Dynamic Correlation on the Adaptive Sampling Configuration Interaction (ASCI) Reference Function: ASCI-DSRG-MRPT2.

A balanced description of static and dynamic electron correlations is at the heart of quantum chemical methods. To obtain accurate results in strongly correlated systems using wave-function-based methods, a large active space is necessary to ensure correct descriptions of static correlations. Correcting the results for dynamic correlations is also necessary. In this work, we present implementations of second-order perturbation theory for dynamic correlations based on the adaptive sampling configuration interaction self-consistent field (ASCI-SCF) method. In particular, we implemented spin-free driven similarity renormalization group second-order multireference perturbation theory (DSRG-MRPT2). The extrapolation of the ASCI + PT2 energy based on the relaxed Hamiltonian in DSRG-MRPT2 gives a reasonable approximation of DSRG-MRPT2 based on CASSCF. We demonstrate the application of the ASCI-DSRG-MRPT2 method in evaluations of the spin-state energy gaps in iron porphyrins, polyacenes, and periacenes along with the reaction energies of methane oxidation by FeO + and electrocyclic ring formation in cethrene.