An algorithm for variational calculations of molecules with one π electron performed with all-electron explicitly correlated Gaussian (ECG) functions with floating centers is derived and implemented. The algorithm includes the analytic gradient of the Born-Oppenheimer electronic energy determined with respect to the ECG exponential parameters and the coordinates of the Gaussian centers. The availability of the gradient greatly accelerates the variational energy minimization. The algorithm is tested in calculations of four electronic excited states, c3Πu, C1Π u, i3Πg, and I1Πg, of the hydrogen molecule at a single internuclear distance specific to each state. With the use of the analytical energy gradient, the present calculations yield new, lowest-to-date, variational energy upper bounds for all four states.
All Science Journal Classification (ASJC) codes
- Physics and Astronomy(all)
- Physical and Theoretical Chemistry