECYLIODIDE, HEXANOIC, IODOBENZENE, IODOETHANE, IODOMETHANE, ISOBUTANOL, ISOPROPYLETHER, ISOPROPYLBENZENE, ISOPROPYLTOLUENE, MCRESOL, MESITYLENE, METHANOL, METHYLBENZOATE, METHYLETHANOATE, METHYLMETHANOATE, METHYLPHENYLKETONE, METHYLPROPANOATE, METHYLBUTANOATE, METHYLCYCLOHEXANE, METHYLFORMAMIDE, MXYLENE, HEPTANE, HEXADECANE, HEXANE, NITROBENZENE, NITROETHANE, NITROMETHANE, METHYLANILINE, NONANE, OCTANE, PENTANE, OCHLOROTOLUENE, OCRESOL, ODICHLOROBENZENE, ONITROTOLUENE, OXYLENE, PENTADECANE, PENTANAL, PENTANOICACID, PENTYLETHANOATE, PENTYLAMINE, PERFLUOROBENZENE, PHENYLETHER, PROPANAL, PROPANOICACID, PROPANONITRILE, PROPYLETHANOATE, PROPYLAMINE, PXYLENE, PYRIDINE, PYRROLIDINE, SECBUTANOL, TBUTANOL, TBUTYLBENZENE, TETRACHLOROETHENE, THF, TETRAHYDROFURAN, TETRAHYROTHIOPHENEDIOXIDE, TETRALIN, THIOPHENE, THIOPHENOL, TOLUENE TRANSDECALIN, TRIBROMOMETHANE, TRIBUTYLPHOSPHATE, TRICHLOROETHENE, TRICHLOROMETHANE, TRIETHYLAMINE, UNDECANE, Z12DICHLOROETHENE
It is important to notice that no spaces are allowed in the name, thus 'acetic acid' is spelled 'ACETICACID'.
SM12 has been defined for multiple charge models. The default uses Charge Model 5 (CM5) but Merz-Singh-Kollman (MK) and ChElpG (CHELPG) charges are also available. You can access these by adding to the end of the POSTSOLVENT= keyword. For example:
POSTSOLVENT=SM12:1OCTANOL,CHARGES:chelpg
Some useful reference are
- A.V. Marenich, R.M. Olson, C.P. Kelly, C.J. Cramer, D.G. Truhlar, 'Self-Consistent Reaction Field Model for Aqueous and Nonaqueous Solutions Based on Accurate Polarized Partial Charges,' J. Chem. Theory Comput.3, 2011-2033 (2007)
- A.V. Marenich, C.J. Cramer, D.G. Truhlar, 'Generalized Born Solvation Model SM12' J. Chem. Theory Comput.9, 609-620 (2013)
(iso)SS(V)PE solvation calculation
(In Spartan'14 this was called SS(V)PE but has been renamed to distinguish it from the SS(V)PE variants of C-PCM model
The Surface and Simulations of Volume Polarization for Electrostatics (SS(V)PE) method treats the solvent as a continuum dielectric, solving Poisson's equation on the boundary. A dielectric constant is needed for the calculation. For example, POSTSOLVENT=ISOSVP,78.39 would be use for water. References for this method can be found in
- D. M. Chipman, J. Chem. Phys.112, 5558, (2000)
- D. M. Chipman, Theor. Chem. Acc.107, 80, (2002)
- D. M. Chipman, Theor. Chem. Acc.107, 90, (2002)
It should be noted that analytical gradients are not available, so transition state searches with this solvent model should only be applied to small molecules. Another important constraint of our implementation is that only molecules with 'star-like' volumes are allowed. Any ray emanating out from the center can only pass through the surface once.
Our implementation has been designed for small molecules. So for larger molecules one may have to modify internal parameters to get good results. Specifically NPTLEB=, which controls the number of Lebedev points set to 1202. This has been shown to be precise enough for .1 kcal/mol on solutes the size of monosubstituted benzenes. Other possible values are (974,1202,1454,1730,2030,2354,2702,3074,3470,3890,4334,4801,5294).
SM3 solvation method
For legacy purposes Spartan also implements the Cramer-Truhlar SM3 method. The SM54P and SM8 method are much improved over SM3 and should not be used in the future, but can be accessed with the POSTSOLVENT=SM3 keyword.

We use the POSTSOLVENT keyword to do an energy of solvation calculation. This calculation is useful to determine the energy differences among different conformers of the same molecule as the bond lengths and angles do not change significantly when solvent is added.

If one wants to see the effect of solvation on the geometry, (for example for a transition state structure) the ADDSOLVENT= or SOLVENT= should be used. SOLVENT= is a synonym for ADDSOLVENT=. When typed in, it will be erased (following pressing of the Enter/Return key) from the Options line and the 'in-solvent' pull down menu will be updated to reflect the specified solvent.

A longer discussion of how the solvation energy is calculated can be found under solvation methods in the 'Quantum Mechanical Energy FAQs'.

The Cramer-Truhlar methods (SM8, SM54, SM50R, SM3) work only with common organic atoms: H, C, N, O, F, S, Cl, Br, and I. (SM8 adds Si and P if bonded to oxygen.) SM12 covers the entire periodic table. The calculation may proceed with other elements, but important terms of the approximation will be set to zero. If the atoms 'aren't very important' relative solvation energies of conformers might be useful, but absolute values will be poor.

In principle the C-PCM and SS(V)PE methods are not parameterized and are available for any atom of the underlying basis-set, however they do require atomic radii to generate the cavity. By default we use the 'Bondi Radii' increased by 20% to construct the cavity in the PCM solvation calculation. These are vdW radii originally proposed by Bondi, verified by Rowland and Taylor and extended by Cramer and Truhlar.

