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The Royal Society of Chemistry, Cambridge
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b) F. Diederich, Cyclophanes, The Royal Society of Chemistry, Cambridge, 1994;
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Cyclophanes
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0001128585
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a) M. M. Conn, G. Deslongchamps, J. de Mendoza, J. Rebek, Jr., J. Am. Chem. Soc. 1993, 115, 3548-3557;
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0000687913
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b) L. F. Newcomb, T. S. Haque, S. H. Gellmann, J. Am. Chem. Soc. 1995, 111, 6509-6519.
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0030018635
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b) T. Z. Mondasini-Denti, W. F. Van Gunsteren, F. Diederich, J. Am. Chem. Soc. 1996, 118, 6044-6051.
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Van Gunsteren, W.F.2
Diederich, F.3
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12
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0001522501
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simplified by M. Kamieth, Diplomarbeit, Universität GH Essen
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Compound 6 can be obtained from indene in four steps according to D. N. Butler, R. A. Snow, Can. J. Chem. 1975, 53, 256-262 (simplified by M. Kamieth, Diplomarbeit, Universität GH Essen, 1995).
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Butler, D.N.1
Snow, R.A.2
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0001273215
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F.-G. Klärner, J. Benkhoff, R. Boese, U. Burkert, M. Kamieth, U. Naatz, Angew. Chem. 1996, 108, 1195-1198; Angew. Chem. Int. Ed. Engl. 1996, 35, 1130-1133.
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Klärner, F.-G.1
Benkhoff, J.2
Boese, R.3
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Kamieth, M.5
Naatz, U.6
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14
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0029811414
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F.-G. Klärner, J. Benkhoff, R. Boese, U. Burkert, M. Kamieth, U. Naatz, Angew. Chem. 1996, 108, 1195-1198; Angew. Chem. Int. Ed. Engl. 1996, 35, 1130-1133.
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15
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85034558893
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note
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We thank Dr. A. E. Wigger who assisted in working out the procedure of the synthesis of 10a.
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-
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16
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85034544259
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For nonlinear regression analysis of the titration data we used the program Associate V 1.6, B. Peterson, Ph. D. Dissertation, University of California at Los Angeles, 1994. We thank Professor F. Diederich for providing us with a copy of the program
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For nonlinear regression analysis of the titration data we used the program Associate V 1.6, B. Peterson, Ph. D. Dissertation, University of California at Los Angeles, 1994. We thank Professor F. Diederich for providing us with a copy of the program.
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17
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33751552981
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D. A. Stauffer, R. E. Barrans, D. A. Dougherty, J. Org. Chem. 1990, 55, 2762-2767.
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Stauffer, D.A.1
Barrans, R.E.2
Dougherty, D.A.3
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19
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0002024340
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F. Diederich, D. B. Smithrud, E. M. Sanford, T. B. Wyman, S. B. Fergusson, D. B. Caranague, I. Chao, K. N. Houk, Acta Chem. Scand. 1992, 46, 205-215.
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Diederich, F.1
Smithrud, D.B.2
Sanford, E.M.3
Wyman, T.B.4
Fergusson, S.B.5
Caranague, D.B.6
Chao, I.7
Houk, K.N.8
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20
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84986437005
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All molecular mechanics calculations were performed with the AMBER* forcefield implemented in the molecular modeling package MacroModel 5.0: F. Mohamadi, N. G. I. Richards, W. C. Guida, R. Liskamp, M. Lipton, G. Chang, T. Hendrickson, W. C. Still, J. Comput. Chem. 1990, 11, 440-467. The quantum chemical calculations were performed with the semiempirical AM1 method implemented in the program SPARTAN 4.0; Wavefunction, 18401 Von Karman, Suite 370, Irvine, California 92715 (USA).
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Mohamadi, F.1
Richards, N.G.I.2
Guida, W.C.3
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Lipton, M.5
Chang, G.6
Hendrickson, T.7
Still, W.C.8
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21
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85034554172
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note
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As a criterion for the expansion of the tweezer molecules we use the averaged distance between the opposing terminal C-C bonds of the tips of the tweezer.
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22
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0001220128
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F.-G. Klärner, M. Kamieth, F. Diederich, Angew. Chem. 1998, 110, 3497-3500; Angew. Chem. Int. Ed. 1998, 37, 3303-3306.
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Angew. Chem.
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Klärner, F.-G.1
Kamieth, M.2
Diederich, F.3
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23
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0032542276
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F.-G. Klärner, M. Kamieth, F. Diederich, Angew. Chem. 1998, 110, 3497-3500; Angew. Chem. Int. Ed. 1998, 37, 3303-3306.
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24
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0000453561
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a) M. Luhmer, K. Bartik, A. Dejaegere, P. Bovy, J. Riesse, Bull. Soc. Chim. Fr. 1994, 131, 603-606;
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Luhmer, M.1
Bartik, K.2
Dejaegere, A.3
Bovy, P.4
Riesse, J.5
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