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We have also calculated such "bond-constrained" E(st) values by adjusting the bond lengths for the uncoordinated (gas-phase) species so to match the field-dependent equilibrium values for the chemisorbates. This alternative approach therefore adjusts the (internal) steric repulsion in the isolated species to match that for the chemisorbate, rather than vice versa. Interestingly, the E(st) values obtained with either of the "bond-constrained" approaches are comparable (chiefly within 0.5 eV). This supports the notion that at least an approximate distinction can be made between steric-repulsion components associated with the internal chemisorbate, and metal-chemisorbate bonds.
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note
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This differs from the (CSOV) analysis of Bagus et al. (Ref. 47) in which the subset of the full orbital space in which the orbitals are allowed to vary, and hence constitute a particular contribution, corresponding to the (virtual) orbital space of the fragments, whereas in the ADF analysis they refer to the (virtual) orbital spaces of the irreducible representations of the system's symmetry group.
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