Reaction of [60]fullerene with morpholine and piperidine: Preferred 1,4-additions and fullerene dimer formation

Schick G, Kampe KD, Hirsch A (1995)


Publication Type: Journal article, Original article

Publication year: 1995

Journal

Original Authors: Schick G., Kampe K.-D., Hirsch A.

Publisher: Royal Society of Chemistry

Pages Range: 2023-2024

Journal Issue: 19

DOI: 10.1039/C39950002023

Abstract

Reactions of an excess of secondary amines with benzene solutions of [60]fullerene in the presence of oxygen lead to dehydrogenated bisadducts and tetraadduct epoxides with a defined 1,4-addition pattern of the amino groups as well as to the first example of an aminated fullerene dimer.

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How to cite

APA:

Schick, G., Kampe, K.-D., & Hirsch, A. (1995). Reaction of [60]fullerene with morpholine and piperidine: Preferred 1,4-additions and fullerene dimer formation. Journal of the Chemical Society - Series Chemical Communications, 19, 2023-2024. https://doi.org/10.1039/C39950002023

MLA:

Schick, Georg, Klaus-Dieter Kampe, and Andreas Hirsch. "Reaction of [60]fullerene with morpholine and piperidine: Preferred 1,4-additions and fullerene dimer formation." Journal of the Chemical Society - Series Chemical Communications 19 (1995): 2023-2024.

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