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Volumn 37, Issue 13-14, 1998, Pages 1913-1916

Self-assembling supramolecular daisy chains

Author keywords

Crown compounds; Molecular recognition; Noncovalent interactions; Supramolecular chemistry

Indexed keywords


EID: 0032479772     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(19980803)37:13/14<1913::AID-ANIE1913>3.0.CO;2-W     Document Type: Article
Times cited : (123)

References (39)
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    • For examples of intramolecular complexes formed by the insertion of the "tail" of a molecule through the cavity of its own "head", see a) S. Shinkai, M. Ishihara, K. Ueada, J. Chem. Soc. Perkin Trans. 2 1995, 511-518; b) R. Corradini, A. Dossena, R. Marchelli, A. Panagia, G. Sartor, M. Saviano, A. Lombardi, V. Pavone, Chem. Eur. J. 1996, 6, 373-381; c) P. R. Ashton, R. Ballardini, V. Balzani, S. E. Boyd, A. Credi, M. T. Gandolfi, M. Gómez-López, S. Iqbal, D. Philp, J. A. Preece, L. Prodi, H. G. Ricketts, J. F. Stoddart, M. S. Tolley, M. Venturi, A. J. P. White, D. J. Williams, ibid. 1997, 3, 152-170.
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    • For examples of intramolecular complexes formed by the insertion of the "tail" of a molecule through the cavity of its own "head", see a) S. Shinkai, M. Ishihara, K. Ueada, J. Chem. Soc. Perkin Trans. 2 1995, 511-518; b) R. Corradini, A. Dossena, R. Marchelli, A. Panagia, G. Sartor, M. Saviano, A. Lombardi, V. Pavone, Chem. Eur. J. 1996, 6, 373-381; c) P. R. Ashton, R. Ballardini, V. Balzani, S. E. Boyd, A. Credi, M. T. Gandolfi, M. Gómez-López, S. Iqbal, D. Philp, J. A. Preece, L. Prodi, H. G. Ricketts, J. F. Stoddart, M. S. Tolley, M. Venturi, A. J. P. White, D. J. Williams, ibid. 1997, 3, 152-170.
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    • note
    • -2M): δ = 165.5, 155.0, 151.0, 150.0, 146.5, 146.4, 134.7, 133.5, 132.7, 131.2, 131.1, 130.6, 130.4, 129.2, 127.8, 127.8, 127.2, 126.5, 123.0, 71.4, 70.4, 70.4, 70.1, 69.1, 65.8, 65.1.
  • 33
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    • note
    • 6 at various concentrations, see the supporting information.
  • 34
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    • note
    • o|), 2θ ≤ 106°) and 496 parameters. Crystallographic data (excluding structure factors) for the structure reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-101 199. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road. Cambridge CB21EZ, UK (fax: (+44) 1223-336-033; e-mail: deposit@ccdc.cam.ac.uk).
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    • +-H⋯ O] and [C-H ⋯ O] hydrogen bonding, see P. R. Ashton, I. Baxter, S. J. Cantrill, M. C. T. Fyfe, P. T. Glink, J. F. Stoddart, A. J. P. White, D. J. Williams, Angew. Chem. 1998, 110, 1344-1347; Angew. Chem. Int. Ed. 1998, 37, 1294-1297.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 1294-1297
  • 38
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    • note
    • 6O axis of the 1,5-dioxynaphthalene ring system.
  • 39
    • 0344931378 scopus 로고    scopus 로고
    • note
    • [8] Note that only [c]daisy chains experience maximal (recognition) site occupancy (ref. [2b], p. 182-183) and that small [c]daisy chains (supermolecules) are also favored entropically with respect to large [a]daisy chains (supramolecular arrays).


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