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Volumn , Issue 12, 1998, Pages 2689-2702

The Modular Approach in Supramolecular Chemistry

Author keywords

Building blocks; Calix 4 arenes; Modular approach; Resorcin 4 arenes; Supramolecular chemistry

Indexed keywords


EID: 2742521374     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1099-0690(199812)1998:12<2689::aid-ejoc2689>3.0.co;2-9     Document Type: Article
Times cited : (74)

References (184)
  • 1
    • 21844512054 scopus 로고
    • 15,19]octacosa-1(25),3,5,7(28),9,11,13(27),15,17, 19(26),21,23-dodecacne. For simplicity reasons we have given each of the calix[4]arene aromatic rings a number (1-4); therefore, we call a 5,17-difunctionalized calix[4]arene a 1,3-difunctionalized calix[4]arene. [1a] T. Kappe, J. Incl. Phenom. Mol. Recogn. 1994, 19, 3-15. - [1b] V. Böhmer, Angew. Chem. Int. Ed. Engl 1995, 34, 713-745; Angew. Chem. 1995, 107, 785-818. [1c] C. D. Gutsche, Calixarenes, Monographs in Supramolecular Chemistry, vol. 1 (Ed.: J. F. Stoddart), The Royal Society of Chemistry, Cambridge, 1989. - [1d] J.-D. Van Loon, J. F. Heida, W. Verboom, D. N. Reinhoudt. Recl. Trav Chim. Pays-Bas 1992, 111, 353-359. - [1e] J.-D. Van Loon, W. Verboom, D. N. Reinhoudt, Org. Prep. Proced. Int. 1992, 24, 437-462. [1f] A. Ikeda, S. Shinkai, Chem. Rev. 1997, 97, 1713-1734. - [1g] V. Böhmer. Liebigs Ann./ Recl. 1997, 2019-2030.
    • (1994) J. Incl. Phenom. Mol. Recogn. , vol.19 , pp. 3-15
    • Kappe, T.1
  • 2
    • 33748539998 scopus 로고
    • 15,19]octacosa-1(25),3,5,7(28),9,11,13(27),15,17, 19(26),21,23-dodecacne. For simplicity reasons we have given each of the calix[4]arene aromatic rings a number (1-4); therefore, we call a 5,17-difunctionalized calix[4]arene a 1,3-difunctionalized calix[4]arene. [1a] T. Kappe, J. Incl. Phenom. Mol. Recogn. 1994, 19, 3-15. - [1b] V. Böhmer, Angew. Chem. Int. Ed. Engl 1995, 34, 713-745; Angew. Chem. 1995, 107, 785-818. [1c] C. D. Gutsche, Calixarenes, Monographs in Supramolecular Chemistry, vol. 1 (Ed.: J. F. Stoddart), The Royal Society of Chemistry, Cambridge, 1989. - [1d] J.-D. Van Loon, J. F. Heida, W. Verboom, D. N. Reinhoudt. Recl. Trav Chim. Pays-Bas 1992, 111, 353-359. - [1e] J.-D. Van Loon, W. Verboom, D. N. Reinhoudt, Org. Prep. Proced. Int. 1992, 24, 437-462. [1f] A. Ikeda, S. Shinkai, Chem. Rev. 1997, 97, 1713-1734. - [1g] V. Böhmer. Liebigs Ann./ Recl. 1997, 2019-2030.
    • (1995) Angew. Chem. Int. Ed. Engl , vol.34 , pp. 713-745
    • Böhmer, V.1
  • 3
    • 0000948055 scopus 로고
    • 15,19]octacosa-1(25),3,5,7(28),9,11,13(27),15,17, 19(26),21,23-dodecacne. For simplicity reasons we have given each of the calix[4]arene aromatic rings a number (1-4); therefore, we call a 5,17-difunctionalized calix[4]arene a 1,3-difunctionalized calix[4]arene. [1a] T. Kappe, J. Incl. Phenom. Mol. Recogn. 1994, 19, 3-15. - [1b] V. Böhmer, Angew. Chem. Int. Ed. Engl 1995, 34, 713-745; Angew. Chem. 1995, 107, 785-818. [1c] C. D. Gutsche, Calixarenes, Monographs in Supramolecular Chemistry, vol. 1 (Ed.: J. F. Stoddart), The Royal Society of Chemistry, Cambridge, 1989. - [1d] J.-D. Van Loon, J. F. Heida, W. Verboom, D. N. Reinhoudt. Recl. Trav Chim. Pays-Bas 1992, 111, 353-359. - [1e] J.-D. Van Loon, W. Verboom, D. N. Reinhoudt, Org. Prep. Proced. Int. 1992, 24, 437-462. [1f] A. Ikeda, S. Shinkai, Chem. Rev. 1997, 97, 1713-1734. - [1g] V. Böhmer. Liebigs Ann./ Recl. 1997, 2019-2030.
    • (1995) Angew. Chem. , vol.107 , pp. 785-818
  • 4
    • 0004146786 scopus 로고
    • Monographs in Supramolecular Chemistry, (Ed.: J. F. Stoddart), The Royal Society of Chemistry, Cambridge
    • 15,19]octacosa-1(25),3,5,7(28),9,11,13(27),15,17, 19(26),21,23-dodecacne. For simplicity reasons we have given each of the calix[4]arene aromatic rings a number (1-4); therefore, we call a 5,17-difunctionalized calix[4]arene a 1,3-difunctionalized calix[4]arene. [1a] T. Kappe, J. Incl. Phenom. Mol. Recogn. 1994, 19, 3-15. - [1b] V. Böhmer, Angew. Chem. Int. Ed. Engl 1995, 34, 713-745; Angew. Chem. 1995, 107, 785-818. [1c] C. D. Gutsche, Calixarenes, Monographs in Supramolecular Chemistry, vol. 1 (Ed.: J. F. Stoddart), The Royal Society of Chemistry, Cambridge, 1989. - [1d] J.-D. Van Loon, J. F. Heida, W. Verboom, D. N. Reinhoudt. Recl. Trav Chim. Pays-Bas 1992, 111, 353-359. - [1e] J.-D. Van Loon, W. Verboom, D. N. Reinhoudt, Org. Prep. Proced. Int. 1992, 24, 437-462. [1f] A. Ikeda, S. Shinkai, Chem. Rev. 1997, 97, 1713-1734. - [1g] V. Böhmer. Liebigs Ann./ Recl. 1997, 2019-2030.
    • (1989) Calixarenes , vol.1
    • Gutsche, C.D.1
  • 5
    • 30244527308 scopus 로고
    • 15,19]octacosa-1(25),3,5,7(28),9,11,13(27),15,17, 19(26),21,23-dodecacne. For simplicity reasons we have given each of the calix[4]arene aromatic rings a number (1-4); therefore, we call a 5,17-difunctionalized calix[4]arene a 1,3-difunctionalized calix[4]arene. [1a] T. Kappe, J. Incl. Phenom. Mol. Recogn. 1994, 19, 3-15. - [1b] V. Böhmer, Angew. Chem. Int. Ed. Engl 1995, 34, 713-745; Angew. Chem. 1995, 107, 785-818. [1c] C. D. Gutsche, Calixarenes, Monographs in Supramolecular Chemistry, vol. 1 (Ed.: J. F. Stoddart), The Royal Society of Chemistry, Cambridge, 1989. - [1d] J.-D. Van Loon, J. F. Heida, W. Verboom, D. N. Reinhoudt. Recl. Trav Chim. Pays-Bas 1992, 111, 353-359. - [1e] J.-D. Van Loon, W. Verboom, D. N. Reinhoudt, Org. Prep. Proced. Int. 1992, 24, 437-462. [1f] A. Ikeda, S. Shinkai, Chem. Rev. 1997, 97, 1713-1734. - [1g] V. Böhmer. Liebigs Ann./ Recl. 1997, 2019-2030.
