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Volumn 5, Issue 21, 2003, Pages 3911-3914

Selective Fluorescence Quenching of 2,3-Diazabicyclo[2.2.2]oct-2-ene by Nucleotides

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE; CYTIDINE; DEUTERIUM; DOUBLE STRANDED DNA; FLUORESCENT DYE; GUANOSINE; HYDROGEN; ISOTOPE; NUCLEOTIDE; THYMIDINE; URIDINE;

EID: 0242459944     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol035454q     Document Type: Article
Times cited : (48)

References (51)
  • 20
    • 0242510352 scopus 로고    scopus 로고
    • note
    • 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.
  • 26
    • 0033569373 scopus 로고    scopus 로고
    • 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.
    • (1999) Phys. Chem. Chem. Phys , vol.1 , pp. 4827-4831
    • Anderson, R.F.1    Wright, G.A.2
  • 27
    • 29544444893 scopus 로고
    • 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.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 6406-6407
    • Saito, I.1    Takayama, M.2    Sugiyama, H.3    Nakatani, K.4    Tsuchida, A.5    Yamamoto, M.6
  • 28
    • 0035140955 scopus 로고    scopus 로고
    • 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.
    • (2001) Anal. Sci. , vol.17 , pp. 155-160
    • Torimura, M.1    Kurata, S.2    Yamada, K.3    Yokomaku, T.4    Kamagata, Y.5    Kanagawa, T.6    Kurane, R.7
  • 40
    • 0016150491 scopus 로고
    • 1H NMR experiments demonstrated that this rate is not enhanced in the presence of DBO (this work).
    • 1H NMR experiments demonstrated that this rate is not enhanced in the presence of DBO (this work).
    • (1974) Proc. Natl. Acad. Sci. U.S.A. , vol.71 , pp. 1356-1360
    • Gamble, R.C.1    Schimmel, P.R.2
  • 43
    • 0242595081 scopus 로고    scopus 로고
    • note
    • Calculations were performed within Hyperchem 6.01 (Hypercube, Inc., Gainesville, FL).
  • 48
    • 0000995482 scopus 로고    scopus 로고
    • Vögtle, F., Ed.; Elsevier Press: New York
    • (b) Mock, W. L. In Comprehensive Supramolecular Chemistry; Vögtle, F., Ed.; Elsevier Press: New York, 1997; Vol. 2, pp 477-493.
    • (1997) Comprehensive Supramolecular Chemistry , vol.2 , pp. 477-493
    • Mock, W.L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.