We note that the effects of anharmonicity are practically impossible to be computed with DFT for large systems

of interest to biology. Intensities of IR as well as Raman modes can, however, be obtained straightforwardly. Theoretical studies on a model of the oxygen evolving complex of PS II have demonstrated how computed vibrational RG7112 solubility dmso frequencies can provide valuable feedback for the interpretation of experimental data. Specifically, calculations by Gascon et al. (2007) suggested selleck chemical that the vibrational modes of carboxylate groups ligated to manganese ions of the OEC might be insensitive to changes in the formal oxidation states of the ions because of electron delocalization within the cluster. At the same time, it was shown that the charge rearrangement associated with the S-state transitions in the OEC might induce shifts in the vibrational frequency of carboxylate groups

that do not function as direct ligands to the manganese ions. These theoretical results imply that the vibrational frequency shifts observed in experimental FTIR measurements do not necessarily have to be interpreted as reflecting changes in the first coordination sphere of the Mn cluster, thus providing ways to reconcile the perceived discrepancies between FTIR and XRD data (Sproviero et al. 2008b). Optical spectra Density functional theory is restricted from its foundations to ground states only; therefore, the calculation of excited states and their properties has to be approached indirectly. click here This is achieved using time-dependent linear response theory, in which one studies the frequency dependence of a time-dependent electric field perturbation, the poles of which provide excitation

energies. Thus, time-dependent DFT (TD-DFT) calculations yield the transition energy rather than the total energy of the excited state, which therefore is never explicitly calculated (Bauernschmitt and Ahlrichs 1996; Casida et al. 1998; Stratmann et al. 1998). It should be noted that the TD-DFT approach allows also for a full determination of the central quantities involved in the calculation of both absorption Dapagliflozin and circular dichroism (CD) spectra. It is also possible to predict magnetic circular dichroism (MCD) spectra through TD-DFT calculations (Seth et al. 2004, 2005; Seth and Ziegler 2006), although ab initio multireference approaches are preferred in this respect since they explicitly cover the correct physics involved (Ganyushin and Neese 2008). Optical spectra predicted by TD-DFT with the use of either the BP86 or B3LYP functionals may occasionally be of acceptable quality (Fiedler et al. 2005; Jackson et al. 2005; Schenker et al. 2005; Stich et al. 2005) even though many problematic cases and a multitude of artifacts plague this methodology (Grapperhaus et al. 2001; Neese 2008a).