    • (1992) Recl. Trav Chim. Pays-Bas , vol.111 , pp. 353-359
    • Van Loon, J.-D.1    Heida, J.F.2    Verboom, W.3    Reinhoudt, D.N.4
  • 6
    • 0000537860 scopus 로고
    • 15,19]octacosa-1(25),3,5,7(28),9,11,13(27),15,17, 19(26),21,23-dodecacne. For simplicity reasons we have given each of the calix[4]arene aromatic rings a number (1-4); therefore, we call a 5,17-difunctionalized calix[4]arene a 1,3-difunctionalized calix[4]arene. [1a] T. Kappe, J. Incl. Phenom. Mol. Recogn. 1994, 19, 3-15. - [1b] V. Böhmer, Angew. Chem. Int. Ed. Engl 1995, 34, 713-745; Angew. Chem. 1995, 107, 785-818. [1c] C. D. Gutsche, Calixarenes, Monographs in Supramolecular Chemistry, vol. 1 (Ed.: J. F. Stoddart), The Royal Society of Chemistry, Cambridge, 1989. - [1d] J.-D. Van Loon, J. F. Heida, W. Verboom, D. N. Reinhoudt. Recl. Trav Chim. Pays-Bas 1992, 111, 353-359. - [1e] J.-D. Van Loon, W. Verboom, D. N. Reinhoudt, Org. Prep. Proced. Int. 1992, 24, 437-462. [1f] A. Ikeda, S. Shinkai, Chem. Rev. 1997, 97, 1713-1734. - [1g] V. Böhmer. Liebigs Ann./ Recl. 1997, 2019-2030.
    • (1992) Org. Prep. Proced. Int. , vol.24 , pp. 437-462
    • Van Loon, J.-D.1    Verboom, W.2    Reinhoudt, D.N.3
  • 7
    • 0012694411 scopus 로고    scopus 로고
    • 15,19]octacosa-1(25),3,5,7(28),9,11,13(27),15,17, 19(26),21,23-dodecacne. For simplicity reasons we have given each of the calix[4]arene aromatic rings a number (1-4); therefore, we call a 5,17-difunctionalized calix[4]arene a 1,3-difunctionalized calix[4]arene. [1a] T. Kappe, J. Incl. Phenom. Mol. Recogn. 1994, 19, 3-15. - [1b] V. Böhmer, Angew. Chem. Int. Ed. Engl 1995, 34, 713-745; Angew. Chem. 1995, 107, 785-818. [1c] C. D. Gutsche, Calixarenes, Monographs in Supramolecular Chemistry, vol. 1 (Ed.: J. F. Stoddart), The Royal Society of Chemistry, Cambridge, 1989. - [1d] J.-D. Van Loon, J. F. Heida, W. Verboom, D. N. Reinhoudt. Recl. Trav Chim. Pays-Bas 1992, 111, 353-359. - [1e] J.-D. Van Loon, W. Verboom, D. N. Reinhoudt, Org. Prep. Proced. Int. 1992, 24, 437-462. [1f] A. Ikeda, S. Shinkai, Chem. Rev. 1997, 97, 1713-1734. - [1g] V. Böhmer. Liebigs Ann./ Recl. 1997, 2019-2030.
    • (1997) Chem. Rev. , vol.97 , pp. 1713-1734
    • Ikeda, A.1    Shinkai, S.2
  • 8
    • 33748822682 scopus 로고    scopus 로고
    • 15,19]octacosa-1(25),3,5,7(28),9,11,13(27),15,17, 19(26),21,23-dodecacne. For simplicity reasons we have given each of the calix[4]arene aromatic rings a number (1-4); therefore, we call a 5,17-difunctionalized calix[4]arene a 1,3-difunctionalized calix[4]arene. [1a] T. Kappe, J. Incl. Phenom. Mol. Recogn. 1994, 19, 3-15. - [1b] V. Böhmer, Angew. Chem. Int. Ed. Engl 1995, 34, 713-745; Angew. Chem. 1995, 107, 785-818. [1c] C. D. Gutsche, Calixarenes, Monographs in Supramolecular Chemistry, vol. 1 (Ed.: J. F. Stoddart), The Royal Society of Chemistry, Cambridge, 1989. - [1d] J.-D. Van Loon, J. F. Heida, W. Verboom, D. N. Reinhoudt. Recl. Trav Chim. Pays-Bas 1992, 111, 353-359. - [1e] J.-D. Van Loon, W. Verboom, D. N. Reinhoudt, Org. Prep. Proced. Int. 1992, 24, 437-462. [1f] A. Ikeda, S. Shinkai, Chem. Rev. 1997, 97, 1713-1734. - [1g] V. Böhmer. Liebigs Ann./ Recl. 1997, 2019-2030.
    • (1997) Liebigs Ann./ Recl. , pp. 2019-2030
    • Böhmer, V.1
  • 9
    • 0030021419 scopus 로고    scopus 로고
    • P. Timmerman, W. Verboom, D. N. Reinhoudt, Tetrahedron 1996, 52, 2663-2704. In the literature different names are given to resorcin[4]arenes. Because of the similarity with calix[4]arenes, names as "calix[4]resorcinarenes", "resorcinol-derived calix[4]arenes" or "resorcarenes" are used, however, names as Högberg compounds or octols are also used: see: [2a] A. G. S. Högberg, J. Am. Chem Soc. 1980, 102, 6046-6050. - [2b] A. G. S. Högberg, J. Org. Chem. 1980, 45, 4498-4500. In this review "resorcin[4]arene" will be used for the whole class of molecules, "octol" will be used for molecules with eight hydroxy groups (see formula 3), and "cavitand" will be used for the more rigid bridged compounds (see formula 4); see: [2c] D. J. Cram, J. M. Cram, Container Molecules and their Guests, Monographs in Supramolecular Chemistry, vol. 4 (Ed.: J. F. Stoddart), The Royal Society of Chemistry, Cambridge, 1994. Cram defines cavitands as synthetic "organic compounds with enforced cavities large enough to complex complementary organic compounds or ions"
    • (1996) Tetrahedron , vol.52 , pp. 2663-2704
    • Timmerman, P.1    Verboom, W.2    Reinhoudt, D.N.3
  • 10
    • 27544447505 scopus 로고
    • P. Timmerman, W. Verboom, D. N. Reinhoudt, Tetrahedron 1996, 52, 2663-2704. In the literature different names are given to resorcin[4]arenes. Because of the similarity with calix[4]arenes, names as "calix[4]resorcinarenes", "resorcinol-derived calix[4]arenes" or "resorcarenes" are used, however, names as Högberg compounds or octols are also used: see: [2a] A. G. S. Högberg, J. Am. Chem Soc. 1980, 102, 6046-6050. - [2b] A. G. S. Högberg, J. Org. Chem. 1980, 45, 4498-4500. In this review "resorcin[4]arene" will be used for the whole class of molecules, "octol" will be used for molecules with eight hydroxy groups (see formula 3), and "cavitand" will be used for the more rigid bridged compounds (see formula 4); see: [2c] D. J. Cram, J. M. Cram, Container Molecules and their Guests, Monographs in Supramolecular Chemistry, vol. 4 (Ed.: J. F. Stoddart), The Royal Society of Chemistry, Cambridge, 1994. Cram defines cavitands as synthetic "organic compounds with enforced cavities large enough to complex complementary organic compounds or ions"
    • (1980) J. Am. Chem Soc. , vol.102 , pp. 6046-6050
    • Högberg, A.G.S.1
  • 11
    • 27544475351 scopus 로고
