Maeda, Y., et al. “A Nonspectroscopic Method to Determine the Photolytic Decomposition Pathways of 3-Chloro-3-Alkyldiazirine: Carbene, Diazo and Rearrangement in Excited State”. Journal of the American Chemical Society, vol. 124, no. 32, 2002, pp. 9465-8, https://doi.org/10.1021/ja0116876.

Genre

  • Journal Article
Contributors
Author: Maeda, Y.
Author: Kato, T.
Author: Liu, Michael T. H.
Author: Nagase, S.
Author: Akasaka, T.
Author: Niino, Y.
Author: Kobayashi, K.
Author: Wakahara, T.
Date Issued
2002
Abstract

C-60 acts as a mechanistic probe for the formation of carbene, diazo compound, and for the rearranged product via the excited state in the photolysis of 3-chloro-3-isopropyldiazirine and 3-chloro-3-chloromethyldiazirine. The carbene adds to C-60 to form methanofullerene, whereas the diazo compound adds to C-60 to form fulleroid. The olefin product arises as a result of the rearrangement in the excited state.

Note

Univ Tsukuba, Ctr Tsukuba Adv Res Alliance, Tsukuba, Ibaraki 3058577, Japan. Niigata Univ, Grad Sch Sci & Technol, Niigata 9502181, Japan. Univ Prince Edward Isl, Dept Chem, Charlottetown, PE C1A 4P3, Canada. Inst Mol Sci, Dept Theoret Studies, (TRUNCATED)

WASHINGTON; 1155 16TH ST, NW, WASHINGTON, DC 20036 USA

AMER CHEMICAL SOC

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Source type: Electronic(1)

Language

  • English

Subjects

  • EXCHANGE
  • HYDROGEN MIGRATION
  • ALKYLCHLOROCARBENES
  • Chemistry, Multidisciplinary
  • DIAZIRINES
  • C-60
Page range
9465-9468
Host Title
Journal of the American Chemical Society
Host Abbreviated Title
J.Am.Chem.Soc.
Volume
124
Issue
32
ISSN
0002-7863

Department