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note
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Note that the acetic acid residue does not contribute to the quenching since sodium acetate (up to 0.2 M) does not cause sizable fluorescence quenching of DBO.
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23
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Note that electron transfer is the most common quenching mechanism for nucleobases: (a) Anderson, R. F.; Wright, G. A. Phys. Chem. Chem. Phys. 1999, 1, 4827-4831. (b) Saito, I.; Takayama, M.; Sugiyama, H.; Nakatani, K.; Tsuchida, A.; Yamamoto, M. J. Am. Chem. Soc. 1995, 117, 6406-6407. (c) Torimura, M.; Kurata, S.; Yamada, K.; Yokomaku, T.; Kamagata, Y.; Kanagawa, T.; Kurane, R. Anal. Sci. 2001, 17, 155-160.
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29544444893
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Note that electron transfer is the most common quenching mechanism for nucleobases: (a) Anderson, R. F.; Wright, G. A. Phys. Chem. Chem. Phys. 1999, 1, 4827-4831. (b) Saito, I.; Takayama, M.; Sugiyama, H.; Nakatani, K.; Tsuchida, A.; Yamamoto, M. J. Am. Chem. Soc. 1995, 117, 6406-6407. (c) Torimura, M.; Kurata, S.; Yamada, K.; Yokomaku, T.; Kamagata, Y.; Kanagawa, T.; Kurane, R. Anal. Sci. 2001, 17, 155-160.
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0035140955
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Note that electron transfer is the most common quenching mechanism for nucleobases: (a) Anderson, R. F.; Wright, G. A. Phys. Chem. Chem. Phys. 1999, 1, 4827-4831. (b) Saito, I.; Takayama, M.; Sugiyama, H.; Nakatani, K.; Tsuchida, A.; Yamamoto, M. J. Am. Chem. Soc. 1995, 117, 6406-6407. (c) Torimura, M.; Kurata, S.; Yamada, K.; Yokomaku, T.; Kamagata, Y.; Kanagawa, T.; Kurane, R. Anal. Sci. 2001, 17, 155-160.
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0016150491
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1H NMR experiments demonstrated that this rate is not enhanced in the presence of DBO (this work).
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1H NMR experiments demonstrated that this rate is not enhanced in the presence of DBO (this work).
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