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1H NMR dilution experiment.
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40
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note
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A macrocyclic polyether of similar size to bis-p-phenylene-34-crown-10 but with no aromatic units, i.e. 36-crown-12, is unable to template the formation of a [2]catenane with cyclobis(paraquat-p-phenylene), as the other ring component, either at ambient or ultrahigh pressure.
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Bear, J.L.1
Ham, B.C.2
Kadish, K.M.3
Li, Y.L.4
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47
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2642693980
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note
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3CN solution at 303 K: it revealed that irradiation of a low intensity signal at δ 6.18 for the "alongside" hydroquinone ring protons leads to an enhancement of a signal at δ 3.75, for the "inside" hydroquinone ring protons.
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48
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2642599273
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note
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6 (25% at 12 kbar).
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49
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84986437005
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Macromodel V5.0
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Macromodel V5.0: Mohamadi, F.; Richards, N. G. J.; Guida, W. C.; Liskamp, R.; Lipton, M.; Caufield, C.; Chang, G.; Hendrickson, T.; Still, W. C. J. Comput. Chem. 1990, 11, 440-467.
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Mohamadi, F.1
Richards, N.G.J.2
Guida, W.C.3
Liskamp, R.4
Lipton, M.5
Caufield, C.6
Chang, G.7
Hendrickson, T.8
Still, W.C.9
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50
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0344778061
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Still, W. C.; Tempczyk, A.; Hawley, R. C.; Hendrickson, T. J. Am. Chem. Soc. 1990, 112, 6127-6129.
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Still, W.C.1
Tempczyk, A.2
Hawley, R.C.3
Hendrickson, T.4
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51
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0002624436
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Asakawa, M.; Ashton, P. R.; Boyd, S. E.; Brown, C. L.; Gillard, R. E.; Kocian, O.; Raymo, F. M.; Stoddart, J. F.; Tolley, M. S.; White, A. J. P.; Williams, D. J. J. Org. Chem. 1997, 62, 26-37.
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Asakawa, M.1
Ashton, P.R.2
Boyd, S.E.3
Brown, C.L.4
Gillard, R.E.5
Kocian, O.6
Raymo, F.M.7
Stoddart, J.F.8
Tolley, M.S.9
White, A.J.P.10
Williams, D.J.11
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52
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0000031451
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(a) Fletcher, D. A.; McMeeking, R. F.; Parkin, D. Chem. Inf. Comput. Sci. 1996, 36, 746-749.
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Fletcher, D.A.1
McMeeking, R.F.2
Parkin, D.3
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54
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2642653505
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4-). We feel that this nomenclature system facilitates the comparison of the UV-vis spectroscopic and electrochemical properties of the macrocyclic polyethers and catenanes with those of the reference compounds.
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55
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Spartan V4.1, Wavefunction Inc., 18401 Von Karman Ave., 370 Irvine CA 92715
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Spartan V4.1, Wavefunction Inc., 18401 Von Karman Ave., 370 Irvine CA 92715.
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