Angewandte Chemie

1999

DOI: 10.1002/(sici)1521-3757(19990816)111:16<2504::aid-ange2504>3.0.co;2-i

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Auf dem Weg zur vollständigen Kontrolle der sechsfachen Funktionalisierung von Buckminsterfulleren (C60) an oktaedrischen Positionen

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Cited by 13 publications

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A Parallel Library of all Seven A2+B2+C2Th Regioisomeric Hexakisadducts of Fullerene C60: Inspiration from Werner's Octahedral Stereoisomerism

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2000

Angewandte Chemie

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Drei Substituentenpaare können nacheinander an C60 addiert werden, wobei hochregioselektiv Verbindungen (1 a und 1 b) mit ähnlicher räumlicher Verteilung der Substituenten, aber unterschiedlichen Kante‐zu‐Fläche‐Beziehungen erhalten werden. Die Strukturen dieser Isomere können dank der durch die magnetisch anisotropen 4,5‐Diazafluoreneinheiten verursachten Änderungen der chemischen Verschiebungen aus den NMR‐Spektren abgeleitet werden.

A Parallel Library of all Seven A2+B2+C2Th Regioisomeric Hexakisadducts of Fullerene C60: Inspiration from Werner's Octahedral Stereoisomerism

¹

,

²

2000

Angewandte Chemie

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Drei Substituentenpaare können nacheinander an C60 addiert werden, wobei hochregioselektiv Verbindungen (1 a und 1 b) mit ähnlicher räumlicher Verteilung der Substituenten, aber unterschiedlichen Kante‐zu‐Fläche‐Beziehungen erhalten werden. Die Strukturen dieser Isomere können dank der durch die magnetisch anisotropen 4,5‐Diazafluoreneinheiten verursachten Änderungen der chemischen Verschiebungen aus den NMR‐Spektren abgeleitet werden.

Th-Symmetrical Hexakisadducts of C60 with a Densely Packed π-Donor Shell Can Act as Energy- or Electron-Transducing Systems

Luo²,

et al. 2002

Chem. Eur. J.

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A Parallel Library of all Seven A2+B2+C2Th Regioisomeric Hexakisadducts of Fullerene C60: Inspiration from Werner's Octahedral Stereoisomerism

¹

,

²

2000

Angew. Chem. Int. Ed.

Self Cite

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No abstract

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