Understanding the Photoprocesses in Biological Systems: Need for Accurate Multireference Treatment.

Light-matter interaction is crucial to life itself and revolves around many of the central processes in biology. The need for understanding these photochemical and photophysical processes cannot be overemphasized. Interaction of light with biological systems starts with the absorption of light and subsequent phenomena that occur in the excited states of the system. However, excited states are typically difficult to understand within the mean field approximation of quantum chemical methods. Therefore, suitable multireference methods and methodologies have been developed to understand these phenomena. In this Perspective, we will describe a few methods and methodologies suitable for these descriptions and discuss some persisting difficulties.

Conformational Effects on the Absorption Spectra of Phytochromes.

Bacteriophytochrome is a photoreceptor protein that contains the biliverdin (BV) chromophore as its active component. The spectra of BV upon mutation remain remarkably unchanged, as far as spectral positions are concerned. This points toward the minimal effect of electrostatic effects on the electronic structure of the chromophore. However, the relative intensities of the Q and Soret bands of the chromophore change dramatically upon mutation. In this work, we delve into the molecular origin of this unusual intensity modulation. Using extensive classical MD and QM/MM calculations, we show that due to mutation, the conformational population of the chromophore changes significantly. The noncovalent interactions, especially the stacking interactions, lead to extra stabilization of the cyclic form in the D207H mutated species as opposed to the open form in the wild-type BV. Thus, unlike the commonly observed direct electrostatic effect on the spectral shift, in the case of BV the difference observed is in varying intensities, and this in turn is driven by a conformational shift due to enhanced stacking interaction.

Mechanism of Singlet Fission in Carotenoids from a Polyene Model System.

Singlet fission (SF) is the process of formation of multiple excitons (triplet) from a locally excited singlet state. The mechanism of SF in polyacenes has been shown to proceed via a charge transfer intermediate state. However, carotenoids are not understood in the context of SF. This is possibly due to the complicated multireference nature of the low-lying excited states of carotenoids and the presence of a dark 21Ag state below the optically bright 1Bu state. In this work, we show that the dark Ag state in polyenes and/or carotenoids, along with the charge transfer states, plays a pivotal role in the SF process. We notice that the relative importance of these states varies with a change in geometry and the overall presence of multiple pathways is crucial to the success of the SF process in carotenoid aggregates and disordered geometries.