Tetra(peri‐naphthylene)anthracene: A Near‐IR Fluorophore with Four‐Stage Amphoteric Redox Properties
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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In: Chemistry – A European Journal 29.6 (2023): e202203101.
- Classification
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Chemie
- Event
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Veröffentlichung
- (where)
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Erlangen
- (who)
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Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
- (when)
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2023
- Creator
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Frisch, Sabine
Neiß, Christian
Lindenthal, Sebastian
Zorn, Nicolas
Rominger, Frank
Görling, Andreas
Zaumseil, Jana
Kivala, Milan
- DOI
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10.1002/chem.202203101
- URN
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urn:nbn:de:bvb:29-opus4-227347
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 11:01 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Frisch, Sabine
- Neiß, Christian
- Lindenthal, Sebastian
- Zorn, Nicolas
- Rominger, Frank
- Görling, Andreas
- Zaumseil, Jana
- Kivala, Milan
- Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
Time of origin
- 2023
Other Objects (12)
Tetra (peri ‐naphthylene) anthracene: A Near‐IR Fluorophore with Four‐Stage Amphoteric Redox Properties
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Anthracene‐Porphyrin Nanoribbons
Über Synthesen methylierter Anthracene
Structural Versatility and Supramolecular Isomerism in Redox-Active Tetra- and Hexaruthenium Macrocycles
Structural Versatility and Supramolecular Isomerism in Redox‐Active Tetra‐ and Hexaruthenium Macrocycles
Nanohoop through Anthracene Photodimerization–Cycloreversion
Anthracene Based Colorimetric Molecular Sensors
Role of Interfacial Potential Drops on Redox‐Couple Dependent Voltages Using Hybridized Si (111)–(Bis) Anthracene Photoelectrodes
Homogene Reaktionsmechanismen elektrochemisch erzeugter Radikalionen substituierter 9-Cyano-anthracene [Cyano-anthracene] in aprotischem Milieu
TETRA-Projekt
Tetra (peri ‐naphthylene) anthracene: A Near‐IR Fluorophore with Four‐Stage Amphoteric Redox Properties
Zur Synthese peri-anellierter Anthracene
Anthracene‐Porphyrin Nanoribbons
Anthracene‐Porphyrin Nanoribbons
Über Synthesen methylierter Anthracene
Structural Versatility and Supramolecular Isomerism in Redox-Active Tetra- and Hexaruthenium Macrocycles
Structural Versatility and Supramolecular Isomerism in Redox‐Active Tetra‐ and Hexaruthenium Macrocycles
Nanohoop through Anthracene Photodimerization–Cycloreversion
Anthracene Based Colorimetric Molecular Sensors
Role of Interfacial Potential Drops on Redox‐Couple Dependent Voltages Using Hybridized Si (111)–(Bis) Anthracene Photoelectrodes
Homogene Reaktionsmechanismen elektrochemisch erzeugter Radikalionen substituierter 9-Cyano-anthracene [Cyano-anthracene] in aprotischem Milieu
TETRA-Projekt
Tetra (peri ‐naphthylene) anthracene: A Near‐IR Fluorophore with Four‐Stage Amphoteric Redox Properties
Zur Synthese peri-anellierter Anthracene
Anthracene‐Porphyrin Nanoribbons
Anthracene‐Porphyrin Nanoribbons
Über Synthesen methylierter Anthracene
Structural Versatility and Supramolecular Isomerism in Redox-Active Tetra- and Hexaruthenium Macrocycles
Structural Versatility and Supramolecular Isomerism in Redox‐Active Tetra‐ and Hexaruthenium Macrocycles
Nanohoop through Anthracene Photodimerization–Cycloreversion
Anthracene Based Colorimetric Molecular Sensors
Role of Interfacial Potential Drops on Redox‐Couple Dependent Voltages Using Hybridized Si (111)–(Bis) Anthracene Photoelectrodes
Homogene Reaktionsmechanismen elektrochemisch erzeugter Radikalionen substituierter 9-Cyano-anthracene [Cyano-anthracene] in aprotischem Milieu