ChemInform Abstract: Chemo-, Regio- and Stereoselective Tricyclohexylphosphine-Catalyzed [3 + 2] Cycloaddition of Enynes with [60]Fullerene Initiated by 1,4-Michael Addition: Synthesis of Cyclopenteno[60]fullerenes and Their Electrochemical Properties

ChemInform Abstract: Chemo-, Regio- and Stereoselective Tricyclohexylphosphine-Catalyzed [3 + 2] Cycloaddition of Enynes with [60]Fullerene Initiated by 1,4-Michael Addition: Synthesis of Cyclopenteno[60]fullerenes and Their Electrochemical Properties

The target compounds exhibit comparable or higher LUMO energy levels than a typical n‐type material, [6,6]‐phenyl‐C61‐butyric acid methyl ester.

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Veröffentlicht in:ChemInform 2013-12, Vol.44 (51), p.no-no
Hauptverfasser: Tseng, Po-Yen, Chuang, Shih-Ching
Format: Artikel
Sprache:eng
Schlagworte:
Analytical chemistry
cycloaddition reactions
fullerene derivatives
optical properties (excluding spectra) (organic substances)
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Zusammenfassung:The target compounds exhibit comparable or higher LUMO energy levels than a typical n‐type material, [6,6]‐phenyl‐C61‐butyric acid methyl ester.
ISSN:0931-7597
1522-2667
DOI:10.1002/chin.201351112