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2
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0031191655
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For a leading review, see
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(c) The pyrene exciplex formation is another remarkable mechanism. Yamauchi, A.; Hayashita, T.; Nishizawa, S.; Watanabe, M.; Teramae, N. J. Am. Chem. Soc. 1999, 121, 2319-2320.
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A is the molar absorption coefficient of the acceptor. The pair of chromophores meets the basic requirement for FRET: the donor emission band strongly overlaps the acceptor absorption band. Gilat, S. L.; Adronov, A.; Fréchet, J. M. J. Angew. Chem. Int. Ed. 1999, 38, 1422-1427.
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A is the molar absorption coefficient of the acceptor. The pair of chromophores meets the basic requirement for FRET: the donor emission band strongly overlaps the acceptor absorption band. Gilat, S. L.; Adronov, A.; Fréchet, J. M. J. Angew. Chem. Int. Ed. 1999, 38, 1422-1427.
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14
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34547465886
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2, ΔFI = 4) means that the intermolecular quenching effect can be ruled out at the experimental concentration (∼1 μM).
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2, ΔFI = 4) means that the intermolecular quenching effect can be ruled out at the experimental concentration (∼1 μM).
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15
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34547425564
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-1) = 322, 4000; 1,8-naphthalic anhydride: 327, 14000; methyl red: 410, 23000.
-
-1) = 322, 4000; 1,8-naphthalic anhydride: 327, 14000; methyl red: 410, 23000.
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-
-
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20
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12344276959
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