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a) 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;
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Matthews, O.A.4
Raymo, F.M.5
Stoddart, J.F.6
Venturi, M.7
White, A.J.P.8
Williams, D.J.9
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0033893479
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c) C. L. Brown, U. Jonas, J. A. Preece, H. Ringsdorf, M. Seitz, J. F. Stoddart, Langmuir 2000, 16, 1924-1930;
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Brown, C.L.1
Jonas, U.2
Preece, J.A.3
Ringsdorf, H.4
Seitz, M.5
Stoddart, J.F.6
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0034245912
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d) M. Asakawa, M. Higuchi, G. Mattersteig, T. Nakamura, A. R. Pease, F. M. Raymo, T. Shimizu, J. F. Stoddart, Adv. Mater. 2000, 12, 1099-1102.
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Asakawa, M.1
Higuchi, M.2
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Nakamura, T.4
Pease, A.R.5
Raymo, F.M.6
Shimizu, T.7
Stoddart, J.F.8
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0344987778
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note
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Molecular modeling studies were performed using the MM2 force-field as implemented in Chem3D version 7.0. The molecule was "stretched" and then minimized to give the most linear conformation possible. The distance of 3.7 nm was measured from the center of the TTF unit to the center of the DNP ring system and can be compared to an overall length of approximately 9 nm for the rotaxane.
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75
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6844239208
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1H NMR spectrum and will not interfere with interpretation of the data, and 3) the solubilities of both the oxidant and its reduced form are good in the same solvents as the rotaxanes of interest. For details, see a) N. G. Connelly, W. E. Geiger, Chem. Rev. 1996, 96, 877-910; b) E. Steckhan, Top. Curr. Chem. 1987, 142, 1-69.
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, pp. 877-910
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Connelly, N.G.1
Geiger, W.E.2
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76
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6844239208
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1H NMR spectrum and will not interfere with interpretation of the data, and 3) the solubilities of both the oxidant and its reduced form are good in the same solvents as the rotaxanes of interest. For details, see a) N. G. Connelly, W. E. Geiger, Chem. Rev. 1996, 96, 877-910; b) E. Steckhan, Top. Curr. Chem. 1987, 142, 1-69.
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, vol.142
, pp. 1-69
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Steckhan, E.1
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77
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0345418971
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note
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1H DQF-COSY spectrum reproduced in Figure 4.
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78
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0033612015
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2+ has been reported previously, see P. R. Ashton, V. Balzani, J. Becher, A. Credi, M. C. T. Fyfe, G. Mattersteig, S. Menzer, M. B. Nielsen, F. M. Raymo, J. F. Stoddart, M. Venturi, D. J. Williams, J. Am. Chem. Soc. 1999, 121, 3951-3957.
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Ashton, P.R.1
Balzani, V.2
Becher, J.3
Credi, A.4
Fyfe, M.C.T.5
Mattersteig, G.6
Menzer, S.7
Nielsen, M.B.8
Raymo, F.M.9
Stoddart, J.F.10
Venturi, M.11
Williams, D.J.12
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79
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0344987777
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note
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1H DQF-COSY spectrum (Figure 4) for the oxidized [2]rotaxane. Additional evidence to support the assignments was obtained by peak integrations, as well as by monitoring the peaks during titration with the oxidant. Similar dramatic chemical shift changes have been observed in our laboratory for other TTF-containing compounds upon oxidation.
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80
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0001469161
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S. Chia, J. Cao, J. F. Stoddart, J. I. Zink, Angew. Chem. 2001, 113, 2513-2517; Angew. Chem. Int. Ed. 2001, 40, 2447-2451.
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Chia, S.1
Cao, J.2
Stoddart, J.F.3
Zink, J.I.4
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81
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0035796698
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S. Chia, J. Cao, J. F. Stoddart, J. I. Zink, Angew. Chem. 2001, 113, 2513-2517; Angew. Chem. Int. Ed. 2001, 40, 2447-2451.
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