Rubber-elasticity and electrochemical activity of iron(ii) tris(bipyridine) crosslinked poly(dimethylsiloxane) networks

2,2'-Bipyridine-terminated poly(dimethylsiloxane)s (bpyPDMS) with number average molecular weights, M , of 3300, 6100, 26 200, and 50 000 g mol were synthesized. When mixed with Fe(BF ) at low concentrations, red solutions formed with UV-vis spectra that match those of iron(ii) tris(2,2'-b...

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Veröffentlicht in:Soft matter 2017-09, Vol.13 (37), p.6542-6554
Hauptverfasser: Williams, Zachary H, Burwell, Emily D, Chiomento, Ambre E, Demsko, Kyle J, Pawlik, Jacob T, Harris, Shannon O, Yarolimek, Mark R, Whitney, Megan B, Hambourger, Michael, Schwab, Alexander D
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Sprache:eng
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Zusammenfassung:2,2'-Bipyridine-terminated poly(dimethylsiloxane)s (bpyPDMS) with number average molecular weights, M , of 3300, 6100, 26 200, and 50 000 g mol were synthesized. When mixed with Fe(BF ) at low concentrations, red solutions formed with UV-vis spectra that match those of iron(ii) tris(2,2'-bipyridine) (Fe(bpy) ). Upon solvent evaporation, Fe(bpy) crosslinked PDMS networks (bpyPDMS/Fe(ii)) formed, and were studied using oscillating shear rheometry. The shear storage moduli (0.084 to 2.6 MPa) were found to be inversely proportional to the M of the PDMS, though the storage moduli at low molecular weights greatly exceeded the storage moduli of comparable covalently crosslinked PDMS networks. The shear storage moduli exhibited the characteristic rubbery plateau up to ∼135 °C. Films of bpyPDMS/Fe(ii) coated onto electrodes were found to be electrochemically active, especially so when the PDMS M is low. The Fe(bpy) crosslinks can be reversibly oxidized over ∼500 nm away from the electrode surface in the presence of a suitable electrolyte.
ISSN:1744-683X
1744-6848
DOI:10.1039/c7sm01169e