Redox-active Diazaphenalenyl-based Molecule and Neutral Radical Formation
A redox-active molecule, 2,5,8-tri(4-pyridyl)-1,3-diazaphenalene (TPDAP), was synthesized by four-step reactions. The two-step redox reaction was revealed by solid-state cyclic voltammetry. The crystal was obtained by sublimation under reduced pressure and characterized by single-crystal X-ray struc...
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Veröffentlicht in: | Chemistry letters 2015-08, Vol.44 (8), p.1131-1133 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | A redox-active molecule, 2,5,8-tri(4-pyridyl)-1,3-diazaphenalene (TPDAP), was synthesized by four-step reactions. The two-step redox reaction was revealed by solid-state cyclic voltammetry. The crystal was obtained by sublimation under reduced pressure and characterized by single-crystal X-ray structure determination. Oxidation of TPDAP produced a neutral radical that was characterized by ESR. |
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ISSN: | 0366-7022 1348-0715 |
DOI: | 10.1246/cl.150410 |