메뉴 건너뛰기




Volumn 121, Issue 26, 1999, Pages 6316-6317

Metal-directed assembly of triple-layered fluorescent metallocyclophanes [6]

Author keywords

[No Author keywords available]

Indexed keywords

FLUORESCENT DYE;

EID: 0033532903     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja991140f     Document Type: Letter
Times cited : (62)

References (30)
  • 4
    • 0003510586 scopus 로고
    • John Wiley & Sons: New York
    • For organic examples, see: (a) Vögtle, F. Cyclophane Chemistry: Synthesis, Structures, and Reactions; John Wiley & Sons: New York, 1993. (b) Ferguson, J. Chem. Rev. 1986, 86, 957-982. (c) Iwama, A.; Toyoda, T.; Yoshida, M.; Otsubo, T.; Sakata, Y.; Misumi, S. Bull. Chem. Soc. Jpn. 1978, 51, 2988-2994. For inorganic examples, see: (d) Slone, R. V.; Benkstein, K. D.; Bélanger, S.; Hupp, J. T.; Guzei, I. A.; Rheingold, A. L. Coord. Chem. Rev. 1998, 171, 221-243. (e) Ashton, P. R.; Balzani, V.; Credi, A.; Kocian, O.; Pasini, D.; Prodi, L.; Spencer, N.; Stoddart, J. F.; Tolley, M. S.; Venturi, M.; White, A. J. P.; Williams, D. J. Chem. Eur. J. 1998, 4, 590-607.
    • (1993) Cyclophane Chemistry: Synthesis, Structures, and Reactions
    • Vögtle, F.1
  • 5
    • 0000282928 scopus 로고
    • For organic examples, see: (a) Vögtle, F. Cyclophane Chemistry: Synthesis, Structures, and Reactions; John Wiley & Sons: New York, 1993. (b) Ferguson, J. Chem. Rev. 1986, 86, 957-982. (c) Iwama, A.; Toyoda, T.; Yoshida, M.; Otsubo, T.; Sakata, Y.; Misumi, S. Bull. Chem. Soc. Jpn. 1978, 51, 2988-2994. For inorganic examples, see: (d) Slone, R. V.; Benkstein, K. D.; Bélanger, S.; Hupp, J. T.; Guzei, I. A.; Rheingold, A. L. Coord. Chem. Rev. 1998, 171, 221-243. (e) Ashton, P. R.; Balzani, V.; Credi, A.; Kocian, O.; Pasini, D.; Prodi, L.; Spencer, N.; Stoddart, J. F.; Tolley, M. S.; Venturi, M.; White, A. J. P.; Williams, D. J. Chem. Eur. J. 1998, 4, 590-607.
    • (1986) Chem. Rev. , vol.86 , pp. 957-982
    • Ferguson, J.1
  • 6
    • 0018241793 scopus 로고
    • For organic examples, see: (a) Vögtle, F. Cyclophane Chemistry: Synthesis, Structures, and Reactions; John Wiley & Sons: New York, 1993. (b) Ferguson, J. Chem. Rev. 1986, 86, 957-982. (c) Iwama, A.; Toyoda, T.; Yoshida, M.; Otsubo, T.; Sakata, Y.; Misumi, S. Bull. Chem. Soc. Jpn. 1978, 51, 2988-2994. For inorganic examples, see: (d) Slone, R. V.; Benkstein, K. D.; Bélanger, S.; Hupp, J. T.; Guzei, I. A.; Rheingold, A. L. Coord. Chem. Rev. 1998, 171, 221-243. (e) Ashton, P. R.; Balzani, V.; Credi, A.; Kocian, O.; Pasini, D.; Prodi, L.; Spencer, N.; Stoddart, J. F.; Tolley, M. S.; Venturi, M.; White, A. J. P.; Williams, D. J. Chem. Eur. J. 1998, 4, 590-607.
    • (1978) Bull. Chem. Soc. Jpn. , vol.51 , pp. 2988-2994
    • Iwama, A.1    Toyoda, T.2    Yoshida, M.3    Otsubo, T.4    Sakata, Y.5    Misumi, S.6
  • 7
    • 0032047384 scopus 로고    scopus 로고
