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• W2896105526 endingPage "8538" @default.
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• W2896105526 abstract "The microsolvation and photophysics of 3-amino-1,2,4-triazole (3AT) after excitation to the light-absorbing S2(nπ*) state were studied by using resonance Raman spectroscopy and single component artificial force-induced reaction (SC-AFIR) in a global reaction route mapping (GRRM) strategy. The vibrational spectra were assigned on the basis of experimental data and density functional theory (DFT) calculations. The resonance Raman spectra of 3AT were measured to probe the excited state structural dynamics in the Franck–Condon region. The conformations of 3AT(CH3CN)1, 3AT(CH3OH)2, and 3AT(H2O)2 clusters were determined by combining vibrational spectrum experiments and B3LYP/6-311++G(d,p) computations. DFT calculations were carried out to obtain the minimal excitation energies of the lower-lying singlet excited states, and the curve-crossing points. It was revealed that the short-time structural dynamics of 3AT were dominated by the N–N stretching coordinates. An excited state decay mechanism is proposed: 3AT is initially excited to the S2(nπ*) state, then the conical intersection (CI) of the S2(nπ*)/S1(ππ*) potential energy surfaces is crossed, and 3AT then decays to the lower solvent-dependent excited state S1(ππ*). It subsequently returns to the S0 state, accompanied by a large Stokes fluorescence shift, which was interpreted as the stabilized S1(ππ*) excited state bonding to several water molecules via intermolecular hydrogen bonding." @default.
• W2896105526 created "2018-10-26" @default.
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• W2896105526 date "2018-10-08" @default.
• W2896105526 modified "2023-10-13" @default.
• W2896105526 title "UV–Vis, Fluorescence, and Resonance Raman Spectroscopic and Density Functional Theoretical Studies on 3-Amino-1,2,4-triazole: Microsolvation and Solvent-Dependent Nonadiabatic Excited State Decay in Solution" @default.
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• W2896105526 doi "https://doi.org/10.1021/acs.jpca.8b07384" @default.
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• W2896105526 hasPublicationYear "2018" @default.
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