Bondi, J. Phys. Chem. 68, 441 (1964)
Rowland Taylor, J. Phys. Chem. 100, 7384 (1996)
Mantina et al, J.Phys.Chem. 100, 7384 (2009)

This covers the standard main group atoms: H-Ca, Ga-Kr, Rb,Sr, In-Xe, Cs,Ba, Tl-Rn, Fr,Ra
and a few metals: Ti, Ni, Zn, Ag, Cd, Pt, Au

If alternate atoms are required you may use the PCMRAD= keyword. For example to use a Radii for Iron of 2.2 angstroms one would use PCMRAD=FE~2.2 Note that this is the presumed vdW radii, before being multiplied by the default 1.2 (20%). If there are multiple atoms you can comma separate them. i.e.: PCMRAD=FE~2.2,NI~2.2

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What charge models can be accessed from Spartan?
We have 3 ways of decomposing the quantum mechanics wave function into a set of nuclear charges. These are Mulliken charges, natural charges and electrostatic (ESP) charges.

Mulliken uses a standard Mulliken analysis, taking each two-center term of the density/wave-function, dividing by two and placing 1/2 of the 'electron cloud' on each constituent atom. This approximation is a fair approximation for small, well-balanced basis sets but becomes increasingly poor for larger basis sets.

Natural charges are similar to Mulliken charges, but include more advanced mathematics, such that the results 'behave better' for large basis sets. Natural and Mulliken charges are best used for determining chemical reactivities as a function of charge per atom. (See the discussion on natural bond order for references.)

Electrostatic charge (ESP) is a numerical method that generates charges that reproduce the electrostatic field from the entire wave function. This method is appropriate when the property one is concerned with depends on the mid-to-far electrostatic potential of the molecule/atom. Electrostatic charges may produce poor results for atoms that have little exposed surface area.
In more recent versions of Spartan, the output includes two sets of electrostatic charges. The traditional method calculates a charge for each atom. The newer method places a charge, a dipole, a quadrapole and an octopole on each heavy atom. (We are using these values in internal projects.) The use of atomic dipoles does a better job of modeling the electrostatic potential.
If the printing of charges is turned on ('Charges & Bond Orders' is checked in the Calculations dialogue) 'Q0' represents the atomic charge; 'Qx', 'Qy' and 'Qz' represent the atomic dipole; 'Qxx', 'Qxy', etc. are the components of the traceless quadrapole.

How can I control the parameters of the ESP charge model?

Spartan's ESP charge calculation is based on the 'CHELP' algorithm. In this algorithm the charges at the atom-centers are chosen to best describe the external field surrounding the molecule. Ideally this area should include everything outside of the van der Waals radii. Of course this would be time consuming and may work too hard to get very exact long-range dipole terms at the cost of inaccuracies in the field near the atom. As a compromise, a shell surrounding the atoms is used. The thickness of this shell is 5.5 au. This default value can be modified using the SHELL= keyword in the Options field of the Calculations dialogue. You may also change the inner value of this shell from the VDW to (VDW + WITHIN) with the keyword WITHIN=.

Keyword	Description	Default
SHELL=	The farthest extent of the shell of points to used to fit the electrostatic potential.	5.5 bohrs
WITHIN=	A buffer between the standard vdW radii and the nearest points in the shell of external points.	0.0 bohrs
ELCHARGE=	An integer number representing the number of points per cubic Bohr.	1
CHELPDENSITY=	An integer number representing the number of points per cubic Bohr.	1
SVD=	Use the CHELP-SVD (Single value decomposition) algorithm to calculate the charges. Setting to 0 turns off. There are a number of variants to this algorithm: An older, deprecated, algorithm. Don't prune points. Attempt to prune terms (vectors) which do not significantly improve the accuracy.	0
SVDTHRESH=	.00001
CHELPPOINTS=	Algorithm which places points into the shell. Use a rectangular grid. Use a spherical grid with approximate constant density. Use a spherical grid with density decreasing ~1/radius.	1
CHELPEXTRA=	Choose more points than just nuclei. This allows one to approximate a multipole expansion around each nuclei. Use 1 point per nuclei. Use 7 points per nuclei. Use 10 points per non-hydrogen nuclei. Use 14 points per non-hydrogen nuclei. Use bond orientated, atom centered dipoles Modified version of model 4 adding extra points on atoms with 2 bonds. same as 5, but add dipoles to hydrogens Dipoles on all terminal atoms A flag to cycle through all models By default electrostatic charges are reported using method '0'. However, points using method '2' are also calculated and available to be used.	0

Relevant references:

Chirlian and Francl (J. Comp. Chem. 8 (1987) 894)
Besler, Merz, Kollman (J. Comp. Chem. 11 (1991) 431)

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What is natural bond order?

Natural bond order uses similar mathematics to natural charges but is used to analyze the charge density between atoms, not centered on each atom. See the NBO keyword
Natural Bond Order references:

A. Reed, R. Weinstock and F. Weinhold, 'Natural Population Analysis', J. Chem. Phys. 83, 735 (1985)
J.P. Foster and F. Weinhold, 'Natural Hybrid Orbitals', JACS 102, 7211 (1980)

More information from NBO calculations can be printed with the keyword PROPPRINTLEV=2. This keyword may be useful if you are interested in atomic hybridization of each atom or problems are detected with the NBO calculation.

Spartan's version of natural bond order attempts to find the 'natural' Kekule bonding of each molecule. As such it has issues with delocalized systems. When strong delocalization is detected the calculation will not complete, but one can force the calculation to complete by adding the PROP:IGNORE_WARN keyword (and the PROPRERUN keyword to force the properties module to rerun). In this case the atomic polarization will likely be useful, but the total natural bond order is not to be trusted.

