Electron-driven proton transfer enables nonradiative photodeactivation in microhydrated 2-aminoimidazole. (20th September 2018)

• Record Type: Journal Article
• Authors: Janicki, Mikołaj J.; Szabla, Rafał; Šponer, Jiří; Góra, Robert W.
• Is Part Of: Faraday discussions. Volume 212(2019)
• Page Start: 345
• Page End: 358
• Publication Date: 2018-09-20
• Subjects: Chemistry -- Periodicals; Metallurgy -- Periodicals; Electrochemistry -- Periodicals; 540
• DOI: 10.1039/c8fd00086g
• Languages: English
• ISSNs: 1359-6640

Abstract

Abstract : Prebiotically credible activator of non-enzymatic RNA template-copying, 2-aminoimidazole, is protected from destructive photochemistry by photoacidity. Abstract : 2-Aminoimidazole (2-AIM) was proposed as a plausible nucleotide activating group in a nonenzymatic copying and polymerization of short RNA sequences under prebiotically plausible conditions. One of the key selection factors controlling the lifespan and importance of organic molecules on early Earth was ultraviolet radiation from the young Sun. Therefore, to assess the suitability of 2-AIM for prebiotic chemistry, we performed non-adiabatic molecular dynamics simulations and static explorations of potential energy surfaces of the photoexcited 2-AIM–(H2 O)5 model system by means of the algebraic diagrammatic construction method to the second order [ADC(2)]. Our quantum mechanical simulations demonstrate that 1 πσ* excited states play a crucial role in the radiationless deactivation of the UV-excited 2-AIM–(H2 O)5 system. More precisely, electron-driven proton transfer (EDPT) along water wires is the only photorelaxation pathway leading to the formation of 1 πσ*/S0 conical intersections. The availability of this mechanism and the lack of destructive photochemistry indicate that microhydrated 2-AIM is characterized by substantial photostability and resistance to prolonged UV irradiation.