    • P. Timmerman, W. Verboom, D. N. Reinhoudt, Tetrahedron 1996, 52, 2663-2704. In the literature different names are given to resorcin[4]arenes. Because of the similarity with calix[4]arenes, names as "calix[4]resorcinarenes", "resorcinol-derived calix[4]arenes" or "resorcarenes" are used, however, names as Högberg compounds or octols are also used: see: [2a] A. G. S. Högberg, J. Am. Chem Soc. 1980, 102, 6046-6050. - [2b] A. G. S. Högberg, J. Org. Chem. 1980, 45, 4498-4500. In this review "resorcin[4]arene" will be used for the whole class of molecules, "octol" will be used for molecules with eight hydroxy groups (see formula 3), and "cavitand" will be used for the more rigid bridged compounds (see formula 4); see: [2c] D. J. Cram, J. M. Cram, Container Molecules and their Guests, Monographs in Supramolecular Chemistry, vol. 4 (Ed.: J. F. Stoddart), The Royal Society of Chemistry, Cambridge, 1994. Cram defines cavitands as synthetic "organic compounds with enforced cavities large enough to complex complementary organic compounds or ions"
    • (1980) J. Org. Chem. , vol.45 , pp. 4498-4500
    • Högberg, A.G.S.1
  • 12
    • 0003932069 scopus 로고
    • Monographs in Supramolecular Chemistry, (Ed.: J. F. Stoddart), The Royal Society of Chemistry, Cambridge
    • P. Timmerman, W. Verboom, D. N. Reinhoudt, Tetrahedron 1996, 52, 2663-2704. In the literature different names are given to resorcin[4]arenes. Because of the similarity with calix[4]arenes, names as "calix[4]resorcinarenes", "resorcinol-derived calix[4]arenes" or "resorcarenes" are used, however, names as Högberg compounds or octols are also used: see: [2a] A. G. S. Högberg, J. Am. Chem Soc. 1980, 102, 6046-6050. - [2b] A. G. S. Högberg, J. Org. Chem. 1980, 45, 4498-4500. In this review "resorcin[4]arene" will be used for the whole class of molecules, "octol" will be used for molecules with eight hydroxy groups (see formula 3), and "cavitand" will be used for the more rigid bridged compounds (see formula 4); see: [2c] D. J. Cram, J. M. Cram, Container Molecules and their Guests, Monographs in Supramolecular Chemistry, vol. 4 (Ed.: J. F. Stoddart), The Royal Society of Chemistry, Cambridge, 1994. Cram defines cavitands as synthetic "organic compounds with enforced cavities large enough to complex complementary organic compounds or ions"
    • (1994) Container Molecules and Their Guests , vol.4
    • Cram, D.J.1    Cram, J.M.2
  • 13
    • 0004063197 scopus 로고
    • Topics in Inclusion Science, Kiuwer Academic Publishers, Dordrecht
    • J. Szejtli, Cyclodextrin Technology, Topics in Inclusion Science, Kiuwer Academic Publishers, Dordrecht, 1988.
    • (1988) Cyclodextrin Technology
    • Szejtli, J.1
  • 14
    • 0000577119 scopus 로고    scopus 로고
    • Cryptophanes
    • (Ed.: F. Vögtle), Pergamon, Oxford, chapter 11
    • A. Collet, "Cryptophanes", in Comprehensive Supramolecular Chemistry, vol. 2 (Ed.: F. Vögtle), Pergamon, Oxford, 1996, chapter 11.
    • (1996) Comprehensive Supramolecular Chemistry , vol.2
    • Collet, A.1
  • 21
    • 0006787012 scopus 로고    scopus 로고
    • Synthetic Receptors: A Modular Approach to Large Structures
    • (Eds., G. Tsoucaris, J. L. Atwood, J. Lipkowski), Kiuwer Academic Publishers, Dordrecht, and references cited therein
    • I. Higler, W. Verboom, D. N. Reinhoudt, "Synthetic Receptors: a Modular Approach to Large Structures", in Crystallography of Supramolecular Compounds (Eds., G. Tsoucaris, J. L. Atwood, J. Lipkowski), Kiuwer Academic Publishers, Dordrecht, 1996, pp 347-368, and references cited therein.
    • (1996) Crystallography of Supramolecular Compounds , pp. 347-368
    • Higler, I.1    Verboom, W.2    Reinhoudt, D.N.3
  • 24
    • 4243092100 scopus 로고    scopus 로고
    • For a review on the formation of artificial receptors by metaltemplated self-assembly see: B. Linton, A. Hamilton, Chem. Rev 1997, 97, 1669-1680. For some examples of metal-coordinated catenaries, see: [10a] D. J. Cárdenas, P. Gaviña, J.-P. Sauvage, J Am. Chem. Soc. 1997, 119, 2656-2664. - [10b] B. Mohr, M. Weck, J.-P. Sauvage, R. H. Grubbs, Angew. Chem. Int. Ed. Engl. 1997, 36, 1308-1310; Angew. Chem. 1997, 109, 1365-1367. - [10c] N. Solladié, J.-C. Chambron, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. Int. Ed. Engl. 1996, 35, 906-909; Angew. Chem. 1996, 108, 957-960. For some examples of metal-coordinated helicates, grid structures, and a metallic rotaxane see: - [10d] B. Hasenknopf, J.-M. Lehn, B. O. Kneisel, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1996, 35, 1838-1840; Angew. Chem. 1996, 108, 1987-1990. - [10e] D. M. Bassani, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem Int. Ed. Engl. 1997, 36, 1845-1847; Angew. Chem. 1997, 109, 1931-1933. - [10f] G. S. Hanan, D. Volkmer, U. S. Schubert, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1997, 36, 1842-1844; Angew. Chem. 1997, 109, 1929-1931. - [10g] P. N. W. Baxter, H. Sleiman, J.-M. Lehn, K. Rissanen, Angew. Chem. Int. Ed. Engl. 1997, 36, 1294-1296; Angew. Chem. 1997, 109, 1350-1352.
    • (1997) Chem. Rev , vol.97 , pp. 1669-1680
    • Linton, B.1    Hamilton, A.2
  • 25
    • 0040502092 scopus 로고    scopus 로고
    • For a review on the formation of artificial receptors by metaltemplated self-assembly see: B. Linton, A. Hamilton, Chem. Rev 1997, 97, 1669-1680. For some examples of metal-coordinated catenaries, see: [10a] D. J. Cárdenas, P. Gaviña, J.-P. Sauvage, J Am. Chem. Soc. 1997, 119, 2656-2664. - [10b] B. Mohr, M. Weck, J.-P. Sauvage, R. H. Grubbs, Angew. Chem. Int. Ed. Engl. 1997, 36, 1308-1310; Angew. Chem. 1997, 109, 1365-1367. - [10c] N. Solladié, J.-C. Chambron, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. Int. Ed. Engl. 1996, 35, 906-909; Angew. Chem. 1996, 108, 957-960. For some examples of metal-coordinated helicates, grid structures, and a metallic rotaxane see: - [10d] B. Hasenknopf, J.-M. Lehn, B. O. Kneisel, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1996, 35, 1838-1840; Angew. Chem. 1996, 108, 1987-1990. - [10e] D. M. Bassani, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem Int. Ed. Engl. 1997, 36, 1845-1847; Angew. Chem. 1997, 109, 1931-1933. - [10f] G. S. Hanan, D. Volkmer, U. S. Schubert, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1997, 36, 1842-1844; Angew. Chem. 1997, 109, 1929-1931. - [10g] P. N. W. Baxter, H. Sleiman, J.-M. Lehn, K. Rissanen, Angew. Chem. Int. Ed. Engl. 1997, 36, 1294-1296; Angew. Chem. 1997, 109, 1350-1352.
