Kinetics and solvent-dependent thermodynamics of water capture by a fullerene-based hydrophobic nanocavity.

نویسندگان

  • Michael Frunzi
  • Anne M Baldwin
  • Nobuyuki Shibata
  • Sho-Ichi Iwamatsu
  • Ronald G Lawler
  • Nicholas J Turro
چکیده

Kinetic and thermodynamic properties of water encapsulation from organic solution by an open-cage [60]fullerene derivative have been investigated. 2D exchange NMR spectroscopy (EXSY) measurements were employed to determine the association and dissociation constants at 300-330 K (k(a) = 4.3 M(-1) × s(-1) and k(d) = 0.42 s(-1) at 300 K) in 1,1,2,2-tetrachloroethane-d(2) as well as the activation energies (E(a,ass) = 27 kJ mol(-1), E(a,diss) = 50 kJ mol(-1)). The equilibrium constants and thermodynamic parameters in various solvents (benzene-d(6), 1,2-dichlorobenzene-d(4), and dimethylsulfoxide-d(6)) were estimated using 1D-(1)H NMR spectroscopy. The parameters were dependent on the polarity of the solvent; ΔH depended linearly on the solvent polarity, becoming increasingly unfavorable as polarity increased. Mixtures of polar dimethylsulfoxide-d(6) in less polar 1,1,2,2-tetrachloroethane-d(2) showed a similar trend.

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عنوان ژورنال:
  • The journal of physical chemistry. A

دوره 115 5  شماره 

صفحات  -

تاریخ انتشار 2011