The sum of the square of the coefficients of my MO is not 1. Shouldn't it be normalized?
The MO (molecular orbital) is normalized, and the AO (atomic orbitals) are normalized. But the AOs are not orthogonal. This is why the simple algebraic norm of the coefficients is not 1.0. In order to do any quantitative work with the coefficients of the MO you will need to know the values the AO overlap integral. This is usually referred to as the overlap matrix and is represented as 'S' in the literature.
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How can I print the overlap matrix?

The overlap matrix is the overlap of different atomic orbitals. It can be printed with the PRINTOVERLAP keyword. The ordering of the coefficients is the same as that displayed for the molecular orbitals when the 'Orbitals & Energies' check box is selected in the Calculations dialogue.

What is the spin operator <S²> and what does it say about the wave function?

<S²> is the spin operator, and it is relevant in UHF calculations. While UHF (or ROHF) is required for open shell systems and to get certain bond separation energies correctly, it suffers from the disadvantage that its wave functions are not (exact) eigen-functions of the total spin operator. This is because the UHF ground state can be contaminated with functions corresponding to states of higher spin multiplicity.

<S²> is a measure of spin contamination and is often used as a test of how good the UHF wave function is. Singlet states should have a value of 0.0, doublets 0.75, and triplets 2.0. If <S²> is within +- .02 of these values the wave function is usually considered acceptable.

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M = 1(singlet), 2(doublet), 3(triplet), ...
s = (M-1)/2
<S²> = s*(s+1)
<S²> = 0, 3/4, 2, ...

The <S²> is printed out when the PROPPRINTLEV=1 keyword is used, and is represented in the output file as <S**2>

The default masses are found in the 'MASS.spp' parameter file. ('params.MASS' on Linux machines.) The default value is the mass of the most common isotope. This can be overridden with the AVGMASS keyword, or by changing the isotope of a specific atom in the Atom Properties dialogue.

The strength of RAMAN frequencies are calculated from the change in polarization of the molecule with respect the vibrational mode. As such, this can be much slower than just calculating standard IR intensities (dependent on the change in the dipole). It should be noted that the Intensities shown in the 'Output Summary' and plotted in the RAMAN graphs are scaled by the laser frequency [v_o] (which can be changed in the Options menu -> Preferences -> Settings dialogue), plotted logarithmically and broadened with a Lorentzian.

I(v_i) = S(v_i) * [ (v_o-v_i)⁴ ] / [ v_i*(1-exp^(v_i*C₂)/T) ] Where C₂ is the 'Second radiation Constant'; 1.438777 cm-K.

The units of absorbance is kilometers per mol, km/mol. The justification for this unit can be surprising, so we derive this unit here. The molar absorption coefficient e

e(v) = [1/Cd]log[Io(v)/I(v)] A(v)/Cd

where C is the concentration, (mol/L), d is the path length (cm), Io/I is the intensity ratio (unitless, incident over transmitted) and 'v' is the wavenumber (1/cm). Thus the unit is

[L/(mol*cm)]

However, what is measured is the integrated absorption A

A = ∫A(v)dv ; over the band in question Thus A is in units of [L/(mol*cm)]*[1/cm] [1000cm³/mol*cm²] = 10m/mol. Multiplying by a hundred gives the units most often used in experiment and in Spartan: 1000m/mol = km/mol.
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How can I use the intrinsic reaction coordinate (IRC) procedure?

Spartan can generate a reaction path using three approaches. The simplest is via the 'energy profile' calculation, which changes specific coordinates. (See the discussion of energy profile.) This works well for simple systems when the reaction coordinate can be well represented as internal coordinates (such as bond distance).

A reaction path can also be generated by the calculation of the Transition State Geometry along with a frequency calculation. A list file can be generated for the single imaginary frequency corresponding to the reaction coordinate.

Spartan has also implemented a reaction coordinate algorithm to generate a reaction path given a transition state using the algorithm by Schmidt. (M.W. Schmidt, M.S. Gordon, M. Dupuis, J. Am. Chem. Soc. (1985), 107, 2585) This can be specified by selecting the IRC checkbox when performing a transition state geometry calculation. When selected, a new file will be generated that contains the reaction path. The IR check box should also be selected. If you know you have a good transition point and a good Hessian the IRC can be run as a single point 'Energy' calculation with the BE:IRC keyword.

The IRC calculations are time consuming. It is suggested that users confirm that a 'good transition state' has been found before resubmitting the with the IRC algorithm enabled. Confirm both, that the gradient is small and that there is only 1 negative eigenvalue.

Keywords related specifically to IRC calculation can be found in the keyword section.

Spartan offers a number of ways to work with excited states, of varying complexity and cost. However, since nearly all ground states are singlets, and the first excited state is almost always the lowest triplet the easiest thing to do is look at the 'Ground State' with two unpaired electrons. This is almost always 'accurate enough' and much faster than any of the more advanced methods.

As an example I'll look at benzene. I first optimized structure for benzene in its ground state. (The HOMO-LUMO gap of 6.6 ev for this singlet would be a first approximation of the excited state energy.) I next Copy+Pasted that in the spreadsheet and redid the calculation as a triplet. I did this twice; once with a triplet optimization, and once at the same Singlet Geometry. The energy gain from going from singlet to triplet is shown in the 'Rel. E (eV)' column (Notice equation highlighted) The Single point energy would be the appropriate number for fluorescence (vertical excitation) , and the triplet optimization would be for phosphorescence.

Notice that for the triplet opt, I turned off symmetry with the IGNORESYMMETRY keyword and checked the IR checkbox (which becomes the FREQ keyword) to ensure that I've found the real triplet minimum. (Any negative frequencies would indicate that symmetry was not broken enough.)