    • (1997) J Am. Chem. Soc. , vol.119 , pp. 2656-2664
    • Cárdenas, D.J.1    Gaviña, P.2    Sauvage, J.-P.3
  • 26
    • 0030738752 scopus 로고    scopus 로고
    • For a review on the formation of artificial receptors by metaltemplated self-assembly see: B. Linton, A. Hamilton, Chem. Rev 1997, 97, 1669-1680. For some examples of metal-coordinated catenaries, see: [10a] D. J. Cárdenas, P. Gaviña, J.-P. Sauvage, J Am. Chem. Soc. 1997, 119, 2656-2664. - [10b] B. Mohr, M. Weck, J.-P. Sauvage, R. H. Grubbs, Angew. Chem. Int. Ed. Engl. 1997, 36, 1308-1310; Angew. Chem. 1997, 109, 1365-1367. - [10c] N. Solladié, J.-C. Chambron, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. Int. Ed. Engl. 1996, 35, 906-909; Angew. Chem. 1996, 108, 957-960. For some examples of metal-coordinated helicates, grid structures, and a metallic rotaxane see: - [10d] B. Hasenknopf, J.-M. Lehn, B. O. Kneisel, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1996, 35, 1838-1840; Angew. Chem. 1996, 108, 1987-1990. - [10e] D. M. Bassani, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem Int. Ed. Engl. 1997, 36, 1845-1847; Angew. Chem. 1997, 109, 1931-1933. - [10f] G. S. Hanan, D. Volkmer, U. S. Schubert, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1997, 36, 1842-1844; Angew. Chem. 1997, 109, 1929-1931. - [10g] P. N. W. Baxter, H. Sleiman, J.-M. Lehn, K. Rissanen, Angew. Chem. Int. Ed. Engl. 1997, 36, 1294-1296; Angew. Chem. 1997, 109, 1350-1352.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 1308-1310
    • Mohr, B.1    Weck, M.2    Sauvage, J.-P.3    Grubbs, R.H.4
  • 27
    • 0000118115 scopus 로고    scopus 로고
    • For a review on the formation of artificial receptors by metaltemplated self-assembly see: B. Linton, A. Hamilton, Chem. Rev 1997, 97, 1669-1680. For some examples of metal-coordinated catenaries, see: [10a] D. J. Cárdenas, P. Gaviña, J.-P. Sauvage, J Am. Chem. Soc. 1997, 119, 2656-2664. - [10b] B. Mohr, M. Weck, J.-P. Sauvage, R. H. Grubbs, Angew. Chem. Int. Ed. Engl. 1997, 36, 1308-1310; Angew. Chem. 1997, 109, 1365-1367. - [10c] N. Solladié, J.-C. Chambron, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. Int. Ed. Engl. 1996, 35, 906-909; Angew. Chem. 1996, 108, 957-960. For some examples of metal-coordinated helicates, grid structures, and a metallic rotaxane see: - [10d] B. Hasenknopf, J.-M. Lehn, B. O. Kneisel, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1996, 35, 1838-1840; Angew. Chem. 1996, 108, 1987-1990. - [10e] D. M. Bassani, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem Int. Ed. Engl. 1997, 36, 1845-1847; Angew. Chem. 1997, 109, 1931-1933. - [10f] G. S. Hanan, D. Volkmer, U. S. Schubert, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1997, 36, 1842-1844; Angew. Chem. 1997, 109, 1929-1931. - [10g] P. N. W. Baxter, H. Sleiman, J.-M. Lehn, K. Rissanen, Angew. Chem. Int. Ed. Engl. 1997, 36, 1294-1296; Angew. Chem. 1997, 109, 1350-1352.
    • (1997) Angew. Chem. , vol.109 , pp. 1365-1367
  • 28
    • 33748725372 scopus 로고    scopus 로고
    • For a review on the formation of artificial receptors by metaltemplated self-assembly see: B. Linton, A. Hamilton, Chem. Rev 1997, 97, 1669-1680. For some examples of metal-coordinated catenaries, see: [10a] D. J. Cárdenas, P. Gaviña, J.-P. Sauvage, J Am. Chem. Soc. 1997, 119, 2656-2664. - [10b] B. Mohr, M. Weck, J.-P. Sauvage, R. H. Grubbs, Angew. Chem. Int. Ed. Engl. 1997, 36, 1308-1310; Angew. Chem. 1997, 109, 1365-1367. - [10c] N. Solladié, J.-C. Chambron, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. Int. Ed. Engl. 1996, 35, 906-909; Angew. Chem. 1996, 108, 957-960. For some examples of metal-coordinated helicates, grid structures, and a metallic rotaxane see: - [10d] B. Hasenknopf, J.-M. Lehn, B. O. Kneisel, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1996, 35, 1838-1840; Angew. Chem. 1996, 108, 1987-1990. - [10e] D. M. Bassani, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem Int. Ed. Engl. 1997, 36, 1845-1847; Angew. Chem. 1997, 109, 1931-1933. - [10f] G. S. Hanan, D. Volkmer, U. S. Schubert, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1997, 36, 1842-1844; Angew. Chem. 1997, 109, 1929-1931. - [10g] P. N. W. Baxter, H. Sleiman, J.-M. Lehn, K. Rissanen, Angew. Chem. Int. Ed. Engl. 1997, 36, 1294-1296; Angew. Chem. 1997, 109, 1350-1352.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 906-909
    • Solladié, N.1    Chambron, J.-C.2    Dietrich-Buchecker, C.O.3    Sauvage, J.-P.4
  • 29
    • 0005498238 scopus 로고    scopus 로고
    • For a review on the formation of artificial receptors by metaltemplated self-assembly see: B. Linton, A. Hamilton, Chem. Rev 1997, 97, 1669-1680. For some examples of metal-coordinated catenaries, see: [10a] D. J. Cárdenas, P. Gaviña, J.-P. Sauvage, J Am. Chem. Soc. 1997, 119, 2656-2664. - [10b] B. Mohr, M. Weck, J.-P. Sauvage, R. H. Grubbs, Angew. Chem. Int. Ed. Engl. 1997, 36, 1308-1310; Angew. Chem. 1997, 109, 1365-1367. - [10c] N. Solladié, J.-C. Chambron, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. Int. Ed. Engl. 1996, 35, 906-909; Angew. Chem. 1996, 108, 957-960. For some examples of metal-coordinated helicates, grid structures, and a metallic rotaxane see: - [10d] B. Hasenknopf, J.-M. Lehn, B. O. Kneisel, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1996, 35, 1838-1840; Angew. Chem. 1996, 108, 1987-1990. - [10e] D. M. Bassani, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem Int. Ed. Engl. 1997, 36, 1845-1847; Angew. Chem. 1997, 109, 1931-1933. - [10f] G. S. Hanan, D. Volkmer, U. S. Schubert, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1997, 36, 1842-1844; Angew. Chem. 1997, 109, 1929-1931. - [10g] P. N. W. Baxter, H. Sleiman, J.-M. Lehn, K. Rissanen, Angew. Chem. Int. Ed. Engl. 1997, 36, 1294-1296; Angew. Chem. 1997, 109, 1350-1352.
