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Volumn 4, Issue 17, 2002, Pages 2901-2904

Calix[4]arene-functionalized naphthalene and perylene imide dyes

Author keywords

[No Author keywords available]

Indexed keywords

CALIX(4)ARENE; CALIXARENE; COLORING AGENT; FLUORESCENT DYE; IMIDE; NAPHTHALENE; NAPHTHALENE DERIVATIVE; PERYLENE; PHENOL DERIVATIVE;

EID: 19044371733     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol026402o     Document Type: Article
Times cited : (30)

References (32)
  • 6
    • 0002045307 scopus 로고    scopus 로고
    • Double- and multi-calixarenes
    • Asfari, Z., Böhmer, V., Harrowfield, J., Vicens, J., Eds.; Kluwer: Dordrecht, The Netherlands, Chapter 7
    • See: Saadioui, M.; Böhmer, V. Double- and Multi-Calixarenes. In Calixarenes 2001; Asfari, Z., Böhmer, V., Harrowfield, J., Vicens, J., Eds.; Kluwer: Dordrecht, The Netherlands, 2001; Chapter 7, pp 130-154.
    • (2001) Calixarenes 2001 , pp. 130-154
    • Saadioui, M.1    Böhmer, V.2
  • 10
    • 0002889190 scopus 로고    scopus 로고
    • Coordination chemistry and catalysis
    • Asfari, Z., Böhmer, V., Harrowfield, J., Vicens, J., Eds.; Kluwer: Dordrecht, The Netherlands, Chapter 28
    • (a) Steyer, S.; Jeunesse, C.; Armspach, D.; Matt, D.; Harrowfield, J. Coordination Chemistry and Catalysis. In Calixarenes 2001; Asfari, Z., Böhmer, V., Harrowfield, J., Vicens, J., Eds.; Kluwer: Dordrecht, The Netherlands, 2001; Chapter 28, pp 513-535.
    • (2001) Calixarenes 2001 , pp. 513-535
    • Steyer, S.1    Jeunesse, C.2    Armspach, D.3    Matt, D.4    Harrowfield, J.5
  • 12
    • 0037192455 scopus 로고    scopus 로고
    • General articles on self-assembly: (a) Lehn, J.-M. Science 2002, 295, 2400-2403.
    • (2002) Science , vol.295 , pp. 2400-2403
    • Lehn, J.-M.1
  • 26
  • 28
    • 84872275541 scopus 로고    scopus 로고
    • note
    • -3, respectively.
  • 29
    • 0003942864 scopus 로고
    • Wiley & Sons: New York
    • For other examples of "crystallization-induced asymmetric transformation" of racemates, see: Stereochemistry of Organic Compounds; Eliel, E. L., Wilen, S. H., Eds.; Wiley & Sons: New York, 1994; pp 316-317.
    • (1994) Stereochemistry of Organic Compounds , pp. 316-317
    • Eliel, E.L.1    Wilen, S.H.2
  • 30
    • 84872274926 scopus 로고    scopus 로고
    • note
    • 3, 400 MHz, 25 °C) spectra. 4: 8.60 (d, J = 7.4 Hz, 2H), 8.24 (d, J = 8.2 Hz, 2H), 7.82 (t, J = 7.8 Hz, 2H), 7.05 (s, 2H), 6.99 (s, 2H), 6.57 (s, 4H), 4.46 and 3.14 (AB two d, J = 12.9 Hz, 4H), 4.43 and 3.13 (AB two d, J = 12.9 Hz, 4H), 4.13 (t, J = 8.6 Hz, 2H), 4.01 (t, J = 8.2 Hz, 2H), 3.71 (t, J = 7.4 Hz, 4H), 2.14 (m, 4H), 1.92 (m, 4H), 1.50-1.20 (m, 16H), 1.29 (s, 9H), 0.95 (t, J = 7.0 Hz, 12H), 0.93 (s, 18H). 5: 8.44 (d, J = 7.2 Hz, 4H), 8.15 (d, J = 8.1 Hz, 4H), 7.68 (t, J = 7.6 Hz, 4H), 6.90 and 6.80 (AB two d, J = 2.0 Hz, 4H), 6.88 and 6.73 (AB two d, J = 2.4 Hz, 4H), 4.54 and 3.25 (AB two d, J = 13.3 Hz, 2H), 4.52 and 3.21 (AB two d, J = 12.7 Hz, 2H), 4.51 and 3.21 (AB two d, J = 12.7 Hz, 4H), 3.96 (m, 4H), 3.88 (m, 4H), 2.15-1.95 (m, 8H), 1.21 s (18H), 1.04 (t, J = 7.2 Hz, 6H), 1.02 (t, J = 7.3 Hz, 6H). 6: 8.70-6.30 (br s, 12H), 6.82 (s, 4H), 6.78 (s, 4H), 4.51 and 3.19 (AB two d, J = 12.8 Hz, 8H), 4.01 (t, J = 7.3 Hz, 4H), 3.89 (t, J = 7.3 Hz, 4H), 2.25-1.85 (m, 8H), 1.50-1.30 (m, 16H), 1.09 (s, 18H), 0.99 (t, J = 7.0 Hz, 6H), 0.94 (t, J = 7.0 Hz, 6H). 7a: 8.72 and 8.67 (AB two d, 8H, J = 8.0 Hz), 7.05 (s, 4H), 7.02 (s, 4H), 6.60 (s, 8H), 4.49 and 3.17 (AB two d, J = 12.7 Hz, 8H), 4.45 and 3.15 (AB two d, J = 12.5 Hz, 8H), 4.15 (t, J = 8.2 Hz, 4H), 4.01 (t, J = 8.3 Hz, 4H), 3.74 (t, J = 6.8 Hz, 8H), 2.15 (q, J = 7.8 Hz, 4H), 2.13 (q, J = 7.8 Hz, 4H), 1.94 (q, J = 7.3 Hz, 8H), 1.45-1.20 (m, 32H), 1.29 (s, 18H), 0.99 (t, J = 7.0 Hz, 24H), 0.96 (s, 36H), 7b: 8.14 (s, 4H), 7.23 and 6.85 (AB two d, J = 8.7 Hz, 16H), 6.86 (s, 4H), 6.79 (s, 4H), 6.65 and 6.60 (AB two d, J = 1.7 Hz, 8H), 4.43 and 3.11 (AB two d, J = 12.4 Hz, 8H), 4.40 and 3.11 (AB two d, J = 12.4 Hz, 8H), 4.00 (t, J = 7.8 Hz, 4H), 3.91 (t, J = 8.2 Hz, 4H), 3.77 (m, 8H), 2.04 (m, 8H), 1.95 (m, 8H), 1.45-1.35 (m, 32H), 1.27 (s, 36H), 1.08 (s, 18H), 0.96 (t, J = 7.0 Hz, 24H), 0.93 (s, 36H).


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