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For review articles, see a) D. Philp, J. F. Stoddart, Angew. Chem. 1996, 108, 1242-1286; Angew. Chem. Int. Ed. Engl. 1996, 55, 1154-1196;
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5
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For leading designs based on metal coordination, see: a) N. Takeda, K. Umemoto, K. Yamaguchi, M. Fujita, Nature 1999, 398, 794-796;
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b) B. C. Hamann, K. D. Shimizu, J. Rebek, Jr., Angew. Chem. 1996, 108, 1425-1427; Angew. Chem. Int. Ed. Engl. 1996, 35, 1326-1329;
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b) B. C. Hamann, K. D. Shimizu, J. Rebek, Jr., Angew. Chem. 1996, 108, 1425-1427; Angew. Chem. Int. Ed. Engl. 1996, 35, 1326-1329;
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10
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c) R. K. Castellano, D. M. Rudkevich, J. Rebek, Jr., J. Am. Chem. Soc. 1996, 118, 10002-10003;
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Castellano, R.K.1
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0002395534
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d) O. Mogck, V. Böhmer, W. Vogt, Tetrahedron 1996, 52, 8489-8496;
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1542502565
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e) O. Mogck, E. F. Paulus, V. Böhmer, I. Thondorf, W. Vogt, Chem. Commun. 1996, 2533-2534;
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f) O. Mogck, M. Pons, V. Böhmer, W. Vogt, J. Am. Chem. Soc. 1997, 119, 5706-5712;
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h) M. S. Brody, C. A. Schalley, D. M. Rudkevich, J. Rebek, Jr., Angew Chem. 1999, 111, 1738-1742; Angew. Chem. Int. Ed. 1999, 38, 1640-1644;
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h) M. S. Brody, C. A. Schalley, D. M. Rudkevich, J. Rebek, Jr., Angew Chem. 1999, 111, 1738-1742; Angew. Chem. Int. Ed. 1999, 38, 1640-1644;
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0033583713
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i) C. A. Schalley, R. K. Castellano, M. S. Brody, D. M. Rudkevich, G. Siuzdak, J. Rebek, Jr., J. Am. Chem. Soc. 1999, 121, 4568-4579.
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Schalley, C.A.1
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Siuzdak, G.5
Rebek J., Jr.6
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18
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0028126723
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For assemblies based on other H-bonded structural motifs, see a) K. Koh, K. Araki, S. Shinkai, Tetrahedron Lett. 1994, 35, 8255-8258;
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b) R. H. Vreekamp, W. Verboom, D. N. Reinhoudt, J. Org. Chem. 1996, 61, 4282-4288;
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Vreekamp, R.H.1
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0001282759
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c) A. Arduini, L. Domiano, L. Ogliosi, A. Pochini, A. Secchi, R. Ungaro, J. Org. Chem. 1997, 62, 7866-7868;
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d) J. J. González, P. Prados, J. de Mendoza, Angew. Chem. 1999, 111, 546-549; Angew. Chem. Int. Ed. 1999, 38, 525-528.
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d) J. J. González, P. Prados, J. de Mendoza, Angew. Chem. 1999, 111, 546-549; Angew. Chem. Int. Ed. 1999, 38, 525-528.
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23
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0032552135
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For a larger cavity based on resorcinarenes containing imido groups see: a) T. Heinz, D. M. Rudkevich, J. Rebek, Jr., Nature 1998, 394, 764-766;
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0000836244
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b) T. Heinz, D. M. Rudkevich, J. Rebek, Jr., Angew. Chem. 1999, 111, 1206-1209; Angew. Chem. Int. Ed. 1999, 38, 1136-1139;
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25
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0033583483
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b) T. Heinz, D. M. Rudkevich, J. Rebek, Jr., Angew. Chem. 1999, 111, 1206-1209; Angew. Chem. Int. Ed. 1999, 38, 1136-1139;
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26
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c) F. C. Tucci, D. M. Rudkevich, J. Rehek, Jr., J. Am. Chem. Soc. 1999, 121, 4928-4929.
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0004647517
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(Ed.: M. Pons), Kluwer, Dordrecht
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V. Böhmer, O. Mogck, M. Pops, E. F. Paulus, in NMR in Supramolecular Chemistry (Ed.: M. Pons), Kluwer, Dordrecht, 1999, pp. 45-60.
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J. P. M. van Duynhoven, R. G. Janssen, W. Verhoom, S. M. Franken, A. Casnati, A. Pochini, R. Ungaro, J. de Mendoza, P. M. Nieto, P. Prados, D. N. Reinhoudt, J. Am. Chem. Soc. 1994, 116, 5814-5822.
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29
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A. Casnati, L. Domianu, A. Pochini, R. Ungaro, M. Carramolino, J. O. Magrans, P. M. Nieto, J. López-Prados, P. Prados, J. de Mendoza, R. G. Janssen, W. Verboom, D. N. Reinhoudt, Tetrahedron 1995, 51, 12699-12720.
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De Mendoza, J.10
Janssen, R.G.11
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Reinhoudt, D.N.13
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30
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85080489328
-
-
note
-
3.
-
-
-
-
31
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0030481446
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The tailing of the peak is due to the slow dissociation of the dimer on the column. See: M. Mammen, E. E. Simanek, G. M. Whitesides, J. Am. Chem. Soc, 1996, 118, 12614-12623.
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J. Am. Chem. Soc
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Mammen, M.1
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Whitesides, G.M.3
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32
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0032572093
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The simultaneous observation of monomer and dimer has been reported previously in resorcinarene based capsules. See, for example: a) S. Ma, D. M. Rudkevich, J. Rebek, Jr., J. Am. Chem. Soc. 1998, 120, 4977-4981.
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Ma, S.1
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Rebek J., Jr.3
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34
-
-
85080505292
-
-
note
-
4]methanol at -50°C showed a mixture of dimer 1a-1a and monomer 1a; the monomer was the most abundant species.
-
-
-
-
35
-
-
85080612696
-
-
note
-
For the conformational control in a tetramethoxy calix[4]arene through self-assembly see ref. [3c].
-
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36
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33751498991
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C. Jaime, J. de Mendoza, P. Prados, P. M. Nieto, C. Sánchez, J. Org. Chem. 1991, 56, 3372-3376.
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Sánchez, C.5
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37
-
-
85080510048
-
-
note
-
This 2:1 stoicheometry was further assessed by examination of encapsulated benzene in a mixture of equimolar amounts of 1a-1a and 5,11,17,23 tetrakis-(N′-octylureyl)-25,26,27,28-tetrapropoxycalix[4]arene dimer (tetraureido calix[4]arene dimers encapsulate a single benzene molecule, see ref. [3b]). Identical integrals were observed for encapsulated benzene signals about δ=6.0 and 4.2.
-
-
-
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38
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85005576404
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A. Casnati, P. Minari, A. Pochini, R. Ungaro, W. F. Nijenhuis, F. de Jong, D. N. Reinhoudt, Isr. J. Chem. 1992, 32, 79-87.
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De Jong, F.6
Reinhoudt, D.N.7
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