    • (1996) Angew. Chem. , vol.108 , pp. 957-960
  • 30
    • 0030498846 scopus 로고    scopus 로고
    • For a review on the formation of artificial receptors by metaltemplated self-assembly see: B. Linton, A. Hamilton, Chem. Rev 1997, 97, 1669-1680. For some examples of metal-coordinated catenaries, see: [10a] D. J. Cárdenas, P. Gaviña, J.-P. Sauvage, J Am. Chem. Soc. 1997, 119, 2656-2664. - [10b] B. Mohr, M. Weck, J.-P. Sauvage, R. H. Grubbs, Angew. Chem. Int. Ed. Engl. 1997, 36, 1308-1310; Angew. Chem. 1997, 109, 1365-1367. - [10c] N. Solladié, J.-C. Chambron, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. Int. Ed. Engl. 1996, 35, 906-909; Angew. Chem. 1996, 108, 957-960. For some examples of metal-coordinated helicates, grid structures, and a metallic rotaxane see: - [10d] B. Hasenknopf, J.-M. Lehn, B. O. Kneisel, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1996, 35, 1838-1840; Angew. Chem. 1996, 108, 1987-1990. - [10e] D. M. Bassani, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem Int. Ed. Engl. 1997, 36, 1845-1847; Angew. Chem. 1997, 109, 1931-1933. - [10f] G. S. Hanan, D. Volkmer, U. S. Schubert, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1997, 36, 1842-1844; Angew. Chem. 1997, 109, 1929-1931. - [10g] P. N. W. Baxter, H. Sleiman, J.-M. Lehn, K. Rissanen, Angew. Chem. Int. Ed. Engl. 1997, 36, 1294-1296; Angew. Chem. 1997, 109, 1350-1352.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 1838-1840
    • Hasenknopf, B.1    Lehn, J.-M.2    Kneisel, B.O.3    Baum, G.4    Fenske, D.5
  • 31
    • 0001513586 scopus 로고    scopus 로고
    • For a review on the formation of artificial receptors by metaltemplated self-assembly see: B. Linton, A. Hamilton, Chem. Rev 1997, 97, 1669-1680. For some examples of metal-coordinated catenaries, see: [10a] D. J. Cárdenas, P. Gaviña, J.-P. Sauvage, J Am. Chem. Soc. 1997, 119, 2656-2664. - [10b] B. Mohr, M. Weck, J.-P. Sauvage, R. H. Grubbs, Angew. Chem. Int. Ed. Engl. 1997, 36, 1308-1310; Angew. Chem. 1997, 109, 1365-1367. - [10c] N. Solladié, J.-C. Chambron, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. Int. Ed. Engl. 1996, 35, 906-909; Angew. Chem. 1996, 108, 957-960. For some examples of metal-coordinated helicates, grid structures, and a metallic rotaxane see: - [10d] B. Hasenknopf, J.-M. Lehn, B. O. Kneisel, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1996, 35, 1838-1840; Angew. Chem. 1996, 108, 1987-1990. - [10e] D. M. Bassani, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem Int. Ed. Engl. 1997, 36, 1845-1847; Angew. Chem. 1997, 109, 1931-1933. - [10f] G. S. Hanan, D. Volkmer, U. S. Schubert, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1997, 36, 1842-1844; Angew. Chem. 1997, 109, 1929-1931. - [10g] P. N. W. Baxter, H. Sleiman, J.-M. Lehn, K. Rissanen, Angew. Chem. Int. Ed. Engl. 1997, 36, 1294-1296; Angew. Chem. 1997, 109, 1350-1352.
    • (1996) Angew. Chem. , vol.108 , pp. 1987-1990
  • 32
    • 0030766784 scopus 로고    scopus 로고
    • For a review on the formation of artificial receptors by metaltemplated self-assembly see: B. Linton, A. Hamilton, Chem. Rev 1997, 97, 1669-1680. For some examples of metal-coordinated catenaries, see: [10a] D. J. Cárdenas, P. Gaviña, J.-P. Sauvage, J Am. Chem. Soc. 1997, 119, 2656-2664. - [10b] B. Mohr, M. Weck, J.-P. Sauvage, R. H. Grubbs, Angew. Chem. Int. Ed. Engl. 1997, 36, 1308-1310; Angew. Chem. 1997, 109, 1365-1367. - [10c] N. Solladié, J.-C. Chambron, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. Int. Ed. Engl. 1996, 35, 906-909; Angew. Chem. 1996, 108, 957-960. For some examples of metal-coordinated helicates, grid structures, and a metallic rotaxane see: - [10d] B. Hasenknopf, J.-M. Lehn, B. O. Kneisel, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1996, 35, 1838-1840; Angew. Chem. 1996, 108, 1987-1990. - [10e] D. M. Bassani, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem Int. Ed. Engl. 1997, 36, 1845-1847; Angew. Chem. 1997, 109, 1931-1933. - [10f] G. S. Hanan, D. Volkmer, U. S. Schubert, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1997, 36, 1842-1844; Angew. Chem. 1997, 109, 1929-1931. - [10g] P. N. W. Baxter, H. Sleiman, J.-M. Lehn, K. Rissanen, Angew. Chem. Int. Ed. Engl. 1997, 36, 1294-1296; Angew. Chem. 1997, 109, 1350-1352.
    • (1997) Angew. Chem Int. Ed. Engl. , vol.36 , pp. 1845-1847
    • Bassani, D.M.1    Lehn, J.-M.2    Baum, G.3    Fenske, D.4
  • 33
    • 0001555353 scopus 로고    scopus 로고
    • For a review on the formation of artificial receptors by metaltemplated self-assembly see: B. Linton, A. Hamilton, Chem. Rev 1997, 97, 1669-1680. For some examples of metal-coordinated catenaries, see: [10a] D. J. Cárdenas, P. Gaviña, J.-P. Sauvage, J Am. Chem. Soc. 1997, 119, 2656-2664. - [10b] B. Mohr, M. Weck, J.-P. Sauvage, R. H. Grubbs, Angew. Chem. Int. Ed. Engl. 1997, 36, 1308-1310; Angew. Chem. 1997, 109, 1365-1367. - [10c] N. Solladié, J.-C. Chambron, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. Int. Ed. Engl. 1996, 35, 906-909; Angew. Chem. 1996, 108, 957-960. For some examples of metal-coordinated helicates, grid structures, and a metallic rotaxane see: - [10d] B. Hasenknopf, J.-M. Lehn, B. O. Kneisel, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1996, 35, 1838-1840; Angew. Chem. 1996, 108, 1987-1990. - [10e] D. M. Bassani, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem Int. Ed. Engl. 1997, 36, 1845-1847; Angew. Chem. 1997, 109, 1931-1933. - [10f] G. S. Hanan, D. Volkmer, U. S. Schubert, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1997, 36, 1842-1844; Angew. Chem. 1997, 109, 1929-1931. - [10g] P. N. W. Baxter, H. Sleiman, J.-M. Lehn, K. Rissanen, Angew. Chem. Int. Ed. Engl. 1997, 36, 1294-1296; Angew. Chem. 1997, 109, 1350-1352.
    • (1997) Angew. Chem. , vol.109 , pp. 1931-1933
  • 34
    • 0030864943 scopus 로고    scopus 로고
    • For a review on the formation of artificial receptors by metaltemplated self-assembly see: B. Linton, A. Hamilton, Chem. Rev 1997, 97, 1669-1680. For some examples of metal-coordinated catenaries, see: [10a] D. J. Cárdenas, P. Gaviña, J.-P. Sauvage, J Am. Chem. Soc. 1997, 119, 2656-2664. - [10b] B. Mohr, M. Weck, J.-P. Sauvage, R. H. Grubbs, Angew. Chem. Int. Ed. Engl. 1997, 36, 1308-1310; Angew. Chem. 1997, 109, 1365-1367. - [10c] N. Solladié, J.-C. Chambron, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. Int. Ed. Engl. 1996, 35, 906-909; Angew. Chem. 1996, 108, 957-960. For some examples of metal-coordinated helicates, grid structures, and a metallic rotaxane see: - [10d] B. Hasenknopf, J.-M. Lehn, B. O. Kneisel, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1996, 35, 1838-1840; Angew. Chem. 1996, 108, 1987-1990. - [10e] D. M. Bassani, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem Int. Ed. Engl. 1997, 36, 1845-1847; Angew. Chem. 1997, 109, 1931-1933. - [10f] G. S. Hanan, D. Volkmer, U. S. Schubert, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1997, 36, 1842-1844; Angew. Chem. 1997, 109, 1929-1931. - [10g] P. N. W. Baxter, H. Sleiman, J.-M. Lehn, K. Rissanen, Angew. Chem. Int. Ed. Engl. 1997, 36, 1294-1296; Angew. Chem. 1997, 109, 1350-1352.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 1842-1844
    • Hanan, G.S.1    Volkmer, D.2    Schubert, U.S.3    Lehn, J.-M.4    Baum, G.5    Fenske, D.6
  • 35
    • 0000614447 scopus 로고    scopus 로고
    • For a review on the formation of artificial receptors by metaltemplated self-assembly see: B. Linton, A. Hamilton, Chem. Rev 1997, 97, 1669-1680. For some examples of metal-coordinated catenaries, see: [10a] D. J. Cárdenas, P. Gaviña, J.-P. Sauvage, J Am. Chem. Soc. 1997, 119, 2656-2664. - [10b] B. Mohr, M. Weck, J.-P. Sauvage, R. H. Grubbs, Angew. Chem. Int. Ed. Engl. 1997, 36, 1308-1310; Angew. Chem. 1997, 109, 1365-1367. - [10c] N. Solladié, J.-C. Chambron, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. Int. Ed. Engl. 1996, 35, 906-909; Angew. Chem. 1996, 108, 957-960. For some examples of metal-coordinated helicates, grid structures, and a metallic rotaxane see: - [10d] B. Hasenknopf, J.-M. Lehn, B. O. Kneisel, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1996, 35, 1838-1840; Angew. Chem. 1996, 108, 1987-1990. - [10e] D. M. Bassani, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem Int. Ed. Engl. 1997, 36, 1845-1847; Angew. Chem. 1997, 109, 1931-1933. - [10f] G. S. Hanan, D. Volkmer, U. S. Schubert, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1997, 36, 1842-1844; Angew. Chem. 1997, 109, 1929-1931. - [10g] P. N. W. Baxter, H. Sleiman, J.-M. Lehn, K. Rissanen, Angew. Chem. Int. Ed. Engl. 1997, 36, 1294-1296; Angew. Chem. 1997, 109, 1350-1352.
