In the present paper, we have studied the temperature dependence of translational diffusion and solvation dynamics of a dissolved dipolar dye in the nonionic acetamide-urea deep eutectic solvent (DES), to characterize the viscosity coupling of the measured relaxation times and verify the dynamical heterogeneity aspect of this medium. Three different time-resolved experimental techniques have been employed for this purpose: fluorescence correlation spectroscopy, transient absorption (TA) spectroscopy, and optical Kerr effect (OKE) spectroscopy. The first method provides the proof that the translational diffusion time of a solute in acetamide-urea DES [CHCONH + (1 - )CO(NH), = 0.6] exhibits a fractional viscosity dependence, with exponent 0.758, which, when compared with the viscosity-diffusion relationship for the same solute in common molecular solvents, suggests moderate deviation from the Stokes-Einstein relation. Stokes shift dynamics of a solvatochromic dye, 4-(dicyanomethylene)-2-methyl-6-(4-dimethylaminostyryl)-4-pyran in this DES, followed via femtosecond TA measurements, have been found to be triexponential in nature and dominated by a ∼100 fs component. The other two components, which contribute to a total dynamic Stokes shift magnitude of ∼2500 cm, are characterized by time constants in the ∼5 and ∼50 ps regimes. Subsequent comparison with the femtosecond OKE measurements suggests that the relatively slower picosecond solvation components originate from the rapid reorientation of the solvent molecules, while the subpicosecond solvation response arises from the participation of the collective low-frequency solvent modes (such as intermolecular vibrations and librations). We find that the rotational diffusion lifetimes also exhibit fractional power dependence on medium viscosity and thus deviate from the Stokes-Einstein-Debye pprediction. All of these results therefore suggest that the nonionic acetamide-urea DES is a moderately heterogeneous medium.
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http://dx.doi.org/10.1021/acs.jpcb.9b07794 | DOI Listing |
J Am Chem Soc
December 2024
Department of Chemistry, University of Nevada, Reno, 1664 N. Virginia Street, Reno, Nevada 89557, United States.
Hydration dynamics and solvent viscosity play critical roles in the structure and function of biomolecules. An overwhelming body of evidence suggests that protein and membrane fluctuations are closely linked to solvent fluctuations. While extensive research exists on the use of vibrational probes to detect local interactions and solvent dynamics, fewer studies have explored how the behavior of these reporters changes in response to bulk viscosity.
View Article and Find Full Text PDFPhys Chem Chem Phys
December 2024
Univ. Bordeaux, CNRS, Bordeaux INP, Institut des Sciences Moléculaires, UMR 5255, F-33400 Talence, France.
The effect of conformational dynamics and solvent interactions on the second-order nonlinear optical (NLO) responses of the open and closed forms of a donor-acceptor Stenhouse adduct (DASA) are investigated by a mixed quantum/classical computational approach, which couples molecular dynamics (MD) simulations and time-dependent density functional theory (TD-DFT) calculations. The latter are further combined with various solvation schemes, including polarizable continuum models, hybrid QM/MM approaches using either non polarizable or polarizable electrostatic embedding, and QM/QM' schemes with explicit treatment of a few molecules of the first solvation shell. The performances of the different solvation models are discussed in the context of comparisons with experimental data obtained from hyper-Rayleigh scattering measurements.
View Article and Find Full Text PDFACS Phys Chem Au
November 2024
Scuola Normale Superiore, Piazza dei Cavalieri 7, 56126 Pisa, Italy.
A novel fully atomistic multiscale classical approach to model the optical response of solvated real-size plasmonic nanoparticles (NPs) is presented. The model is based on the coupling of the Frequency Dependent Fluctuating Charges and Fluctuating Dipoles (ωFQFμ), specifically designed to describe plasmonic substrates, and the polarizable Fluctuating Charges (FQ) classical force field to model the solvating environment. The resulting ωFQFμ/FQ approach accounts for the interactions between the radiation and the NP, as well as with the surrounding solvent molecules, by incorporating mutual interactions between the plasmonic substrate and solvent.
View Article and Find Full Text PDFNat Commun
December 2024
Mechanical Engineering Department, Stanford University, Stanford, CA, 94305, USA.
Supercritical fluids exhibit distinct thermodynamic and transport properties, making them of particular interest for a wide range of scientific and engineering applications. These anomalous properties emerge from structural heterogeneities due to the formation of molecular clusters at conditions above the critical point. While the static behavior of these clusters and their effects on the thermodynamic response functions have been recognized, the relation between the ultrafast cluster dynamics and transport properties remains elusive.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Department of Chemical and Biomolecular Engineering, National University of Singapore 4 Engineering Drive 4, 117585, Singapore.
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