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- W2204754827 abstract "N-alkylated indanylidene pyrroline Schiff bases (NAIPs) are of great interest because their photoisomerization mimics the primary photoreactions of the retinal chromophore in rhodopsin. The nonadiabatic dynamics of two NAIP models (OMe-NAIP and dMe-OMe-NAIP) are investigated by trajectory surface-hopping method at the semi-empirical OM2/MRCI level. Both molecules show ultrafast isomerization governed by nonadiabatic dynamics via the S0/S1 conical intersections (CIs). Two CIs, CIα and CIβ, play important roles in the E → Z and Z → E isomerization dynamics, respectively, and are mainly distinguished by different twisting statuses of the central C1′–C4 double bond. Although both compounds show ultrafast nonadiabatic dynamics, the S1 lifetime of dMe-OMe-NAIP is much longer than that of OMe-NAIP. By removing the methyl group, dMe-OMe-NAIP allows less twist at the C1′–C4 double bond than OMe-NAIP. This result in the slower excited-state decay of dMe-OMe-NAIP, providing solid evidence to support a similar hypothesis proposed in a previous study." @default.
- W2204754827 created "2016-06-24" @default.
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- W2204754827 date "2015-12-01" @default.
- W2204754827 modified "2023-10-17" @default.
- W2204754827 title "Nonadiabatic dynamics and photoisomerization of biomimetic photoswitches" @default.
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- W2204754827 doi "https://doi.org/10.1016/j.chemphys.2015.10.003" @default.
- W2204754827 hasPublicationYear "2015" @default.
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