    • (1997) Angew. Chem. , vol.109 , pp. 1929-1931
  • 36
    • 0030874426 scopus 로고    scopus 로고
    • For a review on the formation of artificial receptors by metaltemplated self-assembly see: B. Linton, A. Hamilton, Chem. Rev 1997, 97, 1669-1680. For some examples of metal-coordinated catenaries, see: [10a] D. J. Cárdenas, P. Gaviña, J.-P. Sauvage, J Am. Chem. Soc. 1997, 119, 2656-2664. - [10b] B. Mohr, M. Weck, J.-P. Sauvage, R. H. Grubbs, Angew. Chem. Int. Ed. Engl. 1997, 36, 1308-1310; Angew. Chem. 1997, 109, 1365-1367. - [10c] N. Solladié, J.-C. Chambron, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. Int. Ed. Engl. 1996, 35, 906-909; Angew. Chem. 1996, 108, 957-960. For some examples of metal-coordinated helicates, grid structures, and a metallic rotaxane see: - [10d] B. Hasenknopf, J.-M. Lehn, B. O. Kneisel, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1996, 35, 1838-1840; Angew. Chem. 1996, 108, 1987-1990. - [10e] D. M. Bassani, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem Int. Ed. Engl. 1997, 36, 1845-1847; Angew. Chem. 1997, 109, 1931-1933. - [10f] G. S. Hanan, D. Volkmer, U. S. Schubert, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1997, 36, 1842-1844; Angew. Chem. 1997, 109, 1929-1931. - [10g] P. N. W. Baxter, H. Sleiman, J.-M. Lehn, K. Rissanen, Angew. Chem. Int. Ed. Engl. 1997, 36, 1294-1296; Angew. Chem. 1997, 109, 1350-1352.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 1294-1296
    • Baxter, P.N.W.1    Sleiman, H.2    Lehn, J.-M.3    Rissanen, K.4
  • 37
    • 0001012204 scopus 로고    scopus 로고
    • For a review on the formation of artificial receptors by metaltemplated self-assembly see: B. Linton, A. Hamilton, Chem. Rev 1997, 97, 1669-1680. For some examples of metal-coordinated catenaries, see: [10a] D. J. Cárdenas, P. Gaviña, J.-P. Sauvage, J Am. Chem. Soc. 1997, 119, 2656-2664. - [10b] B. Mohr, M. Weck, J.-P. Sauvage, R. H. Grubbs, Angew. Chem. Int. Ed. Engl. 1997, 36, 1308-1310; Angew. Chem. 1997, 109, 1365-1367. - [10c] N. Solladié, J.-C. Chambron, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. Int. Ed. Engl. 1996, 35, 906-909; Angew. Chem. 1996, 108, 957-960. For some examples of metal-coordinated helicates, grid structures, and a metallic rotaxane see: - [10d] B. Hasenknopf, J.-M. Lehn, B. O. Kneisel, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1996, 35, 1838-1840; Angew. Chem. 1996, 108, 1987-1990. - [10e] D. M. Bassani, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem Int. Ed. Engl. 1997, 36, 1845-1847; Angew. Chem. 1997, 109, 1931-1933. - [10f] G. S. Hanan, D. Volkmer, U. S. Schubert, J.-M. Lehn, G. Baum, D. Fenske, Angew. Chem. Int. Ed. Engl. 1997, 36, 1842-1844; Angew. Chem. 1997, 109, 1929-1931. - [10g] P. N. W. Baxter, H. Sleiman, J.-M. Lehn, K. Rissanen, Angew. Chem. Int. Ed. Engl. 1997, 36, 1294-1296; Angew. Chem. 1997, 109, 1350-1352.
    • (1997) Angew. Chem. , vol.109 , pp. 1350-1352
  • 38
    • 0000329916 scopus 로고    scopus 로고
    • For reviews see: [11a] D. Philp, J. F. Stoddart, Angew. Chem. Int. Ed. Engl 1996, 35, 1155-1196; Angew. Chem. 1996, 108, 1242-1286. [11b] D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2828, and references cited therein. For some examples of cyclodextrin-based rotaxanes see: [11c] S. Anderson, T. D. W. Claridge, H. L. Anderson, Angew. Chem. Int. Ed. Engl. 1997, 36, 1310-1313; Angew. Chem 1997, 109, 1367-1370. - [11d] M. Born, H. Ritter, Angew. Chem. Int. Ed. Engl 1995, 34, 309-311; Angew. Chem. 1995, 107, 342-344.
    • (1996) Angew. Chem. Int. Ed. Engl , vol.35 , pp. 1155-1196
    • Philp, D.1    Stoddart, J.F.2
  • 39
    • 0000633029 scopus 로고    scopus 로고
    • For reviews see: [11a] D. Philp, J. F. Stoddart, Angew. Chem. Int. Ed. Engl 1996, 35, 1155-1196; Angew. Chem. 1996, 108, 1242-1286. [11b] D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2828, and references cited therein. For some examples of cyclodextrin-based rotaxanes see: [11c] S. Anderson, T. D. W. Claridge, H. L. Anderson, Angew. Chem. Int. Ed. Engl. 1997, 36, 1310-1313; Angew. Chem 1997, 109, 1367-1370. - [11d] M. Born, H. Ritter, Angew. Chem. Int. Ed. Engl 1995, 34, 309-311; Angew. Chem. 1995, 107, 342-344.
    • (1996) Angew. Chem. , vol.108 , pp. 1242-1286
  • 40
    • 2842587248 scopus 로고
    • and references cited therein.
    • For reviews see: [11a] D. Philp, J. F. Stoddart, Angew. Chem. Int. Ed. Engl 1996, 35, 1155-1196; Angew. Chem. 1996, 108, 1242-1286. [11b] D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2828, and references cited therein. For some examples of cyclodextrin-based rotaxanes see: [11c] S. Anderson, T. D. W. Claridge, H. L. Anderson, Angew. Chem. Int. Ed. Engl. 1997, 36, 1310-1313; Angew. Chem 1997, 109, 1367-1370. - [11d] M. Born, H. Ritter, Angew. Chem. Int. Ed. Engl 1995, 34, 309-311; Angew. Chem. 1995, 107, 342-344.