    • For organic examples, see: (a) Vögtle, F. Cyclophane Chemistry: Synthesis, Structures, and Reactions; John Wiley & Sons: New York, 1993. (b) Ferguson, J. Chem. Rev. 1986, 86, 957-982. (c) Iwama, A.; Toyoda, T.; Yoshida, M.; Otsubo, T.; Sakata, Y.; Misumi, S. Bull. Chem. Soc. Jpn. 1978, 51, 2988-2994. For inorganic examples, see: (d) Slone, R. V.; Benkstein, K. D.; Bélanger, S.; Hupp, J. T.; Guzei, I. A.; Rheingold, A. L. Coord. Chem. Rev. 1998, 171, 221-243. (e) Ashton, P. R.; Balzani, V.; Credi, A.; Kocian, O.; Pasini, D.; Prodi, L.; Spencer, N.; Stoddart, J. F.; Tolley, M. S.; Venturi, M.; White, A. J. P.; Williams, D. J. Chem. Eur. J. 1998, 4, 590-607.
    • (1998) Coord. Chem. Rev. , vol.171 , pp. 221-243
    • Slone, R.V.1    Benkstein, K.D.2    Bélanger, S.3    Hupp, J.T.4    Guzei, I.A.5    Rheingold, A.L.6
  • 8
    • 0031804329 scopus 로고    scopus 로고
    • For organic examples, see: (a) Vögtle, F. Cyclophane Chemistry: Synthesis, Structures, and Reactions; John Wiley & Sons: New York, 1993. (b) Ferguson, J. Chem. Rev. 1986, 86, 957-982. (c) Iwama, A.; Toyoda, T.; Yoshida, M.; Otsubo, T.; Sakata, Y.; Misumi, S. Bull. Chem. Soc. Jpn. 1978, 51, 2988-2994. For inorganic examples, see: (d) Slone, R. V.; Benkstein, K. D.; Bélanger, S.; Hupp, J. T.; Guzei, I. A.; Rheingold, A. L. Coord. Chem. Rev. 1998, 171, 221-243. (e) Ashton, P. R.; Balzani, V.; Credi, A.; Kocian, O.; Pasini, D.; Prodi, L.; Spencer, N.; Stoddart, J. F.; Tolley, M. S.; Venturi, M.; White, A. J. P.; Williams, D. J. Chem. Eur. J. 1998, 4, 590-607.
    • (1998) Chem. Eur. J. , vol.4 , pp. 590-607
    • Ashton, P.R.1    Balzani, V.2    Credi, A.3    Kocian, O.4    Pasini, D.5    Prodi, L.6    Spencer, N.7    Stoddart, J.F.8    Tolley, M.S.9    Venturi, M.10    White, A.J.P.11    Williams, D.J.12
  • 22
    • 0344883053 scopus 로고    scopus 로고
    • note
    • 2) = 6.86% for 8635 observed independent reflections (3.54° ≤ 2θ ≤ 48.00°). The asymmetric contains half of the rhodium cation, a tetrafluoroborate anion, three molecules of dichloromethane, and half a molecule of an acetonitrile residing along a 2-fold axis.
  • 27
    • 0344883052 scopus 로고    scopus 로고
    • max = 386 nm(ε = 60 700)
    • max = 386 nm(ε = 60 700).
  • 28
    • 0345314122 scopus 로고    scopus 로고
    • The large decrease in observed fluorescence intensity in 3b is due to "trivial quenching" (quenching due to the reabsorption of emitted light within the sample, not competing decay processes such as energy or electron transfer) as the CT absorption (466 nm) significantly overlaps with the fluorescence emission (442 nm) of the unperturbed anthracene chromophore
    • The large decrease in observed fluorescence intensity in 3b is due to "trivial quenching" (quenching due to the reabsorption of emitted light within the sample, not competing decay processes such as energy or electron transfer) as the CT absorption (466 nm) significantly overlaps with the fluorescence emission (442 nm) of the unperturbed anthracene chromophore.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.