As an example of a different approach/theory notice that I checked UV/Vis check-box on the ground-state singlet. (The UVVIS keyword.) [I added KEEPVERBOSE, INCLUDETRIPLETS as mentioned in our help. I also added UVSTATES=4 because benzene is a difficult casebad convergence] If you examine the verbose output for this you will see that using full TDDFT theory, the excited state energy (vertical excitation) is 3.88 ev. (The TDA approximation gives 4.24 ev.)

...TDDFT is probably better ..... needed for other excited states or singlet->singlet transitions.

We can do optimizations at the TDDFT level, as is shown in the final row. This can be very slow, (prohibitively slow for DFT functionals where we do not have analytical gradients such as EDF2).

The UV/Vis spectra is calculated by running a single point CIS calculation (or TD-DFT calculation for DFT methods) after the main wave function has been calculated. In CIS theory, the absorption energies are the difference between the HF ground state and CIS excited state energies. A reference for Spartan's CIS implementation:

J.B. Foresman, M. Head-Gordon, J.A. Pople, M.J. Frisch, J. Phys. Chem. (1992), 96, 135.

For DFT calculations, excited states are obtained using the time-dependent density functional theory (TD-DFT) approach to generate excited states from excitations of the ground state molecular orbitals. The Tamm-Dancoff approximation (TDA) is also available to speed up the calculations:

E. Runge, U. Gross, Phys. Rev. Lett. (1984) 961533] A CIS-like Tamm-Dancoff approximation [S. Hirata, M. Head-Gordon, Chem. Phys. Lett. (1999) 302 375S.

Hirata, M. Head-Gordon, Chem. Phys. Lett. (1999) 314 291

This calculation is similar to the CIS calculation, and most keywords controlling the excited state CIS calculation are used in the TDDFT calculation.

A UV/Vis calculation is done, by default, whenever a single-point excited state calculation is specified. If one needs to modify the UV/Vis calculation, (other than with the UVSTATES keyword) a single point excited state calculation must be performed, using the keywords described below.

See the keyword section on CIS/TDDFT for relevant keywords. If you want a geometry optimization for something other than the first excited state, use the ESTATE=n keyword to choose a different excited state. (Note that when you hit the 'Enter' key the ESTATE keyword disappears and the n appears where the 'First Excited' in the first line of the calculations dialogue.

Often you may want the first excited singlet state, which may or may not be the actual first excited state. To limit the search of possible excited states to singlets you can type in the keyword CIS_TRIPLETS=FALSE.

Assuming that the real ground state is a singlet, and the first excited state is not a triplet, these both refer to the same electronic state. A difference exists in how Spartan calculates these; excited state calculations use either CIS or TDFT methods while ground state calculations use HF or DFT methods. The later may not be as accurate, but are much faster, especially in the context of geometry optimizations.

It is also possible that the first excited state is another singlet, and not a triplet. If in doubt you can do an energy calculations with the 'UV/Vis Spectrum' and the INCLUDETRIPLETS keyword to examine all the excited states. Note that the description of singlet/triplet is found in the verbose output so you will need to add the KEEPVBOSE keyword. Graphically, the intensity of the singlet to triplet will be very small.

It should be noted that information on each excitation can be found in the verbose output. The notation:

D(10)->V(2) refers to the excitation of an electron from the 10-th doubly occupied MO to the 2nd virtual MO. Often, an excitation will take contributions from multiple molecular orbitals.

The Transition dipole moment and oscillator strength are also printed. The oscillator strengths are used by Spartan to graphically display the UV/Vis spectrum. To convert the oscillator strength to absorbance, we divide by 4.319x10^-7. Usually the log (base 10) of the absorbance is used to display the spectrum.

By default only pairs of filled/unfilled orbitals which have amplitudes larger than 0.15. To see more components you can use the CIS_AMPL_PRINT=1 keyword to see (nearly) all of the components. The sum of the square of all components will add to 1.0.

Spartan's NMR package is based on the Kussman Ochsenfeld linear scaling algorithm using 'gauge-including' atomic orbitals:

C. Ochsenfeld, J. Kussmann, F. Koziol, Angew. Chem., 116, 4585, (2004).
F. London, J. Phys. Radium, 8, 397, (1937)
K. Wolinski, J. F. Hinton, P. Pulay, J. Am. Chem. Soc., 112, 8251, (1990).

This scheme has been proven to be reliable and accurate for many applications, see

T. Helgaker, M. Jaszunski and K. Ruud, Chem. Rev., 99, 293, (1990).
C. Ochsenfeld and M. Head{Gordon, Chem. Phys. Lett., 270, 399, (1997).
S. P. Brown, T. Schaller, U. P. Seelbach, F. Koziol, C. Ochsenfeld, F.-G. Klarner, H. W. Spiess, Angew. Chem. Int. Ed., 40, 717, (2001).
C. Ochsenfeld, F. Koziol, S. P. Brown, T. Schaller, U. P. Seelbach, F.-G. Klarner, Solid StateNucl. Magn. Reson., 22, 128, (2002).
C. Ochsenfeld, J. Kussmann, F. Koziol, Angew. Chem., 116, 4585, (2004).

Chemical shifts are given in parts-per-million (ppm) relative to the appropriate standard (nitromethane for nitrogen, fluorotrichloromethane for fluorine, and TMS for hydrogen, carbon and silicon). These relative shifts are available for most common DFT functionals and basis sets. One can edit the 'NMR_References.spp' file found in the Spartan shipping directory to add new standards.

Spartan can also apply systematic corrections to the Carbon NMR depending on the nearby chemical environment. These are referred to as 'corrected shifts' in Spartan.

