This method keyword requests an excited state calculation using the time-dependent Hartree-Fock or DFT method [Bauernschmitt96a, Casida98, Stratmann98, VanCaillie99, VanCaillie00, Furche02, Scalmani06]; analytic gradients are available in Gaussian 09 [Furche02, Scalmani06].
Note that the normalization criteria used is <X+Y|X-Y>=1.
Electronic circular dichroism (ECD) analysis is also performed during these calculations [Helgaker91, Bak93, Bak95, Olsen95, Hansen99, Autschbach02]
Singlets
Solve only for singlet excited states. Only effective for closed-shell systems, for which it is the default.
Triplets
Solve only for triplet excited states. Only effective for closed-shell systems.
50-50
Solve for half triplet and half singlet states. Only effective for closed-shell systems.
Root=N
Specifies the “state of interest”. The default is the first excited state (N=1).
NStates=M
Solve for M states (the default is 3). If 50-50 is requested, NStates gives the number of each type of state for which to solve (i.e., the default is 3 singlets and 3 triplets).
Add=N
Read converged states off the checkpoint file and solve for an additional N states. This option implies Read as well.
Read
Reads initial guesses for the states off the checkpoint file. Note that, unlike for SCF, an initial guess for one basis set cannot be used for a different one.
EqSolv
Whether to perform equilibrium or non-equilibrium PCM solvation. NonEqSolv is the default except for excited state optimizations and when the excited state density is requested (e.g., with Density=Current or All).
IVOGuess
Force use of IVO guess. This is the default for TD Hartree-Fock. NoIVOGuess forces the use of canonical single excitations for guess, and it is the default for TD-DFT. The HFIVOGuess option forces the use of Hartree-Fock IVOs for the guess, even for TD-DFT.
SOS
Do sum-over states polarizabilities, etc. By default, all excited states are solved for. A list of frequencies at which to do the sums is read in. Zero frequency is always done and need not be in the list.
Conver=N
Sets the convergence calculations to 10-N on the energy and 10-(N-2) on the wavefunction. The default is N=4 for single points and N=6 for gradients.
Energies and gradients using Hartree-Fock or a DFT method.
CIS, ZIndo, Output
Here is the key part of the output from a TD excited states calculation:
Excitation energies and oscillator strengths:
Excited State 1: Singlet-A2 4.0147 eV 308.83 nm f=0.0000 <S**2>=0.000
8 -> 9 0.70701
This state for optimization and/or second-order correction.
Copying the excited state density for this state as the 1-particle RhoCI density.
Excited State 2: Singlet-B1 9.1612 eV 135.34 nm f=0.0017 <S**2>=0.000
6 -> 9 0.70617
Excited State 3: Singlet-B2 9.5662 eV 129.61 nm f=0.1563 <S**2>=0.000
8 -> 10 0.70616
The results on each state are summarized, including the spin and spatial symmetry, the excitation energy, the oscillator strength, the S2, and (on the second line for each state) the largest coefficients in the CI expansion.
The ECD results appear slightly earlier in the output as follows:
1/2[<0|r|b>*<b|rxdel|0> + (<0|rxdel|b>*<b|r|0>)*]
Rotatory Strengths (R) in cgs (10**-40 erg-esu-cm/Gauss)
state XX YY ZZ R(length) R(au)
1 0.0000 0.0000 0.0000 0.0000 0.0000
2 0.0000 0.0000 0.0000 0.0000 0.0000
3 0.0000 0.0000 0.0000 0.0000 0.0000
1/2[<0|del|b>*<b|r|0> + (<0|r|b>*<b|del|0>)*] (Au)
state X Y Z Dip. S. Osc.(frdel)
1 0.0000 0.0000 0.0000 0.0000 0.0000
2 -0.0050 0.0000 0.0000 0.0050 0.0033
3 0.0000 -0.2099 0.0000 0.2099 0.1399
Last updated on: 9 Jun 2009