Pathways of viologen-mediated oxidation-reduction reactions across dihexadecyl phosphate bilayer membranes

Journal Article · Thu Jan 14 04:00:00 EST 1993 · Journal of Physical Chemistry; (United States)

DOI:https://doi.org/10.1021/j100104a030· OSTI ID:6389661

Patterson, B C; Hurst, J K ^[1]

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1. Oregon Graduate Inst. of Science and Technology, Beaverton (United States)

Transmembrane reduction of methylviologen (N,N-dimethyl-4,4[prime]-bipyridinium, MV[sup 2+]) and several n-alkylmethyl analogs, i.e., N-alkyl-N[prime]-methyl-4,4[prime]-bipyridinium, (C[sub n]MV[sup 2+],n[le]10), entrapped within dihexadecyl phosphate (DHP) vesicles by S[sub 2]O[sub 4][sup 2[minus]] located in the bulk aqueous phase occurred only when viologens were also initially present on the same side of the membrane as the reductant. Viologen radical cation formation was biphasic, with the reduction of the externally bound viologen dications preceding reduction of the entrapped viologen. Transmembrane reduction was accompanied by comigration of a viologen radical cation with each electron transferred across the bilayer. The MV[sup +] ion formed on the external surface was monomeric, but the MV[sup +] formed internally was aggregated (or multimeric); from the wavelength dependence of the kinetic curves, it was shown that aggregation coincided with or rapidly followed the rate-limiting transmembrane redox step. For the C[sub n]MV[sup 2+] ions, the reaction dynamics were qualitatively similar but were complicated by the simultaneous presence of both monomeric and multimeric forms of C[sub n]MV[sup +] at the outer vesicle interface. When n>10, reduction of external C[sub n]MV[sup 2+] reaction medium also contained lipophilic ions, under which conditions all of the internal ions could be reduced. Correspondingly, only one-third of the external C[sub 16]MV[sup 2+] translocated to the inner vesicle surface. Computer simulations of the complex kinetic waveforms required inclusion of two independent transmembrane redox steps to obtain adequate data fits. These were interpreted in terms of two distinct reaction pathways involving (i) transverse diffusion of interfacially bound reactants and (ii) electron tunneling between the viologen radical cations and dications juxtaposed in the opposite bilayer leaflets. 48 refs., 8 figs., 4 tabs.

• OSTI ID: 6389661
• Journal Information: Journal of Physical Chemistry; (United States), Journal Name: Journal of Physical Chemistry; (United States) Vol. 97:2; ISSN JPCHAX; ISSN 0022-3654
• Country of Publication: United States
• Language: English

Related Subjects

14 SOLAR ENERGY
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37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
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AZINES
BIPYRIDINES
CHARGED PARTICLES
CHEMICAL REACTION KINETICS
CHEMICAL REACTIONS
DIFFUSION
DYNAMICS
HETEROCYCLIC COMPOUNDS
IONS
KINETICS
MECHANICS
MEMBRANES
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
OXIDATION
PYRIDINES
RADICALS
REACTION KINETICS
REDUCTION
TUNNELING