    • (1995) Chem. Rev. , vol.95 , pp. 2725-2828
    • Amabilino, D.B.1    Stoddart, J.F.2
  • 41
    • 0030793332 scopus 로고    scopus 로고
    • For reviews see: [11a] D. Philp, J. F. Stoddart, Angew. Chem. Int. Ed. Engl 1996, 35, 1155-1196; Angew. Chem. 1996, 108, 1242-1286. [11b] D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2828, and references cited therein. For some examples of cyclodextrin-based rotaxanes see: [11c] S. Anderson, T. D. W. Claridge, H. L. Anderson, Angew. Chem. Int. Ed. Engl. 1997, 36, 1310-1313; Angew. Chem 1997, 109, 1367-1370. - [11d] M. Born, H. Ritter, Angew. Chem. Int. Ed. Engl 1995, 34, 309-311; Angew. Chem. 1995, 107, 342-344.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 1310-1313
    • Anderson, S.1    Claridge, T.D.W.2    Anderson, H.L.3
  • 42
    • 0001691544 scopus 로고    scopus 로고
    • For reviews see: [11a] D. Philp, J. F. Stoddart, Angew. Chem. Int. Ed. Engl 1996, 35, 1155-1196; Angew. Chem. 1996, 108, 1242-1286. [11b] D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2828, and references cited therein. For some examples of cyclodextrin-based rotaxanes see: [11c] S. Anderson, T. D. W. Claridge, H. L. Anderson, Angew. Chem. Int. Ed. Engl. 1997, 36, 1310-1313; Angew. Chem 1997, 109, 1367-1370. - [11d] M. Born, H. Ritter, Angew. Chem. Int. Ed. Engl 1995, 34, 309-311; Angew. Chem. 1995, 107, 342-344.
    • (1997) Angew. Chem , vol.109 , pp. 1367-1370
  • 43
    • 33749139352 scopus 로고
    • For reviews see: [11a] D. Philp, J. F. Stoddart, Angew. Chem. Int. Ed. Engl 1996, 35, 1155-1196; Angew. Chem. 1996, 108, 1242-1286. [11b] D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2828, and references cited therein. For some examples of cyclodextrin-based rotaxanes see: [11c] S. Anderson, T. D. W. Claridge, H. L. Anderson, Angew. Chem. Int. Ed. Engl. 1997, 36, 1310-1313; Angew. Chem 1997, 109, 1367-1370. - [11d] M. Born, H. Ritter, Angew. Chem. Int. Ed. Engl 1995, 34, 309-311; Angew. Chem. 1995, 107, 342-344.
    • (1995) Angew. Chem. Int. Ed. Engl , vol.34 , pp. 309-311
    • Born, M.1    Ritter, H.2
  • 44
    • 0001252877 scopus 로고
    • For reviews see: [11a] D. Philp, J. F. Stoddart, Angew. Chem. Int. Ed. Engl 1996, 35, 1155-1196; Angew. Chem. 1996, 108, 1242-1286. [11b] D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725-2828, and references cited therein. For some examples of cyclodextrin-based rotaxanes see: [11c] S. Anderson, T. D. W. Claridge, H. L. Anderson, Angew. Chem. Int. Ed. Engl. 1997, 36, 1310-1313; Angew. Chem 1997, 109, 1367-1370. - [11d] M. Born, H. Ritter, Angew. Chem. Int. Ed. Engl 1995, 34, 309-311; Angew. Chem. 1995, 107, 342-344.
    • (1995) Angew. Chem. , vol.107 , pp. 342-344
  • 52
    • 0001805503 scopus 로고
    • [18a] D. J. Cram, Nature 1992, 356, 29-36.
    • (1992) Nature , vol.356 , pp. 29-36
    • Cram, D.J.1
  • 54
    • 33748327733 scopus 로고
    • [18b] D. J. Cram, M. E. Tanner, R. Thomas, Angew. Chem. Int. Ed. Engl. 1991, 30, 1024-1027; Angew Chem. 1991, 103, 1048-1051.
    • (1991) Angew Chem. , vol.103 , pp. 1048-1051
  • 56
    • 0030803420 scopus 로고    scopus 로고
    • [18c] R. Warmuth, Angew. Chem. Int. Ed. Engl. 1997, 36, 1347-1350; Angew. Chem. 1997, 109, 1406-1409.
    • (1997) Angew. Chem. , vol.109 , pp. 1406-1409
  • 67
    • 0031905296 scopus 로고    scopus 로고
    • [23d] P. Neri, A. Bottino, F. Cunsolo, M. Piattelli, E. Gavuzzo, Angew. Chem. Int. Ed. Engl. 1998, 37, 166-169; Angew. Chem 1998, 110, 175-178.
    • (1998) Angew. Chem , vol.110 , pp. 175-178
  • 69
    • 0025322535 scopus 로고
    • [24a] M. A. McKervey, M. Owens, H.-R. Schulten, W. Vogt, V. Böhmer, Angew. Chem. Int. Ed. Engl. 1990, 29, 280-282; Angew. Chem. 1990, 102, 326-328.
    • (1990) Angew. Chem. , vol.102 , pp. 326-328
  • 75
    • 0030820237 scopus 로고    scopus 로고
    • [24f] P. Schmitt, P. D. Beer, M. G. B. Drew, P. D. Sheen, Angew. Chem. Int. Ed. Engl. 1997, 36, 1840-1842; Angew Chem. 1997, 109, 1926-1928.
    • (1997) Angew Chem. , vol.109 , pp. 1926-1928
  • 78
    • 33748241554 scopus 로고
    • [25b] W. Wasikiwicz, G. Rokicki, J. Kielkiewicz, V. Böhmer, Angew. Chem. Int. Ed. Engl. 1994, 33, 214-216; Angew. Chem. 1994, 106, 230-232.
    • (1994) Angew. Chem. , vol.106 , pp. 230-232
  • 84
    • 0025893177 scopus 로고
    • A head-to-head calix[6]arene dimer was described by Shinkai et al., see: [30a] T. Arimura, S. Matsumoto, O. Teshima, T. Nagasaki, S. Shinkai, Tetrahedron Lett. 1991, 32, 5111-5114. The upper rim of a calix[4]arene was combined with the lower rim of a calix[8]arene by Pochini et al., see: [30b] A. Arduini, A. Pochini, A. Secchi, R. Ungaro, J. Chem. Soc., Chem. Commun. 1995, 879-880.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 5111-5114
    • Arimura, T.1    Matsumoto, S.2    Teshima, O.3    Nagasaki, T.4    Shinkai, S.5
  • 85
    • 37049067215 scopus 로고
    • A head-to-head calix[6]arene dimer was described by Shinkai et al., see: [30a] T. Arimura, S. Matsumoto, O. Teshima, T. Nagasaki, S. Shinkai, Tetrahedron Lett. 1991, 32, 5111-5114. The upper rim of a calix[4]arene was combined with the lower rim of a calix[8]arene by Pochini et al., see: [30b] A. Arduini, A. Pochini, A. Secchi, R. Ungaro, J. Chem. Soc., Chem. Commun. 1995, 879-880.
    • (1995) J. Chem. Soc., Chem. Commun. , pp. 879-880
    • Arduini, A.1    Pochini, A.2    Secchi, A.3    Ungaro, R.4
  • 91
    • 2742613728 scopus 로고    scopus 로고
    • Thesis, University of Nijmegen
    • [33b] F. Venema, Thesis, University of Nijmegen, 1996. -
    • (1996)
    • Venema, F.1
  • 93
    • 33746312419 scopus 로고
    • [34a] A. Collet, Tetrahedron 1987, 43, 5725-5759.
    • (1987) Tetrahedron , vol.43 , pp. 5725-5759
    • Collet, A.1
  • 95
    • 33749017578 scopus 로고
    • For some examples see: [35a] L. Garel, J.-P. Dutasta, A. Collet, Angew. Chem. Int. Ed. Engl. 1993, 32, 1169-1171; Angew. Chem. 1993, 105, 1249-1251. - [35b] J. Canceill, A. Collet, G. Gottarelli, P. Palmieri, J. Am Chem. Soc. 1987, 109, 6454-6464. - [35c] K. Bartik, M. Luhmer, J.-P. Dutaste, A. Collet, J. Reisse, J. Am. Chem. Soc. 1998, 120, 784-791.
