Concerted Ion and Electron Transfer Across Electronically Conductive Polymer Membranes

1992 ◽  
Vol 293 ◽  
Author(s):  
Charles R. Martin ◽  
Del R. Lawson ◽  
Wenbin Liang

AbstractWe describe in this paper an experiment involving an electronically conductive polymer (ECP) which, to our knowledge, has not been described previously. A free-standing ECP (polypyrrole)-based membrane separates a solution of an electron donor from a solution of an electron acceptor. Because the ECP is both electronically and anionically conductive, the membrane can transport electrons from the donor solution to the acceptor solution, and anions in the opposite direction, such that a sustainable electron-transfer reaction is driven across the ECP membrane. We demonstrate such transmembrane electron/ion-transfer processes using both an inorganic and a biochemical electron donor/acceptor system. The biochemical case is of particular interest because we show that the reduced form of the enzyme glucose oxidase can give its electrons directly to the synthetic metal. Direct electron transfer is usually not possible at inorganic metals.

2004 ◽  
Vol 08 (09) ◽  
pp. 1118-1128 ◽  
Author(s):  
Bhaskar G. Maiya

This article reviews recent developments that have taken place in research related to new porphyrin architectures and their host-guest chemistry, as described in a microsymposium bearing the same name held during the 3rd International Conference on Porphyrins and Phthalocyanines (ICPP-3). The usefulness of representative arrays, aggregates, donor-acceptor systems, and receptor motifs based on porphyrin architectures is highlighted as it applies to the fabrication of molecular devices, understanding the biomimetic electron transfer processes, and recognition of bioorganic substrates.


2017 ◽  
Vol 19 (21) ◽  
pp. 13596-13603 ◽  
Author(s):  
J. Ahrens ◽  
M. Frank ◽  
G. H. Clever ◽  
D. Schwarzer

Photo-excitation of self-assembled palladium based coordination cages consisting of phenothiazine electron donor and anthraquinone electron acceptor ligands produce charge separated states with lifetimes of up to 1.5 ns.


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