The Most Stable and Fully Characterized Functionalized Heptacene
Identifieur interne : 001018 ( Main/Exploration ); précédent : 001017; suivant : 001019The Most Stable and Fully Characterized Functionalized Heptacene
Auteurs : Doris Chun [États-Unis] ; Yang Cheng [États-Unis] ; Fred Wudl [États-Unis]Source :
- Angewandte Chemie [ 0044-8249 ] ; 2008-10-20.
English descriptors
- KwdEn :
- Absorption spectra, Acene, Acene backbone, Angew, Angewandte chemie, Chem, Cyclic voltammetry, Derivative, Ethyl acetate, Functionalized, Heptacene, Heptacene derivatives, Lumo levels, Metal reduction, Phenyl groups, Reaction mixture, Small molecules, Solid line, Solid state, Tips groups, Toluene, Verlag gmbh, Version bruker, Vibronic pattern, Weinheim angew.
- Teeft :
- Absorption spectra, Acene, Acene backbone, Angew, Angewandte chemie, Chem, Cyclic voltammetry, Derivative, Ethyl acetate, Functionalized, Heptacene, Heptacene derivatives, Lumo levels, Metal reduction, Phenyl groups, Reaction mixture, Small molecules, Solid line, Solid state, Tips groups, Toluene, Verlag gmbh, Version bruker, Vibronic pattern, Weinheim angew.
Abstract
Sieben gewinnt: Kristalle eines Heptacens mit Phenyl‐ und Triisopropylsilylethinyl‐Substituenten (siehe Schema) lassen sich in Mineralöl mindestens 21 Tage lagern und sind 24 h in einer entgasten Lösung stabil. Die richtige Kombination funktioneller Gruppen macht diese Verbindung mit sieben linear kondensierten Benzolringen zum bislang stabilsten Heptacenderivat.
Url:
DOI: 10.1002/ange.200803345
Affiliations:
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Le document en format XML
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<front><div type="abstract">Sieben gewinnt: Kristalle eines Heptacens mit Phenyl‐ und Triisopropylsilylethinyl‐Substituenten (siehe Schema) lassen sich in Mineralöl mindestens 21 Tage lagern und sind 24 h in einer entgasten Lösung stabil. Die richtige Kombination funktioneller Gruppen macht diese Verbindung mit sieben linear kondensierten Benzolringen zum bislang stabilsten Heptacenderivat.</div>
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