    • (1993) Angew. Chem. Int. Ed. Engl. , vol.32 , pp. 1169-1171
    • Garel, L.1    Dutasta, J.-P.2    Collet, A.3
  • 96
    • 33749017578 scopus 로고
    • For some examples see: [35a] L. Garel, J.-P. Dutasta, A. Collet, Angew. Chem. Int. Ed. Engl. 1993, 32, 1169-1171; Angew. Chem. 1993, 105, 1249-1251. - [35b] J. Canceill, A. Collet, G. Gottarelli, P. Palmieri, J. Am Chem. Soc. 1987, 109, 6454-6464. - [35c] K. Bartik, M. Luhmer, J.-P. Dutaste, A. Collet, J. Reisse, J. Am. Chem. Soc. 1998, 120, 784-791.
    • (1993) Angew. Chem. , vol.105 , pp. 1249-1251
  • 97
    • 0000758990 scopus 로고
    • For some examples see: [35a] L. Garel, J.-P. Dutasta, A. Collet, Angew. Chem. Int. Ed. Engl. 1993, 32, 1169-1171; Angew. Chem. 1993, 105, 1249-1251. - [35b] J. Canceill, A. Collet, G. Gottarelli, P. Palmieri, J. Am Chem. Soc. 1987, 109, 6454-6464. - [35c] K. Bartik, M. Luhmer, J.-P. Dutaste, A. Collet, J. Reisse, J. Am. Chem. Soc. 1998, 120, 784-791.
    • (1987) J. Am Chem. Soc. , vol.109 , pp. 6454-6464
    • Canceill, J.1    Collet, A.2    Gottarelli, G.3    Palmieri, P.4
  • 98
    • 0032481407 scopus 로고    scopus 로고
    • For some examples see: [35a] L. Garel, J.-P. Dutasta, A. Collet, Angew. Chem. Int. Ed. Engl. 1993, 32, 1169-1171; Angew. Chem. 1993, 105, 1249-1251. - [35b] J. Canceill, A. Collet, G. Gottarelli, P. Palmieri, J. Am Chem. Soc. 1987, 109, 6454-6464. - [35c] K. Bartik, M. Luhmer, J.-P. Dutaste, A. Collet, J. Reisse, J. Am. Chem. Soc. 1998, 120, 784-791.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 784-791
    • Bartik, K.1    Luhmer, M.2    Dutaste, J.-P.3    Collet, A.4    Reisse, J.5
  • 105
    • 33748615619 scopus 로고
    • [37c] H. L. Anderson, A. Bashall, K. Henrick, M. McPartlin, J. K. M. Sanders, Angew. Chem Int. Ed. Engl. 1994, 33, 429-431; Angew. Chem. 1994, 106, 445-447.
    • (1994) Angew. Chem. , vol.106 , pp. 445-447
  • 107
    • 33748224376 scopus 로고
    • C. J. Walter, J. K. M. Sanders, Angew. Chem. Int. Ed. Engl. 1995, 34, 217-219; Angew. Chem. 1995, 107, 223-225.
    • (1995) Angew. Chem. , vol.107 , pp. 223-225
  • 111
    • 33748243226 scopus 로고
    • [39c] P. Timmerman, W. Verboom, F. C. J. M. Van Veggel, J. P. M. Van Duynhoven, D. N. Reinhoudt, Angew. Chem. Int. Ed. Engl. 1994, 33, 2345-2348; Angew. Chem 1994, 106, 2437-2440.
    • (1994) Angew. Chem , vol.106 , pp. 2437-2440
  • 115
    • 33748236521 scopus 로고
    • [41b] P. Timmerman, W. Verboom, F. C. J. M. Van Veggel, W. P. Van Hoorn, D. N. Reinhoudt, Angew. Chem. Int. Ed. Engl. 1994, 33, 1292-1295; Angew. Chem. 1994, 106, 1313-1315.
    • (1994) Angew. Chem. , vol.106 , pp. 1313-1315
  • 129
    • 0027531078 scopus 로고
    • [52b] A double porphyrin double calix[4]arene was reported by Weiss et al., see: Z. Asfari, J. Vicens, J. Weiss, Tetrahedron Lett. 1993, 34, 627-628. Reinhoudt et al. were unable to reproduce the procedure, see ref [53]
    • (1993) Tetrahedron Lett. , vol.34 , pp. 627-628
    • Asfari, Z.1    Vicens, J.2    Weiss, J.3
  • 148
    • 0000984691 scopus 로고
    • For some examples, see: [63a] M. Fujita, S. Nagao, K. Ogura, J. Am. Chem Soc. 1995, 117, 1649-1650. - [63b] C. A. Hunter, Angew. Chem. Int. Ed. Engl. 1995, 34, 1079-1081; Angew. Chem. 1995, 107, 1181-1183, and references cited therein. For a metal-coordinated assembly of two cavitands, see: [63b] P. Jacopozzi, E. Dalcanale, Angew. Chem. Int. Ed. Engl. 1997, 36, 613-615.
    • (1995) J. Am. Chem Soc. , vol.117 , pp. 1649-1650
    • Fujita, M.1    Nagao, S.2    Ogura, K.3
  • 149
    • 33748229364 scopus 로고
    • For some examples, see: [63a] M. Fujita, S. Nagao, K. Ogura, J. Am. Chem Soc. 1995, 117, 1649-1650. - [63b] C. A. Hunter, Angew. Chem. Int. Ed. Engl. 1995, 34, 1079-1081; Angew. Chem. 1995, 107, 1181-1183, and references cited therein. For a metal-coordinated assembly of two cavitands, see: [63b] P. Jacopozzi, E. Dalcanale, Angew. Chem. Int. Ed. Engl. 1997, 36, 613-615.
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.34 , pp. 1079-1081
    • Hunter, C.A.1
  • 150
    • 0000984691 scopus 로고
    • and references cited therein.
    • For some examples, see: [63a] M. Fujita, S. Nagao, K. Ogura, J. Am. Chem Soc. 1995, 117, 1649-1650. - [63b] C. A. Hunter, Angew. Chem. Int. Ed. Engl. 1995, 34, 1079-1081; Angew. Chem. 1995, 107, 1181-1183, and references cited therein. For a metal-coordinated assembly of two cavitands, see: [63b] P. Jacopozzi, E. Dalcanale, Angew. Chem. Int. Ed. Engl. 1997, 36, 613-615.
    • (1995) Angew. Chem. , vol.107 , pp. 1181-1183
  • 153
    • 0029838574 scopus 로고    scopus 로고
    • [64a] B. C. Hamann, K. D Shimizu, J. Rebek, Jr., Angew. Chem Int. Ed. Engl. 1996, 35, 1326-1329; Angew. Chem. 1996, 108, 1425-1427.-
    • (1996) Angew. Chem. , vol.108 , pp. 1425-1427
  • 161
    • 2742604848 scopus 로고
    • Thesis, University of Twente
    • [68b] R. H. Vreekamp, Thesis, University of Twente, 1995.
    • (1995)
    • Vreekamp, R.H.1
  • 167
    • 0029791247 scopus 로고    scopus 로고
    • [73a] R. H. Vreekamp, J. P. M. Van Duynhoven, M. Hubert, W. Verboom, D. N. Reinhoudt, Angew. Chem. Int. Ed Engl. 1996, 35, 1215-1218; Angew. Chem. 1996, 108, 1306-1309.
    • (1996) Angew. Chem. , vol.108 , pp. 1306-1309
  • 170
    • 0030968810 scopus 로고    scopus 로고
    • [74a] w. T. s. Huck, R. Hulst, P. Timmerman, F. C. J. M. Van Veggel, D. N. Reinhoudt, Angew. Chem. Int. Ed. Engl 1997, 36, 1006-1008; Angew. Chem. 1997, 109, 1046-1049.
    • (1997) Angew. Chem. , vol.109 , pp. 1046-1049
  • 171
    • 2742538923 scopus 로고
    • Thesis, University of Twente
    • [74b] W. T. S. Huck, Thesis, University of Twente. 1995.
    • (1995)
    • Huck, W.T.S.1
  • 173
    • 2742580493 scopus 로고    scopus 로고
    • Thesis, University of British Columbia
    • [75b] R. G. Chapman, Thesis, University of British Columbia, 1997.
    • (1997)
    • Chapman, R.G.1


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