Max-Planck-Institut für Chemische Energiekonversion, Stiftstr. 34-36, 45470 Mülheim an der Ruhr, Germany.
Department of Organic Chemistry, University of Chemistry and Technology, Prague, Technická 5, 166 28 Prague 6, Czech Republic.
J Chem Phys. 2017 Nov 7;147(17):174104. doi: 10.1063/1.5001320.
The similarity transformed equation of motion coupled-cluster approach is extended for applications to high-spin open-shell systems, within the unrestricted Hartree-Fock (UHF) formalism. An automatic active space selection scheme has also been implemented such that calculations can be performed in a black-box fashion. It is observed that both the canonical and automatic active space selecting similarity transformed equation of motion (STEOM) approaches perform about as well as the more expensive equation of motion coupled-cluster singles doubles (EOM-CCSD) method for the calculation of the excitation energies of doublet radicals. The automatic active space selecting UHF STEOM approach can therefore be employed as a viable, lower scaling alternative to UHF EOM-CCSD for the calculation of excited states in high-spin open-shell systems.
相似变换的运动方程耦合簇方法被扩展到应用于高自旋开壳体系,在非限制的哈特ree-fock(UHF)形式。一个自动的活动空间选择方案也已经实现,使得计算可以以黑盒的方式进行。结果表明,对于双自由基激发能的计算,正则和自动的活性空间选择相似变换的运动方程(STEOM)方法的表现与更昂贵的运动方程耦合簇单双(EOM-CCSD)方法相当。因此,自动活性空间选择 UHF STEOM 方法可以作为一种可行的、更低规模的替代方法,用于计算高自旋开壳体系中的激发态。