How Methylation Modifies the Photophysics of the Native All-trans-Retinal Protonated Schiff Base: A CASPT2/MD Study in Gas Phase and in Methanol
journal contributionposted on 28.02.2018 by Rute Barata-Morgado, M. Luz Sánchez, Aurora Muñoz-Losa, M. Elena Martín, Francisco J. Olivares del Valle, Manuel A. Aguilar
Any type of content formally published in an academic journal, usually following a peer-review process.
A comparison between the free-energy surfaces of the all-trans-retinal protonated Schiff base (RPSB) and its 10-methylated derivative in gas phase and methanol solution is performed at CASSCF//CASSCF and CASPT2//CASSCF levels. Solvent effects were included using the average solvent electrostatic potential from molecular dynamics method. This is a QM/MM (quantum mechanics/molecular mechanics) method that makes use of the mean field approximation. It is found that the methyl group bonded to C10 produces noticeable changes in the solution free-energy profile of the S1 excited state, mainly in the relative stability of the minimum energy conical intersections (MECIs) with respect to the Franck–Condon (FC) point. The conical intersections yielding the 9-cis and 11-cis isomers are stabilized while that yielding the 13-cis isomer is destabilized; in fact, it becomes inaccessible by excitation to S1. Furthermore, the planar S1 minimum is not present in the methylated compound. The solvent notably stabilizes the S2 excited state at the FC geometry. Therefore, if the S2 state has an effect on the photoisomerization dynamics, it must be because it permits the RPSB population to branch around the FC point. All these changes combine to speed up the photoisomerization in the 10-methylated compound with respect to the native compound.