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Volumn 37, Issue 7, 1998, Pages 975-979

A molecular chameleon: Chromophoric sensing by a self-complexing molecular assembly

Author keywords

Chromophores; Molecular devices; Nanostructures; Receptors; Supramolecular chemistry

Indexed keywords


EID: 0031961088     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(19980420)37:7<975::AID-ANIE975>3.0.CO;2-L     Document Type: Article
Times cited : (40)

References (49)
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    • note
    • 1H NMR time scale at room temperature.
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    • 4+ is a changeable entity, both in terms of its conformation and color, we like to refer to it as a "molecular chameleon". The term "catenane chameleons" has already been used: D. A. Leigh, K. Moody, J. P. Smart, K. J. Watson, A. M. Z. Slawin, Angew. Chem. 1996, 108, 326-331; Angew. Chem. Int. Ed. Engl. 1996, 35, 306-310.
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    • Leigh, D.A.1    Moody, K.2    Smart, J.P.3    Watson, K.J.4    Slawin, A.M.Z.5
  • 36
    • 33748216037 scopus 로고    scopus 로고
    • 4+ is a changeable entity, both in terms of its conformation and color, we like to refer to it as a "molecular chameleon". The term "catenane chameleons" has already been used: D. A. Leigh, K. Moody, J. P. Smart, K. J. Watson, A. M. Z. Slawin, Angew. Chem. 1996, 108, 326-331; Angew. Chem. Int. Ed. Engl. 1996, 35, 306-310.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 306-310
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    • note
    • -3. 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-100741. 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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    • note
    • [5a] are 5 and 22°, respectively.
  • 39
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    • note
    • 1H NMR: δ(α-bipyridinium-H) = 8.50, 8.63, 8.68, 8.76.8.77, 8.80, 9.14, 9.19; δ(β-bipyridinium-H) = 7.02, 7.06, 7.23, 7.27, 7.32, 7.34, 7.40, 7.48.
  • 41
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    • note
    • c. [20] The results of spectrophotometric titration were evaluated by a computer-assisted nonlinear least-square curve-fitting program (Ultrafit, Biosoft, Cambridge, 1992).
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    • a) For an excellent review on current developments in molecular switches, see M. D. Ward, Chem. Ind. 1997, 640-645.
    • (1997) Chem. Ind. , pp. 640-645
    • Ward, M.D.1
  • 45
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    • b) for our most recent publication on molecular switches, see M. Asakawa, P. R. Ashton, V. Balzani, A. Credi, C. Hamers, G. Mattersteig, M. Montalti, A. N. Shipway, N. Spencer, J. F. Stoddart, M. S. Tolley, M. Venturi, A. J. P. White, D. J. Williams, Angew. Chem. 1998, 110, 357-361; Angew. Chem. Int. Ed. 1998, 37, 333-337.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 333-337
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    • a) P. R. Ashton, A. Collins, M. C. T. Fyfe, P. T. Glink, S. Menzer, J. F. Stoddart, D. J. Williams, Angew. Chem. 1997, 109, 59-62; Angew. Chem. Int. Ed. Engl. 1997, 36, 59-62;
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    • Note added in proof (March 16, 1998): A self-complexing TTF macrocyle that can be switched has just appeared in the literature: see M. B. Nielsen, S. B. Nielsen, J. Becher, Chem. Commun. 1998, 475-476.
    • (1998) Chem. Commun. , pp. 475-476
    • Nielsen, M.B.1    Nielsen, S.B.2    Becher, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.