Redox-Rich Metallocene Tetrazene Complexes : Synthesis, Structure, Electrochemistry, and Catalysis
| dc.contributor.author | Vanicek, Stefan | |
| dc.contributor.author | Jochriem, Markus | |
| dc.contributor.author | Hassenrück, Christopher | |
| dc.contributor.author | Roy, Souvik | |
| dc.contributor.author | Kopacka, Holger | |
| dc.contributor.author | Wurst, Klaus | |
| dc.contributor.author | Müller, Thomas | |
| dc.contributor.author | Winter, Rainer F. | |
| dc.contributor.author | Reisner, Erwin | |
| dc.contributor.author | Bildstein, Benno | |
| dc.date.accessioned | 2019-01-07T13:32:15Z | |
| dc.date.available | 2019-01-07T13:32:15Z | |
| dc.date.issued | 2019-03-25 | |
| dc.description.abstract | Thermal or photochemical metal-centered cycloaddition reactions of azidocobaltocenium hexafluoridophosphate or azidoferrocene with (cyclooctadiene)(cyclopentadienyl)cobalt(I) afforded the first metallocenyl-substituted tetrazene cyclopentadienyl cobalt complexes together with azocobaltocenium or azoferrocene as side products. The trimetallic CpCo compounds are highly conjugated, colored, and redox-active metallo-aromatic compounds, as shown by their spectroscopic, structural, and electrochemical properties. The CpCo-tetrazenido complex with two terminally appended cobaltocene units catalyzes electrochemical proton reduction from acetic acid at a mild overpotential (0.35 V). Replacing cobaltocene with ferrocene moieties rendered the complex inactive toward catalysis. | eng |
| dc.description.version | published | eng |
| dc.identifier.doi | 10.1021/acs.organomet.8b00681 | eng |
| dc.identifier.ppn | 1663335095 | |
| dc.identifier.uri | https://kops.uni-konstanz.de/handle/123456789/44423 | |
| dc.language.iso | eng | eng |
| dc.rights | terms-of-use | |
| dc.rights.uri | https://rightsstatements.org/page/InC/1.0/ | |
| dc.subject.ddc | 540 | eng |
| dc.title | Redox-Rich Metallocene Tetrazene Complexes : Synthesis, Structure, Electrochemistry, and Catalysis | eng |
| dc.type | JOURNAL_ARTICLE | eng |
| dspace.entity.type | Publication | |
| kops.citation.bibtex | @article{Vanicek2019-03-25Redox-44423,
year={2019},
doi={10.1021/acs.organomet.8b00681},
title={Redox-Rich Metallocene Tetrazene Complexes : Synthesis, Structure, Electrochemistry, and Catalysis},
number={6},
volume={38},
issn={0276-7333},
journal={Organometallics},
pages={1361--1371},
author={Vanicek, Stefan and Jochriem, Markus and Hassenrück, Christopher and Roy, Souvik and Kopacka, Holger and Wurst, Klaus and Müller, Thomas and Winter, Rainer F. and Reisner, Erwin and Bildstein, Benno}
} | |
| kops.citation.iso690 | VANICEK, Stefan, Markus JOCHRIEM, Christopher HASSENRÜCK, Souvik ROY, Holger KOPACKA, Klaus WURST, Thomas MÜLLER, Rainer F. WINTER, Erwin REISNER, Benno BILDSTEIN, 2019. Redox-Rich Metallocene Tetrazene Complexes : Synthesis, Structure, Electrochemistry, and Catalysis. In: Organometallics. 2019, 38(6), pp. 1361-1371. ISSN 0276-7333. eISSN 1520-6041. Available under: doi: 10.1021/acs.organomet.8b00681 | deu |
| kops.citation.iso690 | VANICEK, Stefan, Markus JOCHRIEM, Christopher HASSENRÜCK, Souvik ROY, Holger KOPACKA, Klaus WURST, Thomas MÜLLER, Rainer F. WINTER, Erwin REISNER, Benno BILDSTEIN, 2019. Redox-Rich Metallocene Tetrazene Complexes : Synthesis, Structure, Electrochemistry, and Catalysis. In: Organometallics. 2019, 38(6), pp. 1361-1371. ISSN 0276-7333. eISSN 1520-6041. Available under: doi: 10.1021/acs.organomet.8b00681 | eng |
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<dcterms:abstract xml:lang="eng">Thermal or photochemical metal-centered cycloaddition reactions of azidocobaltocenium hexafluoridophosphate or azidoferrocene with (cyclooctadiene)(cyclopentadienyl)cobalt(I) afforded the first metallocenyl-substituted tetrazene cyclopentadienyl cobalt complexes together with azocobaltocenium or azoferrocene as side products. The trimetallic CpCo compounds are highly conjugated, colored, and redox-active metallo-aromatic compounds, as shown by their spectroscopic, structural, and electrochemical properties. The CpCo-tetrazenido complex with two terminally appended cobaltocene units catalyzes electrochemical proton reduction from acetic acid at a mild overpotential (0.35 V). Replacing cobaltocene with ferrocene moieties rendered the complex inactive toward catalysis.</dcterms:abstract>
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