[60]fullerene radical cation: Reactions and mechanism

Siedschlag C, Luftmann H, Wolff C, Mattay J (1999)
TETRAHEDRON 55(25): 7805-7818.

Journal Article | Published | English

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Abstract
C-60 was irradiated in the presence of several electron transfer photosensitizers. Upon addition of H-donors such as N,N-dimethylformamide, 1,3-dioxolane, phenylacetaldehyde, methyl formate, tert-butanol, propionic acid, glycol and methoxyethanol 1-substituted 1,2-dihydro[60]fullerenes 1-3 and 5-11 and in one case a 1,2,3,4-tetrahydro[60]fullerene, 4, were formed. A mechanistic pathway involving C-60(.+) is proposed.
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Siedschlag C, Luftmann H, Wolff C, Mattay J. [60]fullerene radical cation: Reactions and mechanism. TETRAHEDRON. 1999;55(25):7805-7818.
Siedschlag, C., Luftmann, H., Wolff, C., & Mattay, J. (1999). [60]fullerene radical cation: Reactions and mechanism. TETRAHEDRON, 55(25), 7805-7818.
Siedschlag, C., Luftmann, H., Wolff, C., and Mattay, J. (1999). [60]fullerene radical cation: Reactions and mechanism. TETRAHEDRON 55, 7805-7818.
Siedschlag, C., et al., 1999. [60]fullerene radical cation: Reactions and mechanism. TETRAHEDRON, 55(25), p 7805-7818.
C. Siedschlag, et al., “[60]fullerene radical cation: Reactions and mechanism”, TETRAHEDRON, vol. 55, 1999, pp. 7805-7818.
Siedschlag, C., Luftmann, H., Wolff, C., Mattay, J.: [60]fullerene radical cation: Reactions and mechanism. TETRAHEDRON. 55, 7805-7818 (1999).
Siedschlag, C, Luftmann, H, Wolff, C, and Mattay, Jochen. “[60]fullerene radical cation: Reactions and mechanism”. TETRAHEDRON 55.25 (1999): 7805-7818.
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