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36
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0001513586
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For inorganic entities, see for instance: a) B. Hasenknopf, J.-M. Lehn, B. O. Kneisel, G. Baum, D. Fenske, Angew. Chem. 1996, 108, 1987;
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b) B. Hasenknopf, J.-M. Lehn, N. Boumediene, A. Dupont-Gervais, A. Van Dorsselaer, B. Kneisel, D. Fenske, J. Am. Chem. Soc. 1997, 119, 10 956;
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39
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c) J. S. Fleming, K. L. V. Mann, C.-A. Carraz, E. Psillakis, J. C. Jeffery, J. A. McCleverty, M. D. Ward, Angew. Chem. 1998, 110, 1315;
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d) I. Hue, M. J. Krische, D. P. Funeriu, J.-M. Lehn, Eur. J. Inorg. Chem. 1999, 1415;
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54
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0002824017
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(Eds.: R. Ungaro, E. Dalcanale), Kluwer, Dordrecht, (The Netherlands)
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b) J.-M. Lehn in Supramolecular Science: Where It Is and Where It Is Going (Eds.: R. Ungaro, E. Dalcanale), Kluwer, Dordrecht, (The Netherlands), 1999, p. 287.
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58
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24344500145
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b) J.-M. Lehn, Prog. Polym. Sci. 2005, 30, 814, and references therein.
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a) N. Giuseppone, J.-L. Schmitt, J.-M. Lehn, Angew. Chem. 2004, 116, 5010;
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Giuseppone, N.1
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63
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1542397425
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b) For an earlier example, concerning a constitutional reorganization of equilibrating coordination compounds driven by crystallization, see: P. N. W. Baxter, J.-M. Lehn, K. Rissanen, Chem. Commun. 1997, 1323;
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Baxter, P.N.W.1
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64
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0034680511
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or c) by solvent composition, see: P. N. W. Baxter, R. G. Khoury, J.-M. Lehn, G. Baum, D. Fenske, Chem. Eur. J. 2000, 6, 4140.
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65
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-
32944480399
-
-
note
-
The conversion corresponds to the ratio of the sum of imine-type products over the sum of imine-type products plus the sum of the remaining aldehydes (which is equal to the total aldehydes introduced): ∑(imines)/[∑(imines) + ∑(aldehydes)], as directly determined by integration of the corresponding proton NMR signals. The composition is defined as (imine)/∑(imines), and the expression is given by: (imine)/[∑(imines) + ∑(aldehydes)].
-
-
-
-
66
-
-
32944460325
-
-
note
-
-1 M, involved a sequence of four heating (358 K, 24 h)/cooling (298 K, 24 h) cycles and showed no changes in the distribution of products for the same temperature.
-
-
-
-
67
-
-
32944459468
-
-
note
-
The system was heated up to 428 K, but above 368 K, unassigned supplementary signals were observed, so that the study was limited to the 298-368 K range.
-
-
-
-
68
-
-
32944464854
-
-
note
-
[16b]
-
-
-
-
71
-
-
0003882087
-
-
(Ed.: S. Patai), Interscience, New York
-
Numerous detailed studies of imine formation have been performed in the literature; for general presentations, see for instance: a) The Chemistry of the Carbon-Nitrogen Double Bond (Ed.: S. Patai), Interscience, New York, 1970;
-
(1970)
The Chemistry of the Carbon-nitrogen Double Bond
-
-
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72
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-
0001311980
-
-
(Ed.: I. O. Sutherland), Pergamon, Oxford
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b) G. Tennant in Comprehensive Dynamic Chemistry Vol. 2 (Ed.: I. O. Sutherland), Pergamon, Oxford, 1979, p. 385;
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(1979)
Comprehensive Dynamic Chemistry
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, pp. 385
-
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Tennant, G.1
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76
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-
17644404350
-
-
and references therein
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N. Giuseppone, J.-L. Schmitt, E. Schwartz, J.-M. Lehn, J. Am. Chem. Soc. 2005, 127, 5528, and references therein.
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J. Am. Chem. Soc.
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-
Giuseppone, N.1
Schmitt, J.-L.2
Schwartz, E.3
Lehn, J.-M.4
-
77
-
-
32944474129
-
-
note
-
a) The present compounds display fluorescence that is affected markedly by the acidity and temperature; but the variations observed are very complex and have not been analyzed at this stage;
-
-
-
-
78
-
-
32944474355
-
-
following paper
-
b) polyimines containing fluorenyl groups present marked modification in spectral properties on reorganization: N. Giuseppone, G. Fuks, J.-M. Lehn, Chem. Eur. J. 2006, 12, 1723 (following paper);
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Giuseppone, N.1
Fuks, G.2
Lehn, J.-M.3
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79
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4444331253
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c) energy transfer between groups linked by an imine functional group has been described: W. G. Skene, S. Dufresne, Org. Lett. 2004, 6, 2949.
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Skene, W.G.1
Dufresne, S.2
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