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Volumn 69, Issue 23, 2004, Pages 8086-8092

Synthesis and electrogenerated chemiluminescence of donor-substituted phenylethynylcoumarins

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL BONDS; CHEMILUMINESCENCE; COMPOSITION; ELECTRON ABSORPTION; ION SOURCES; SYNTHESIS (CHEMICAL);

EID: 8644282726     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0493424     Document Type: Article
Times cited : (64)

References (49)
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    • Iodosalicylaldehyde was prepared according to: Klein, S. I.; Guertin, K. R.; Spada, A. P.; Pauls, H. W.; Gong, Y.; McGarry, D. G. U.S. patent, 2001, 6323227. 4-Iodosalicylaldehyde was cyclized with acetic anhydride to obtain 7-iodocoumarin in 40% yield according to: Furniss, B. S.; Hannaford, A. J.; Smith, P. W. G.; Tatchell, A. R. Vogel's Textbook of Practical Organic Chemistry; Wiley: New York, 1989; p 1040.
    • Klein, S.I.1    Guertin, K.R.2    Spada, A.P.3    Pauls, H.W.4    Gong, Y.5    McGarry, D.G.6
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    • Wiley: New York
    • Iodosalicylaldehyde was prepared according to: Klein, S. I.; Guertin, K. R.; Spada, A. P.; Pauls, H. W.; Gong, Y.; McGarry, D. G. U.S. patent, 2001, 6323227. 4-Iodosalicylaldehyde was cyclized with acetic anhydride to obtain 7-iodocoumarin in 40% yield according to: Furniss, B. S.; Hannaford, A. J.; Smith, P. W. G.; Tatchell, A. R. Vogel's Textbook of Practical Organic Chemistry; Wiley: New York, 1989; p 1040.
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    • Furniss, B.S.1    Hannaford, A.J.2    Smith, P.W.G.3    Vogel'S, T.A.R.4
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    • Supporting evidence: When this paper was under review, a paper appeared that postulates the possibility of the annihilation reaction producing excited states other than the photoluminescence state. See: Ketter, J. B.; Wightman, R. M. J. Am. Chem. Soc. 2004, 126, 10183.
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    • Ketter, J.B.1    Wightman, R.M.2
  • 49
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    • Wavefunction, Inc., 18401 Von Karman Ave., Suite 370, Irvine, CA 92612
    • Spartan'04 Windows; Wavefunction, Inc., 18401 Von Karman Ave., Suite 370, Irvine, CA 92612.
    • Spartan'04 Windows


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