We use modified Karplus equations to predict hydrogen coupling constants.

'Vuister and Bax', 1993a and 'Wang and Bax 1996' for amide bonds.
'Haasnoot, de Leeuw and Altona (1980)' for sp3-sp3 3JHH linkages
When 2JHH couplings are calculated, we have a few empirical values from table 4.6 (pg. 151) 'Organic Structure Analysis 2nd ed.' P.Crews, J.Rodriguez, M.Jaspers.

The NMR calculation has its own set of SCF convergence issues. Usually the default parameters are good enough to get reasonable answers, but at times you may need to change these to get difficult systems to converge. The first thing to do is to make sure the integrals are more accurate than usual by typing the CONVERGE keyword in the Options line of the Calculations dialogue.

If you continue to have difficulty you will have to adjust some of the internal parameters to the multi-step SCF logic. The most common problem is errors with 'level-2' iterations. By default this fails after 75 steps. This can be increased with the D_SCF_MAX_2= keyword. A list of other NMR related keywords can be found in the keyword table below.

What is the score used to rank alignments?

The score used for alignment is designed to be 1 for a perfect fit and 0 for a terrible fit. For a system with N centers:

score = 1 - U/NU = sum[i=1,N; G_i(r_i-ro_i)]

'r_i' is the i'th center of the trial molecule, and 'ro_i' is the corresponding center of the template molecule. G is a function which behaves like the usual Hookean spring for small values. (~(r_i-ro_i)²) but approaches 1 as the difference in distances (r_i-ro_i) goes to infinity

G = (1/3)*[ (r_i-ro_i)/R_i]²G = (1/3)*{3 - 3[(r_i-ro_i)/R_i]^-2 + [(r_i-ro_i)/R_i]^-4 }

The second equation is used when (r_i-ro_i)/R_i is greater than 1.0. The normalizing R_i is (3/5) of the van-der-Wall radii for atoms, and for CFD's is the radii given in the property panel when a CFD is selected.

The distinguishing feature of this function when compared to a simple RMSD type function ((r_i-ro_i)² is that in the case where most of the centers will line up exactly, but only 1 is nowhere near matching, the latter center will adversely affect the alignment of the former centers. As an example, let's try to map the H2 molecule onto a template of the Br2 molecule with R_Cl set anomalously small, say 1/10 of an angstrom. The 'best' (and only) minima found by the RMSD function is the H2 molecule centered symmetrically at the center of the Br2 molecule. The score we use would find an off-center minima with one hydrogen directly on one Bromine, and the other Hydrogen near the center of the Br2 molecule.

When aligning two separate sets of centers, a number of alignments are examined. It should be noted that the 6-dimensional translation/rotation space of the above function can have many local minima, or alignments. These are minimized and examined, and the best one is returned. Also, a second score is used internally: 'the number of 'matched centers'. This score closely matches the reported score, but any alignment in which some center-pairings do not line up with R_i are rejected, prior to comparing actual score values.

What is the score used to rank molecules in the similarity module

The score used in alignment is used in the similarity task. The similarity task is more time consuming than alignment in that similarity will look at multiple ways of matching two molecules using different atom mappings and/or pharmacophores, and can look at multiple conformations stored in 'Similarity Libraries'. This score can be displayed in the resulting spreadsheet by typing

SimilarityScore=@SCORE() into a column header of the spreadsheet.
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Geometries
Cartesian coordinates are typically given in Ångstroms (Å), but are also available in nanometers (nm) and atomic units (au).
Bond distances are typically given in Å, but are also available in nm and au. Bond angles and dihedral angles are given in degrees (°).
Surface areas are typically given in Å ² and volumes inÅ³, but are also available in nm² (nm³) and au² (au³).
1 Å = 0.1 nm = 1.889762 au
Energies, Heats of Formation and Strain Energies
Total energies from Hartree-Fock, density functional and MP2 calculations are typically given in au, but are also available in kcal/mol, kJ/mol and electron volts (eV).
Heats of formation from semi-empirical calculations are typically given in kJ/mol, but are also available in au, kcal/mol and eV.
Strain energies from molecular mechanics calculations are typically given in kJ/mol, but are also available in au, kcal/mol and eV.
Orbital Energies
Orbital energies from Hartree-Fock, density functional and MP2 calculations are typically given in au, but are also available in kcal/mol, kJ/mol and eV.
Orbital energies from semi-empirical calculations are typically given in eV, but are also available in kcal/mol, kJ/mol and au.
Energy Conversions
Energy Conversions^a
au kcal/mol kJ/mol eV
1 au - 6.275x10² 2.625x10³ 2.721x10¹
1 kcal/mol 1.593x10^-3 - 4.184 4.337x10^-2
1 kJ/mol 3.809x10^-4 2.390x10^-1 - 1.036x10^-2
1 eV 3.675x10^-2 2.306x10¹ 96.485 -
Graphical Properties
Electron densities and spin densities are given in electrons/au³.
Dipole moments are given in debyes.
Electrostatic potentials are given in kcal/mol.
Other Properties
Atomic charges are given in electrons.
Vibrational frequencies are given in wavenumbers (cm^-1).

