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PMI's and NDI's have been shown to be complementary to π-electron rich naphthalenes, and more recently in building "neutrally charged" catenanes. For recent work see: D. G. Hamilton, J. E. Davies, L. Prodi, and J. K. M. Sanders, Chem. Eur. J., 4, 608 (1998); D. G. Hamilton, N. Feeder, L. Prodi, S. J. Teat, W. Clegg, and J. K. M. Sanders, J. Am. Chem. Soc., 120, 1096 (1998).
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PMI's and NDI's have been shown to be complementary to π-electron rich naphthalenes, and more recently in building "neutrally charged" catenanes. For recent work see: D. G. Hamilton, J. E. Davies, L. Prodi, and J. K. M. Sanders, Chem. Eur. J., 4, 608 (1998); D. G. Hamilton, N. Feeder, L. Prodi, S. J. Teat, W. Clegg, and J. K. M. Sanders, J. Am. Chem. Soc., 120, 1096 (1998).
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19
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0007069485
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note
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a values, the predominance of a 1:1 complex is consistent with the low association constant and the results of the crystal structure data.
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20
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0007017922
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note
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2 = 0.057.
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21
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0032785675
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Martin, D.7
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