Efficient Diels–Alder Addition of Cyclopentadiene to Lithium Ion Encapsulated [60]Fullerene
Much higher reactivity of [Li+@C60]PF6 – for Diels–Alder cycloaddition toward cyclopentadiene (CpH), in comparison with that of empty C60, was observed. The synthetic method, electrochemical and light absorption properties, and X-ray crystal structure of the product [Li+@C60(CpH)]PF6 – are discussed...
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Veröffentlicht in: | Organic letters 2013-09, Vol.15 (17), p.4466-4469 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Much higher reactivity of [Li+@C60]PF6 – for Diels–Alder cycloaddition toward cyclopentadiene (CpH), in comparison with that of empty C60, was observed. The synthetic method, electrochemical and light absorption properties, and X-ray crystal structure of the product [Li+@C60(CpH)]PF6 – are discussed. |
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ISSN: | 1523-7060 1523-7052 |
DOI: | 10.1021/ol4020046 |