Functionalization of [60]fullerene and of [60]fullerene monoadducts by photochemical cycloaddition of 4-methyl-1,2,4-triazoline-3,5-dione
Ulmer L, Siedschlag C, Mattay J (2003)
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2003(19): 3811-3817.
Zeitschriftenaufsatz
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Autor*in
Ulmer, L;
Siedschlag, C;
Mattay, JochenUniBi
Abstract / Bemerkung
The photoreactions of 4-methyl-1,2,4-triazoline-3,5-dione (NMTAD) with C-60 and with several fullerene derivatives have been studied. In general, NMTAD cycloadds to C-60 and to its monoadducts with closed structures in a highly regioselective [2+2] fashion at a cis-1 [6,6] double bond. Cycloadditions to azafulleroids occur by a slightly different pathway and result in partially cluster-opened bis(adducts). 1,6-Methano[60]fulleroid, however, also undergoes a [2+2+2] cycloaddition in the absence of light. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003).
Stichworte
bisfunctionalization;
photochemical cycloaddition;
[60]fullerene
Erscheinungsjahr
2003
Zeitschriftentitel
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Band
2003
Ausgabe
19
Seite(n)
3811-3817
ISSN
1434-193X
eISSN
1099-0690
Page URI
https://pub.uni-bielefeld.de/record/1609994
Zitieren
Ulmer L, Siedschlag C, Mattay J. Functionalization of [60]fullerene and of [60]fullerene monoadducts by photochemical cycloaddition of 4-methyl-1,2,4-triazoline-3,5-dione. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY. 2003;2003(19):3811-3817.
Ulmer, L., Siedschlag, C., & Mattay, J. (2003). Functionalization of [60]fullerene and of [60]fullerene monoadducts by photochemical cycloaddition of 4-methyl-1,2,4-triazoline-3,5-dione. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2003(19), 3811-3817. https://doi.org/10.1002/ejoc.200300297
Ulmer, L, Siedschlag, C, and Mattay, Jochen. 2003. “Functionalization of [60]fullerene and of [60]fullerene monoadducts by photochemical cycloaddition of 4-methyl-1,2,4-triazoline-3,5-dione”. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2003 (19): 3811-3817.
Ulmer, L., Siedschlag, C., and Mattay, J. (2003). Functionalization of [60]fullerene and of [60]fullerene monoadducts by photochemical cycloaddition of 4-methyl-1,2,4-triazoline-3,5-dione. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2003, 3811-3817.
Ulmer, L., Siedschlag, C., & Mattay, J., 2003. Functionalization of [60]fullerene and of [60]fullerene monoadducts by photochemical cycloaddition of 4-methyl-1,2,4-triazoline-3,5-dione. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2003(19), p 3811-3817.
L. Ulmer, C. Siedschlag, and J. Mattay, “Functionalization of [60]fullerene and of [60]fullerene monoadducts by photochemical cycloaddition of 4-methyl-1,2,4-triazoline-3,5-dione”, EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, vol. 2003, 2003, pp. 3811-3817.
Ulmer, L., Siedschlag, C., Mattay, J.: Functionalization of [60]fullerene and of [60]fullerene monoadducts by photochemical cycloaddition of 4-methyl-1,2,4-triazoline-3,5-dione. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY. 2003, 3811-3817 (2003).
Ulmer, L, Siedschlag, C, and Mattay, Jochen. “Functionalization of [60]fullerene and of [60]fullerene monoadducts by photochemical cycloaddition of 4-methyl-1,2,4-triazoline-3,5-dione”. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2003.19 (2003): 3811-3817.
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