Supramolecular electro- and proto-photoswitch

Chemistry Letters

Volumn , Issue 3, 1999, Pages 269-270

  Otsuki, Joe ^a   Harada, Kenkichi ^a   Araki, Koji ^a  

^a INSTITUTE OF INDUSTRIAL SCIENCE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0033246952     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.1999.269     Document Type: Article

References (19)

1. J. Otsuki, K. Sato, M. Tsujino, N. Okuda, K. Araki, and M. Seno, Chem. Lett., 1996, 847; J. Otuski, M. Tsujino, T. Iizaki, K. Araki, M. Seno, K. Takatera, and T. Watanabe, J. Am. Chem. Soc., 119, 7895 (1997).
2. J. Otsuki, K. Sato, M. Tsujino, N. Okuda, K. Araki, and M. Seno, Chem. Lett., 1996, 847; J. Otuski, M. Tsujino, T. Iizaki, K. Araki, M. Seno, K. Takatera, and T. Watanabe, J. Am. Chem. Soc., 119, 7895 (1997).
3. J.-M. Lehn, "Supramolecular Chemistry," VCH, Weinheim (1995); V. Goulle, A. Harriman, and J. M. Lehn, J. Chem. Soc., Chem. Commun., 1993, 1034.
4. J.-M. Lehn, "Supramolecular Chemistry," VCH, Weinheim (1995); V. Goulle, A. Harriman, and J. M. Lehn, J. Chem. Soc., Chem. Commun., 1993, 1034.
5. L. Fabbrizzi and A. Poggi, Chem. Soc. Rev., 1995, 197; G. De Santis, L. Fabbrizzi, M. Licchelli, C. Mangano, and D. Sacchi, Inorg. Chem., 34, 3581 (1995).
6. L. Fabbrizzi and A. Poggi, Chem. Soc. Rev., 1995, 197; G. De Santis, L. Fabbrizzi, M. Licchelli, C. Mangano, and D. Sacchi, Inorg. Chem., 34, 3581 (1995).
7. A. P. de Silva, H. Q. N. Gunaratne, T. Gunnlaugsson, A. J. M. Huxley, C. P. McCoy, J. T. Rademacher, and T. E. Rice, Chem. Rev., 97, 1515 (1997).
8. T. Hayashi and H. Ogoshi, Chem. Soc. Rev., 26, 355 (1997).
9. M. D. Ward, Chem. Soc. Rev., 26, 365 (1997).
10. M. Seno, K. Araki, and J. Otsuki, "Chobunshi Kagaku (Supramolecular Chemistry)," Tokyo Kagaku Dojin, Tokyo (1998).
11. R. J. Abraham, G. R. Bedford, D. McNeillie, and B. Wright, Org. Magn. Reson., 14, 418 (1980).
12. J. Otsuki, K. Harada, K. Toyama, Y. Hirose, K. Araki, M. Seno, K. Takatera, and T. Watanabe, Chem. Commun., 1998, 1515.
13. +) is more negative than that of PhNNPy (-1.84 V).
14. + and Pt, respectively. The potential was applied until no more spectroscopic change was observed. Completion of the redox reaction was difficult due to the bulk nature of the cell.
15. Y. Iseki, E. Watanebe, A. Mori, and S. Inoue, J. Am. Chem. Soc., 115, 7313 (1993); Y. Iseki and S. Inoue, J. Chem. Soc., Chem. Commun., 1994, 2577.
16. Y. Iseki, E. Watanebe, A. Mori, and S. Inoue, J. Am. Chem. Soc., 115, 7313 (1993); Y. Iseki and S. Inoue, J. Chem. Soc., Chem. Commun., 1994, 2577.
17. K.-S. Cheon, R. A. Cox, S-R. Keum, and E. Buncel, J. Chem. Soc., Perkin Trans. 2, 1998, 1231.
18. The acid and base do not have any direct effect on ZnTPP or its fluorescence, except that prolonged exposure to acid causes demetallation of ZnTPP.
19. The effect of cis-trans isomerization of PhNNPy was also investigated. However, no indication was obtained concerning changes either in coordination or quenching behaviour concomitant with the isomerization reaction.