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Below are some commonly used conversion factors: *In places where multiple values are listed for a given conversion, the first is the approximation used in Spartan, the second is the 'exact' value (as of 1973, 1986 or 1998).
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Below are some important constants used in quantum chemistry: *In places where multiple values are listed for a given conversion the first is the approximation used in Spartan, the second is the 'exact' value (as of 1973, 1986 or 1998).
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No. Data sets using the older constants have been generated for more than 25 years. To make sure newer versions maintain backward compatibility we continue to use the older values for these fundamental constants and conversion factors. Even though each new digit is an important scientific achievement, the increased precision is well beneath the noise present in the chemical measurements Spartan deals with.
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Keywords

Below is a list of all keywords which the property module understands. Keywords specific to the property module


KEEPVERBOSE	By default the verbose output file is deleted/pruned. (For many jobs this can dramatically decrease the size of .spartan files.) Instead of using this keywords, one can set the 'Keep Verbose' check box in the 'Preferences Panel'.
PROPPRINT=i PROPPRINTLEV=i	For 'i' greater than 1, print more information into the output file. 'i' must be 4 or less.	0
PRINTCOORDS	Print the Cartesian coordinates of all atoms in the system.
ACCEPT	Accept certain error conditions and continue without a fatal error.
BTABLE=BAD	Print out a table on all bond distances (B), bond angles (A) and dihedral (D) angles. If only bond distances, angles or dihedrals are required, BAD can be replaced with B, A, or D respectively.
NEAREST=x.y	Specify the multiplication factor (applied to nearest-neighbor distances) when generating the geometric information.	1.2
QSAR	Prints various QSAR descriptors. While these values are usually calculated, and can be found in the proparc file and in the spreadsheet this prints them to the output file. The list of descriptors this keyword prints is: Atomic Weight E-LUMO and E-HOMO Electronegativity, Hardness and Est. Polariz. (AM1 only) Molecular Volume, Surface Area and Ovality logP (Ghose-Crippen, Dixon, and Villar[SE only]) Exposed Surface Area Atomic Valence Q-minus and Q-plus (for any charges) Free Valence Total Overlap Population (ab initio only)
NOQSAR	Skip the calculation of QSAR descriptors.
MOMENTS	Print out the moments of inertia, in both atomic units and inverse centimeters.
MAXVOLSIZE=i	Atomic volumes and surface areas will be calculated only for systems with fewer than 'i' atoms.	100
SOLVRAD	In calculation of atomic areas and volumes, add this value to the VdW radii.
VPTS=i AARCS=j APTS=k	To control the internal working of the volume calculator.
POSTSOLVENT=xxx² ADDSOLVENT=yyy² SOLVENT=zzz^1,2	To select different solvation models. See the discussion on solvent methods and the SOLVENT= keyword.
TESTPROPS=1	Internal keyword used for debugging and QA work at Wavefunction. This works on the 'cell' data of the spreadsheet. Cells with the following names are analyzed: Reference_E=xxx.yy ; The energy in Kcal/mol. REF_PREC_E=x.yyy ; precision (default 5.0e-8) PROP_x=Equation ; Most spreadsheet equations are valid REF_PROP_x=xxx.yy ; the target value REF_PREC_x=x.yyy ; precision (default 1.0e-4)
PARCFORMAT=i	[for internal to Wavefunction use] If i=1 write both formats of frequency information. If i=2 write only new format of frequency information.	i=2
Keywords to the analyze wave function
PRINTMO¹	Print the Molecular orbitals.
PRINTORBE ORBE	Print molecular orbital energies.
PRUNEVIRTUAL=x PRUNEVIRTUAL=NONE	Delete unoccupied molecular orbitals 'x' above the LUMO. This is useful in decreasing the size of the molecular data stored on the disk and in making the output of PRINTORBE and PRINTMO more reasonable.	10
POSTHF	Use the post Hartree-Fock wave function if available. On by default for MP2 type calculations.
NOPOSTHF	Do not use the post HF calculations. For MP2 this means, to use the HF wave function instead of the corrected MP2 wave function,
IGNOREWVFN	Skip all wave function dependent properties.
NBO NBO=yy	Do the natural bond order hybridization analysis. See the above discussion. Possible values for yy are: NORMAL, the default. IONIC to see ionic contributions. 3C to examine three-center contributions.
MULPOP¹ PROP:MULPOP=3	Print the Mulliken charges. With a value of 3, the full matrix is printed,	1
NOMULCHARGE NOMULPOP	Skip the Mulliken charge calculation.
POP¹	Print the natural atomic charges.
NONATCHARGE	Skip the natural atomic charge calculation
PRINTCHG PRINTCHARGE=x	Print a summary of charges and bond order. A (much) shortened version of what is printed with the MULPOP, POP, BONDORDER and NBO keywords. If x=1 only atomic charges are printed. If x=2 Mulliken bond orders are shown. If x=2 natural bond orders are shown.
DEORTHOG	Deorthogonalize semi-empirical MOs before calculating properties.
DIPOLE	Print out the Cartesian components of the dipole moment.
NODIPOLE	Skip the calculation of the dipole moment.
BONDORDER	Print out Mulliken and Lowdin bond order matrices, plus atomic and free valences for open-shell wave functions.
PRINTNBO	Print the AO to NBO transformation
NOPOP	Skip the natural bond order (NBO), and natural charge calculation.
DOEPN	Print out the 'Electronic Potential at Nuclei' for Oxygen and Nitrogen. DOEPN=SKIP to skip calculation. (By default the calculation is stored in archive but not printed. Enter DOEPN=ALL to print all atoms.
PRINTS	Print the atomic orbital overlap matrix (S).
LOGP=	See the discussion on the logP calculation
ELP	Specify that the elpot+polpot grid will be used to generate atomic charges. This is valid for closed-shell HF-only molecules.
PRINTOVERLAP PRINTS	Print the overlap matrix as a lower triangle. Use in conjunction with the 'Print: Orbitals & Energies' check box if you want to do your own 'home-brew' quantum mechanics calculation. See the discussion of atomic orbitals for more information. (The PRINTS spelling is deprecated.)
POLAR	Calculate the static polarizability of the molecule. For Hartree-Fock and semi-empirical methods this will also calculate the static hyperpolarizability. See our discussion above for more details on how to calculate polarizability.
HYPERPOLAR	Calculate the static polarizability and hyperpolarizability of the molecule. Not available for DFT methods using pure basis sets (i.e. 6-311G etc.).
POLAR=a,b,c...UNIT HYPERPOLAR=a,b,c...nnUNIT	Calculate the polarizability at different frequencies. There can be multiple frequencies, here represented by 'a','b', and 'c', but could be more (or fewer) comma separated values. UNIT should be replaced with au, nm, ev, hz or cmInv. For example: POLAR=0.0,0.03,0.05,AU Note that an energy of 'zero' (0.0) is a way of specifing the static (infinite wavelength) case.
POLAR=WALK,start,end,step,UNIT	This format of the POLAR keyword allows one to specify a range of frequencies/energies. This WALK format is also available for the HYPERPOLAR keyword. As an example: POLAR=WALK=0,.1,0.025,AU
EMFIELD=	Can apply an external (multipole) field to the main calculation. Thus allowing a numerical way of calculating static polarizability. One stipulate multiple comma separated Cartesian terms representing dipoles (X,Y,Z), quadrapoles (XX,XY,YY etc.). For example: EMFIELD=X~0.1 EMFIELD=X~0.1,Y~0.05,ZZ~0.001 The units are in 'atomic units'. ie. 1 a.u. = 51.422 V/Å
