Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/154728
Title: Polyterthiophenes cross-linked with terpyridyl metal complexes for molecular architecture of optically and electrochemically tunable materials
Authors: Wagner, Michal
Wagner, Klaudia
Barnsley, Jonathan E.
Veksha, Andrei
Wagner, Paweł
Gordon, Keith C.
Bobacka, Johan
Wallace, Gordon G.
Ivaska, Ari
Officer, David L.
Lisak, Grzegorz
Keywords: Science::Chemistry
Issue Date: 2020
Source: Wagner, M., Wagner, K., Barnsley, J. E., Veksha, A., Wagner, P., Gordon, K. C., Bobacka, J., Wallace, G. G., Ivaska, A., Officer, D. L. & Lisak, G. (2020). Polyterthiophenes cross-linked with terpyridyl metal complexes for molecular architecture of optically and electrochemically tunable materials. ChemElectroChem, 7(21), 4453-4459. https://dx.doi.org/10.1002/celc.202001142
Journal: ChemElectroChem
Abstract: Novel conductive polymer-based metal complexes were electrochemically synthesized and characterized in relation to (spectro)electrochemical stimuli. Particularly, we focused our attention on terthiophenes functionalized with terpyridine groups, along with Fe2+ cations present during electrochemical synthesis. The resultant electroactive films are coherent, robust, and exhibit mixed absorption profiles upon electrochemical doping, characteristic for both polyterthiophenes and metal-ligand transitions. At certain oxidation potentials, the formation of radical cation and also dication states were observed. The latter, influence the optical transitions related to metal centers, and can reversibly be everted by switching to lower potentials. Furthermore, the polymer “cross-linking metal” can be removed from the structure, which we obtained by partial exchange of Fe2+ with Cu2+ and Zn2+ cations. The conducted cation exchange studies however elucidate the complexity and difficulty of such an approach. With future electropolymerization “strategies” we are expecting to extend film stability during application of relatively high potentials, as well as in the interim of cation exchange.
URI: https://hdl.handle.net/10356/154728
ISSN: 2196-0216
DOI: 10.1002/celc.202001142
Rights: © 2020 Wiley-VCH GmbH. All rights reserved.
Fulltext Permission: none
Fulltext Availability: No Fulltext
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