Q-Chem 4.3 User’s Manual

# 9.7 Hessian-Free Transition State Search

Once a guess structure to the transition state is obtained, standard eigenvector-following methods such as the Partitioned-Rational Function Optimization (P-RFO)  can be employed to refine the guess to the exact transition state. The reliability of P-RFO depends on the quality of the Hessian input, which enables the method to distinguish between the reaction coordinate (characterized by a negative eigenvalue) and the remaining degrees of freedom. In routine calculations therefore, an exact Hessian is determined via frequency calculation prior to the P-RFO search. Since the cost of evaluating an exact Hessian typically scales one power of system size higher than the energy or the gradient, this step becomes impractical for systems containing large number of atoms.

The exact Hessian calculation can be avoided by constructing an approximate Hessian based on the output of FSM. The tangent direction at the transition state guess on the FSM string is a good approximation to the Hessian eigenvector corresponding to the reaction coordinate. The tangent is therefore used to calculate the correct eigenvalue and corresponding eigenvector by variationally minimizing the Rayleigh-Ritz ratio . The reaction coordinate information is then incorporated into a guess matrix which, in turn, is obtained by transforming a diagonal matrix in delocalized internal coordinates   to Cartesian coordinates. The resulting approximate Hessian, by design, has a single negative eigenvalue corresponding to the reaction coordinate. This matrix is then used in place of the exact Hessian as input to the P-RFO method.

An example of this one-shot, Hessian-free approach that combines the FSM and P-RFO methods in order to determine the exact transition state from reactant and product structures is shown below:

Example 9.199

```\$molecule
0  1
Si   1.028032  -0.131573  -0.779689
H    0.923921  -1.301934   0.201724
H    1.294874   0.900609   0.318888
H   -1.713989   0.300876  -0.226231
H   -1.532839   0.232021   0.485307
****
Si   0.000228  -0.000484  -0.000023
H    0.644754  -1.336958  -0.064865
H    1.047648   1.052717   0.062991
H   -0.837028   0.205648  -1.211126
H   -0.8556026   0.079077   1.213023
\$end

\$rem
jobtype         fsm
fsm_nnode   18
fsm_mode     2
fsm_opt_mode 2
method      b3lyp
basis       6-31g
symmetry false
sym_ignore true
\$end

@@@

\$rem
jobtype ts
max_scf_cycles 250
geom_opt_dmax 50
geom_opt_max_cycles 100
method b3lyp
basis 6-31g
symmetry false
sym_ignore true
\$end

\$molecule