Activity space

So-called complete active space (CAS) methods fomi all CSFs that... 

Roos B O, Taylor P R and Siegbahn P E M 1980 A complete active space SCF method (CASSCF) using a density matrix formulated super-CI approach Chem. Phys. 48 157-73... 

Roos B O 1987 The complete active space self-consistent field method and its applications in electronic structure calculations Adv. Chem. Phys. 69 399-445... 

The wave function for the elechonic structure can in principle be any of the constructions employed in electronic structure theoiy. The prefened choice in this context is a wave funchons that can be classified as single and multi-configurational, and for the latter type only complete active space (CAS) wave... 

Some details of END using a multiconfigurational electronic wave function with a complete active space (CASMC) have been introduced in terms of an orthonormal basis and for a fixed nuclear framework [25], and were recently [26] discussed in some detail for a nonoithogonal basis with electron translation factors. 

Diverse libraries can be used for lead finding by screening against several different targets. The selected compounds should cover the biological activity space well. 

Complete active space self-consistent field... 

So-ealled complete-active-space (CAS) methods form all CSFs that ean be ereated by distributing N valenee eleetrons among P valenee orbitals. For example, the eight non-eore eleetrons of H2O might be distributed, in a manner that gives Ms = 0, among six... 

Unfortunately, these methods require more technical sophistication on the part of the user. This is because there is no completely automated way to choose which configurations are in the calculation (called the active space). The user must determine which molecular orbitals to use. In choosing which orbitals to include, the user should ensure that the bonding and corresponding antibonding orbitals are correlated. The orbitals that will yield the most correlation... 

An MCSCF calculation in which all combinations of the active space orbitals are included is called a complete active space self-consistent held (CASSCF) calculation. This type of calculation is popular because it gives the maximum correlation in the valence region. The smallest MCSCF calculations are two-conhguration SCF (TCSCF) calculations. The generalized valence bond (GVB) method is a small MCSCF including a pair of orbitals for each molecular bond. 

In this exercise, we will introduce the Complete Active Space Multiconfiguration SCF (CASSCF) method, using it to compute the excitation energy for the first excited state of acrolein (a singlet). The CIS job we ran in Exercise 9.3 predicted an excitation energy of 4.437 eV, which is rather for from the experimental value of 3.72 eV. We ll try to improve this prediction here. 

A CASSCF calculation is a combination of an SCF computation with a full Configuration Interaction calculation involving a subset of the orbitals. The orbitals involved in the Cl are known as the active space. In this way, the CASSCF method optimizes the orbitals appropriately for the excited state. In contrast, the Cl-Singles method uses SCF orbitals for the excited state. Since Hartree-Fock orbitals are biased toward the ground state, a CASSCF description of the excited state electronic configuration is often an improvement. 

A CASSCF calculation is requested in Gaussian with the CASSCF keyword, which requires two integer arguments the number of electrons and the number of orbitals in the active space. The active space is defined assuming that the electrons come from as many of the highest occupied molecular orbitals as are needed to obtain the specified number of electrons any remaining required orbitals are taken from the lowest virtual orbitals. 

For example, in a 4-electron, 6-orbital CAS—specified as CASSCF 4,6)—performed on a singlet system, the active space would consist of the two highest occupied molecular orbitals (where the four electrons reside) and the four lowest virtual orbitals. Similarly, for a 6-electron, 5-orbital CAS on a triplet system, the active space would consist of the four highest occupied MO s— two of which are doubly-occupied and two are singly-occupied—and the LUMO (the keyword is CASSCF(6,5)). 

The GuesssAlter keyword is used to ensure that the orbitals of interest are included in the active space. This keyword allows orbitals to be swapped in order within the initial guess. A prior run with Gue s=Only and/or Pop=Full can be used to quickly determine the orbital symmetries and decide which ones should be placed within the active space. 

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