Chem. Phys. 000, 000000 (201x).
(Received xx XXX 2011; accepted xx XXX 2011)
An implementation of analytical gradients, transition moments and excited state properties for scaled opposite-spin (SOS) CC2 and a SOS variant of the algebraic diagrammatic construction through second order ADC(2) is presented. The time-determining fifth order scaling steps in the algorithms are replaced by schemes with only fourth order scaling computational costs using a ``resolution of the identity'' approximation for the electron repulsion integrals and a Laplace transformation of the orbital energy denominators. This leads to a significant reduction of computational costs for geometry optimizations of large systems. This work is an extension to the recently presented quartic scaling algorithm for SOS-CC2 energies for ground and excited states. The Laplace error for adiabatic electronic excitation energies and excited state structures is found to be very small. SOS-ADC(2) provides for adiabatic electronic excitation energies, excited state structure parameters, harmonic vibrational frequencies as well as dipole moments and transition strengths a similar accuracy than SOS-CC2. Timings for ground and excited state calculations are reported and applications to a chlorophyll molecule and a 2,2':6',2''-bis(terpyridine) with 160 atoms demonstrate how the new implementation extends the applicability of these methods for large systems.
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