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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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(1997)
Angew. Chem. Int. Ed. Engl.
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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.
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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.
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(1996)
Angew. Chem. Int. Ed. Engl.
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Sauvage, J.-P.4
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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.
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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.
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(1996)
Angew. Chem. Int. Ed. Engl.
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Hasenknopf, B.1
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Baum, G.4
Fenske, D.5
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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.
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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.
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Lehn, J.-M.2
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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.
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Angew. Chem.
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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.
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, vol.36
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Hanan, G.S.1
Volkmer, D.2
Schubert, U.S.3
Lehn, J.-M.4
Baum, G.5
Fenske, D.6
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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.
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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.
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