4.5 Article

Dynamics of a PEG based non-ionic deep eutectic solvent: Temperature dependence

Journal

FLUID PHASE EQUILIBRIA
Volume 448, Issue -, Pages 22-29

Publisher

ELSEVIER
DOI: 10.1016/j.fluid.2017.05.003

Keywords

Non-ionic DES; Acetamide; Urea; Polyethylene glycol (PEG); Dielectric relaxation; Time-resolved fluorescence measurements

Funding

  1. Council for Scientific and Industrial Research (CSIR), India
  2. ET acknowledges DST, India
  3. S. N. Bose Centre through the 12th five-year plan project High Precision Spectro-Microscopy of Novel Materials [SNB/AB/12-13/96]

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Temperature dependent dynamics of a polyethylene glycol based non-ionic deep eutectic solvent (DES) has been investigated via both dielectric relaxation spectroscopic (DRS), and time-resolved fluorescence (TRF) Stokes shift and anisotropy measurements. The composition of the DES considered is as follows: w[fCH(3)CONH(2) + (1- f)NH2CONH2] + (1 w)PEG, where w represents the weight fraction and f represents the mole fraction. In this investigation we have kept w fixed at 0.67 and f fixed at 0.6. Both DR and TRF measurements have been carried out within the temperature range, 308 <= T(K) <= 333. DRS measurements have been performed within the frequency window, 0.2 <= v/GHz <= 50. TRF measurements employ coumarin 153 (C153), a fluorescent probe molecule, as a local reporter. Interestingly, the estimated static dielectric constant (epsilon(0)) for this DES is considerably large, even higher than the e0 value of polar solvents like, dimethyl formamide and acetonitrile. Measured DR spectra require four relaxation processes, spread over sub-10 ps to nanosecond time regime, to adequately describe the detected DR dynamics of this DES. Surprisingly, this non-ionic DES possesses a nanosecond relaxation component similar to that in ionic acetamide DESs. The presence of this slow relaxation component is further supported by the corresponding dynamic fluorescence Stokes shifts measurements. Both DR and dynamic fluorescence anisotropy data reveal substantial fractional viscosity dependence for solute rotation in this DES. (C) 2017 Elsevier B.V. All rights reserved.

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