Keywords related to frequencies and thermodynamics
NOFREQ	Do not do any frequency or thermodynamic calculation even if there is a good Hessian. (By default, if a high quality Hessian is available, frequencies will be calculated.
FREQSCALE=x FSCALE=x	Scale all the frequencies by a factor 'x'.
DROPVIBS=x	When calculating thermodynamics values, ignore all modes with frequencies below 'x'.
CLAMPTHERMO CLAMPTHERMO=x	When calculating thermodynamics values, clamp enthalpy terms at 'x'RT. (If no 'x' given 1/2 is used.) Entropy and the heat capacity will be clamped at 'x'R. For 'x'=1/2 these limits imply a break in the enthalpy, entropy and heat capacity at ~260 cm^-1, ~116 cm^-1 and ~2 cm^-1 respectively. To turn 'clamping' off use CLAMPTHERMO=NO	0.5
PRINTMODE	Print thermodynamic information for each mode.
TEMPERATURE=	Change the default temperature used in the thermodynamic calculation.	298.15 K
TEMPRANGE=start,end,step	Print thermodynamic properties for a range of temperatures.
PRESSURE=	Change the default pressure used in the thermodynamic calculation.	1.0 atm
PRINTFREQ¹	Print the Cartesian values of the normal mode vibrations. This is what the 'Print Vibrational Modes' button in the calculation dialogue.
THERMO¹	Print standard thermodynamic data. This is the 'Print Thermodynamics' button in the calculation dialogue.
PRINTIR	Print Infrared and thermodynamic information for each normal mode vibration.
PRINVIBCOORDS	Print the coordinates of each vibrational mode.
AVGMASS ISOTOPEMASS=*	By default Spartan uses the terrestrial average mass of atoms when doing thermodynamics calculations. (Changing the isotope of a specific atom in the property dialogue overrides the mass for only that atom.) DEFAULT: the default use average mass. COMMON: use the most common isotope as the default atomic mass. (This was the default in previous versions of Spartan.) STANDARD: use the average mass, and ignore any specific atomic mass settings set in the atom property panel.
APPROXFREQ	Calculate frequency and thermodynamic information on the intermediate low quality Hessian. (Not recommended.)
GXTHERMO	Calculate G3 type results. (Internal keyword, should not be used unless you know what you are doing.)
FREQ^1,2 FREQ=CD² FREQ=FD²	Calculate frequencies by numerical differentiation, using central differences (CD) or forward differences (FD) as opposed to analytically. Analytical methods are usually much faster and more accurate than numerical methods as numerical methods require 6 single point calculations for each atom in the molecule. Forward difference is usually %50 faster than central differences, but is significantly less accurate and is not recommended. The default is to use analytical frequencies if available.
NUMERICALFREQ	Calculate frequencies by numerical differentiation, using central differences. Analytical methods are usually much faster and more accurate than numerical methods as numerical methods requires 6 single point calculations for each atom in the molecule.
FD=xx.yy²	Step size for numerical differentiation.	0.005 bohr
DORAMAN²	Calculate the Raman intensities along with the standard IR intensities.
Keywords related to electrostatic (ESP) charges See How can I control the parameters of the ESP model? for more details and some additional keywords.
ELCHARGE¹	Print information about the electrostatic charges.
NOELCHARGE	Skip the electrostatic charge calculation.
CHELPPRINT=i	Print more information about the ESP charge calculation. Integers greater than 1 cause successively more printing. Also available is TERSE	1
Keywords related to the Intrinsic Reaction Coordinate (IRC) calculation See How can I use the Intrinsic Reaction Coordinate procedure? for more details
IrcSteps=²	Specifies the maximum number of points to find on the reaction path. (Should be odd. The default value of 41 yields 20 steps forward and 20 backwards.)	41
IrcStepSize=²	Specifies the maximum step size to be taken. This is in thousandths of a Bohr. The default of 150 means 0.15 Bohr.	150
RPATH_TOL_DISPLACEMENT=²	Specifies the convergence threshold for the step. If the atoms are moving less than this value, configuration is assumed to be at a minima and the algorithm will stop. The units are in millionths of a Bohr. The default value of 5000 corresponds to 0.005 Bohr.	5000
Keywords related to the excited state and UV/vis calculation see Controlling an excited state calculation
ESTATE=n^1,2	Choose the excited state to calculate the gradient for. Usually this is not entered as a keyword, but is selected by choosing 'First Excited State' in the calculation dialogue.	1
TDA	Use the Tamm-Dancoff approximation (TDA) to then standard Time Dependent DFT (TDDFT) algorithm. (The TDA was the default method for DFT calculations prior to Spartan'14v117.) This can be up to twice as fast as the default 'Full TDDFT' and produces similar, but not as precise results.
CIS_N_ROOTS=²	To examine more orbitals in the excitation. For systems where there are many delocalized atoms you may want to increase this number from the default. Despite the 'CIS' in this keywords spelling, it is also appropriate for TDDFT calculations.	>=5
CIS_TRIPLETS=FALSE²	To limit the search of excited states to only singlets. Use this keyword only for excited state calculations. If this is used when doing an UV/Vis spectrum calculations this keyword will interfere with the INCLUDESINGLETS and INCLUDETRIPLETS keywords.	=TRUE
UVSTATES=²	To examine more orbitals in the UV/Vis calculations. For systems where there are many delocalized atoms you may want to increase this number from the default. Only valid when the 'UV/Vis' button is selected.	>=5
INCLUDETRIPLETS²	To include triplets in the UV/Vis calculation of singlet wave functions. The intensity of the excitation will be small (zero) but can be useful if interested in all lower energy excited states.
INCLUDESINGLETS²	To include singlet excitations in the UV/Vis calculation of triplet wave functions. The intensity of the excitation will be small (zero) but can be useful if interested in all lower energy excited states.
CORE=FROZEN²	By neglecting core electrons the calculation can be speeded up.
N_FROZEN_VIRTUAL=n²	Reduces the number of virtual molecular orbitals used in the calculation. Changing this number from the default, may speed up the calculation, but may also cause inaccuracies in the calculation.
MAX_CIS_CYCLES=n²	To change the number of SCF cycles to try before 'giving up' on the CIS calculation. Increase if you are having convergence problems, but waiting longer might work.	10
CIS_CONVERGENCE=x²	Decrease this number if you want quicker convergence at the cost of precision. (Reducing to a number below 5 can give unphysical results.)	6
CIS_AMPL_PRINT=x	To print filled/unfilled molecular orbital pairs which have coefficients larger than x. This value is in hundredths so the default value of 15 implies an amplitude of 0.15. (This will go in the verbose output file, so make sure to use the KEEPVERBOSE keyword.)	15
Keywords related to the NMR calculations see Difficulty with NMR calculation
D_SCF_MAX_2=n	The maximum number of SCF-NMR steps to try before giving up. Typically, increasing this will allow difficult systems to converge.	75
D_SCF_CONV_2=n	The tolerance/precision used in the inner (2^nd) part of the convergence algorithm. 'n' is the decimal so the default of 2 implies 10^-2=0.01.	2
D_SCF_MAX_1=n	Maximum number of tries in the inner NMR convergence step.	40
D_SCF_CONV_1=n	The tolerance of the inner NMR convergence step.	0
Notes: ¹ Indicates that these should not be typed in as there is a button in the calculation dialogue for it. ² The keyword is used by a module other than the property module, but is mentioned here for completeness.

