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Title: Permeability and partitioning of ferrocene ethylene oxide and propylene oxide oligomers into electropolymerized films from acetonitrile and polyether solutions

Journal Article · · Journal of Physical Chemistry; (United States)
DOI:https://doi.org/10.1021/j100094a023· OSTI ID:6717729
;  [1]
  1. Univ. of North Carolina, Chapel Hill, NC (United States)

We report the first electrochemically-based measurements of the rates of small polymer permeation into another polymer. The small polymer permeants are ferrocene ethylene oxide oligomers containing 2, 7, and 16 units and a propylene oxide oligomer containing 3 units. Their permeation into ultrathin microelectrode-supported films of the metal complex polymer poly[Ru(vbpy)[sub 3]](ClO[sub 4])[sub 2] was measured from acetonitrile solutions and from solutions in a methyl-endcapped ethylene oxide oligomer, MPEG-400 (MW = 400). Permeations of other ferrocenes with bulky substituents were also measured from acetonitrile solutions. In all cases the permeability, PD[sub POL], into poly[Ru(vbpy)[sub 3]](ClO[sub 4])[sub 2] films is strongly dependent on the permeant molecular volume. Direct measurement of the partition coefficient, P, in acetonitrile shows that permeability variations among a series of related permeants are controlled more by variations in P than by diffusivity in the poly[Ru(vbpy)[sub 3]](ClO[sub 4])[sub 2] phase. Permeation of ferrocene polyether oligomers is much slower from MPEG-400 solutions than from acetonitrile; this appears to arise more from a decrease in D[sub POL] than from one of P. 19 refs., 4 figs., 2 tabs.

OSTI ID:
6717729
Journal Information:
Journal of Physical Chemistry; (United States), Vol. 98:43; ISSN 0022-3654
Country of Publication:
United States
Language:
English