New effective synthons for supramolecular self-assembly of meso- carboxyphenylporphyrins

Chemical Communications

Volumn , Issue 7, 2000, Pages 585-586

  Diskin Posner, Yael ^a   Dahal, Sanjay ^a   Goldberg, Israel ^a  

^a TEL AVIV UNIVERSITY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

METAL ION; TETRAPHENYLPORPHYRIN DERIVATIVE;

ARTICLE; COMPLEX FORMATION; CRYSTAL; MOLECULAR RECOGNITION; SYNTHESIS;

EID: 0034616197     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b001189o     Document Type: Article

References (15)

1. For recent reviews on noncovalent assembly of porphyrin arrays and their potential applications see: J.-C. Chambron, V. Heitz and J.-P. Sauvage, The Porphyrin Handbook, ed. K. M. Kadish, K. M. Smith and R. Guilard, Academic Press, Orlando FL, 2000, vol. 6, ch. 40; J.-H. Chou, M. E. Kosal, H. S. Nalwa, N. A. Rakow and K. S. Suslick, The Porphyrin Handbook, ed. K. M. Kadish, K. M. Smith and R. Guilard, AP, Orlando FL, 2000, vol. 6, chap. 41.
2. For recent reviews on noncovalent assembly of porphyrin arrays and their potential applications see: J.-C. Chambron, V. Heitz and J.-P. Sauvage, The Porphyrin Handbook, ed. K. M. Kadish, K. M. Smith and R. Guilard, Academic Press, Orlando FL, 2000, vol. 6, ch. 40; J.-H. Chou, M. E. Kosal, H. S. Nalwa, N. A. Rakow and K. S. Suslick, The Porphyrin Handbook, ed. K. M. Kadish, K. M. Smith and R. Guilard, AP, Orlando FL, 2000, vol. 6, chap. 41.
3. P. Dastidar, Z. Stein, I. Goldberg and C. E. Strouse, Supramol. Chem., 1996, 7, 257.
4. Y. Diskin-Posner, R. Krishna Kumar and I. Goldberg, New J. Chem., 1999, 23, 885.
5. Y. Diskin-Posner and I. Goldberg, Chem. Commun., 1999, 1961.
6. Successful tesselation of tetrapyridylporphyrin supramolecular aggregates by transion metal auxiliaries has been reported previously in the solid state (B. F. Abrahams, B. F. Hoskins, D. M. Michail and R. Robson, Nature, 1994, 369, 727), as well as in solution (C. M. Drain and J.-M. Lehn, J. Chem. Soc., Chem. Commun., 1994, 2313; C. M. Drain, F. Nifiatis, A. Vasenko and J. Batteas, Angew. Chem., Int. Ed., 1998, 37, 2344).
7. Successful tesselation of tetrapyridylporphyrin supramolecular aggregates by transion metal auxiliaries has been reported previously in the solid state (B. F. Abrahams, B. F. Hoskins, D. M. Michail and R. Robson, Nature, 1994, 369, 727), as well as in solution (C. M. Drain and J.-M. Lehn, J. Chem. Soc., Chem. Commun., 1994, 2313; C. M. Drain, F. Nifiatis, A. Vasenko and J. Batteas, Angew. Chem., Int. Ed., 1998, 37, 2344).
8. Successful tesselation of tetrapyridylporphyrin supramolecular aggregates by transion metal auxiliaries has been reported previously in the solid state (B. F. Abrahams, B. F. Hoskins, D. M. Michail and R. Robson, Nature, 1994, 369, 727), as well as in solution (C. M. Drain and J.-M. Lehn, J. Chem. Soc., Chem. Commun., 1994, 2313; C. M. Drain, F. Nifiatis, A. Vasenko and J. Batteas, Angew. Chem., Int. Ed., 1998, 37, 2344).
9. O. Ermer, J. Am. Chem. Soc., 1988, 110, 3747.
10. Y. Diskin-Posner, S. Dahal and I. Goldberg, Angew. Chem., Int. Ed., 2000, 39, in press.
11. H.-A. Klok, K. A. Jolliffe, C. L. Schauer, L. J. Prins, J. P. Spatz, M. Möller, P. Timmerman and D. N. Reinhoudt, J. Am. Chem. Soc., 1999, 121, 7154.
12. See, for example: C. M. Drain, S. Gentemann, J. A. Roberts, N. Y. Nelson, C. J. Medforth, S. Jai, M. C. Simpson, K. M. Smith, J. Fajer, J. A. Shelnutt and D. Holten, J. Am. Chem. Soc., 1998, 120, 3781; J. L. Sessler, B. Wang and A. Harriman, J. Am. Chem. Soc., 1995, 117, 704.
13. See, for example: C. M. Drain, S. Gentemann, J. A. Roberts, N. Y. Nelson, C. J. Medforth, S. Jai, M. C. Simpson, K. M. Smith, J. Fajer, J. A. Shelnutt and D. Holten, J. Am. Chem. Soc., 1998, 120, 3781; J. L. Sessler, B. Wang and A. Harriman, J. Am. Chem. Soc., 1995, 117, 704.
14. P. Van der Sluis and A. L. Spek, Acta Crystattogr., Sect. A, 1990, 46, 194; A. L. Spek, Acta Crystallogr., Sect. A, 1990, 46, C34. The 'Squeeze' method referred therein is widely used in crystallographic analysis of compounds containing substantial amounts of disordered solvent which cannot be located precisely from diffraction data.
15. P. Van der Sluis and A. L. Spek, Acta Crystattogr., Sect. A, 1990, 46, 194; A. L. Spek, Acta Crystallogr., Sect. A, 1990, 46, C34. The 'Squeeze' method referred therein is widely used in crystallographic analysis of compounds containing substantial amounts of disordered solvent which cannot be located precisely from diffraction data.