Last modified: Wed Jun 6 15:10:39 GMT 2018

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It is a software that allows you to create your wave tables free of cost. Serum Vst Torrent is an advanced version of this software which is especially designed to create wave tables. It also gives you attractive graphical user interface with full of the professional tools. Each one of the tool has equipped with its wonderful features that you love to apply. It also provides you four different sounds sources to use according to your project. It also has two independent wave oscillator, sub-oscillator and deluxe noise generator.

This serum crack also allows you to edit or adjust your wave table by change frequency and additive sound chart in producing process. This software is equipped with a mathematical formula with a predefined set of useful functions. It helps you to create your own unique wave table settings and provide you to import audio directly from the audio files and much more. It is basically a wave table synthesizer with a high quality of sound, a visual and the creatively oriented interface.

Key Features

It provide a built-in feature to make your own effects.
You can easily import the audio.
Custom wave tables are easily created.
It user interface is very simple.
User-friendly.
It give you a high quality of sounds.
It has supported advanced visual and creative tools.
Easy and professional way to create sounds.
Create the audio artifacts.
It has the advances LFO controlling.
By a single oscillator you can use 16 voices at once.

How to Install

Download the serum software.
Extract the files.
After extracting the file click on installation.
After installation close the software.
Copy and paste the crack.
Now enjoy yourself.

Pros

Its interface is very simple workflow oriented.
It has many qualities of effects and the filters.
Creates a clean and clear sound.
It has Ultra-clean oscillators.

Cons

It main disadvantage is that it sometimes uses multiple processors.

System Requirements

OS: Windows 7/8/8.1/10
Intel 64-bit processor
Hard Disk: 1 GB
RAM: 8 GB
Display Resolution: 1024 x 768

License Keys

SIHC-YDFX-DPKY-GZKD-VQDX

SEFE-JSVD-EJJG-MHCS-URMQ

One of the tip to identify that the site is genuine or spams is that user has to check out the URL of that specific site. The secure sites contain on their start. Windows 7 ultimate 64 bit keygen. Other sites may have the virus, malware, and other malicious files.

SYJF-YITA-CXUN-MIGX-MOHX

Drummadic Vst Cracked Software

Download Links

Drummadic Vst Cracked Windows

Conclusion

Drummadic Vst Cracked Torrent

Serum crack is used to create your own wave table in a variety of ways. By using this software you can easily import the audio files. You can easily and in efficient manner adjust or edit your wave table by changing the frequency. So in this way you can create your own unique wave table. It also give you a high quality and clean and clear sound.

electronegativity	= -(HOMO + LUMO)/2
hardness	= -(HOMO - LUMO)/2

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