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- W2548008265 abstract "In this work, we demonstrate the use of broad-band pump-probe spectroscopy to measure femtosecond solvation dynamics. We report studies of a rhodamine dye in methanol and cryptophyte algae light-harvesting proteins in aqueous suspension. Broad-band impulsive excitation generates a vibrational wavepacket that oscillates on the excited-state potential energy surface, destructively interfering with itself at the minimum of the surface. This destructive interference gives rise to a node at a certain probe wavelength that varies with time. This reveals the Gibbs free-energy changes of the excited-state potential energy surface, which equates to the solvation time correlation function. This method captures the inertial solvent response of water (∼40 fs) and the bimodal inertial response of methanol (∼40 and ∼150 fs) and reveals how protein-buried chromophores are sensitive to the solvent dynamics inside and outside of the protein environment." @default.
- W2548008265 created "2016-11-11" @default.
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- W2548008265 date "2016-11-09" @default.
- W2548008265 modified "2023-09-27" @default.
- W2548008265 title "Broad-Band Pump–Probe Spectroscopy Quantifies Ultrafast Solvation Dynamics of Proteins and Molecules" @default.
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