-
3
-
-
0003837875
-
-
V. Balzani, L. De Cola, (Eds.), Kluwer, Dordrecht
-
c) F. Diederich, Supramolecular Chemistry, V. Balzani, L. De Cola, (Eds.), Kluwer, Dordrecht 1992.
-
(1992)
Supramolecular Chemistry
-
-
Diederich, F.1
-
6
-
-
4243468938
-
-
and references cited therein
-
J. C. Ma, D. A. Dougherty, Chem. Rev. 1997, 97, 1303 and references cited therein.
-
(1997)
Chem. Rev.
, vol.97
, pp. 1303
-
-
Ma, J.C.1
Dougherty, D.A.2
-
10
-
-
0025878347
-
-
d) C. A. Hunter, J. Singh, J. M. Thornton, J. Mol. Biol. 1991, 218, 837;
-
(1991)
J. Mol. Biol.
, vol.218
, pp. 837
-
-
Hunter, C.A.1
Singh, J.2
Thornton, J.M.3
-
12
-
-
0004146786
-
-
The Royal Society of Chemistry, Cambridge
-
a) C. D. Gutsche, Calixarenes, The Royal Society of Chemistry, Cambridge 1989;
-
(1989)
Calixarenes
-
-
Gutsche, C.D.1
-
13
-
-
0003825877
-
-
The Royal Society of Chemistry, Cambridge
-
b) F. Diederich, Cyclophanes, The Royal Society of Chemistry, Cambridge 1991;
-
(1991)
Cyclophanes
-
-
Diederich, F.1
-
16
-
-
0347746898
-
-
Elsevier, London
-
d) J. L. Atwood, J. E. D. Davies, D. D. MacNicol, F. Vögtle (Eds.), Comprehensive Supra-molecular Chemistry, Elsevier, London 1996.
-
(1996)
Comprehensive Supra-molecular Chemistry
-
-
Atwood, J.L.1
Davies, J.E.D.2
MacNicol, D.D.3
Vögtle, F.4
-
18
-
-
0001301147
-
-
b) J. Rebek Jr., Angew. Chem. 1990, 102, 261; Angew. Chem. Int. Ed. Engl. 1990, 29, 245;
-
(1990)
Angew. Chem.
, vol.102
, pp. 261
-
-
Rebek Jr., J.1
-
19
-
-
0025290381
-
-
b) J. Rebek Jr., Angew. Chem. 1990, 102, 261; Angew. Chem. Int. Ed. Engl. 1990, 29, 245;
-
(1990)
Angew. Chem. Int. Ed. Engl.
, vol.29
, pp. 245
-
-
-
20
-
-
84989442640
-
-
c) R. Güther, M. Nieger, K. Rissanen, F. Vögtle, Chem. Ber. 1994, 127, 743;
-
(1994)
Chem. Ber.
, vol.127
, pp. 743
-
-
Güther, R.1
Nieger, M.2
Rissanen, K.3
Vögtle, F.4
-
24
-
-
25744459223
-
-
in print
-
a) F.-G. Klärner, U. Burkert, M. Kamieth, R. Boese, J. Benet-Buchholz, Chem. Eur. J. 1999, 5, in print,
-
(1999)
Chem. Eur. J.
, vol.5
-
-
Klärner, F.-G.1
Burkert, U.2
Kamieth, M.3
Boese, R.4
Benet-Buchholz, J.5
-
25
-
-
0001273215
-
-
b) F.-G. Klärner, J. Benkhoff, R. Boese, U. Burkert, M. Kamieth, U. Naatz, Angew. Chem. 1996, 108, 1195; Angew. Chem. Int. Ed. Engl. 1996, 35, 1130.
-
(1996)
Angew. Chem.
, vol.108
, pp. 1195
-
-
Klärner, F.-G.1
Benkhoff, J.2
Boese, R.3
Burkert, U.4
Kamieth, M.5
Naatz, U.6
-
26
-
-
0029811414
-
-
b) F.-G. Klärner, J. Benkhoff, R. Boese, U. Burkert, M. Kamieth, U. Naatz, Angew. Chem. 1996, 108, 1195; Angew. Chem. Int. Ed. Engl. 1996, 35, 1130.
-
(1996)
Angew. Chem. Int. Ed. Engl.
, vol.35
, pp. 1130
-
-
-
27
-
-
84988097442
-
-
a) F. Vögtle, M. Händel, S. Meier, S. Ottens-Hildebrandt, F. Ott, T. Schmidt, Liebigs Ann. 1995, 739;
-
(1995)
Liebigs Ann.
, pp. 739
-
-
Vögtle, F.1
Händel, M.2
Meier, S.3
Ottens-Hildebrandt, S.4
Ott, F.5
Schmidt, T.6
-
28
-
-
0039405121
-
-
b) T. Dünnwald, R. Jäger, F. Vögtle, Chem. Eur. J. 1997, 3, 2043;
-
(1997)
Chem. Eur. J.
, vol.3
, pp. 2043
-
-
Dünnwald, T.1
Jäger, R.2
Vögtle, F.3
-
29
-
-
0000633029
-
-
c) D. Philip, J. F. Stoddart, Angew. Chem. 1996, 108, 1242; Angew. Chem. Int. Ed. Engl. 1996, 35, 1155;
-
(1996)
Angew. Chem.
, vol.108
, pp. 1242
-
-
Philip, D.1
Stoddart, J.F.2
-
30
-
-
17344372922
-
-
c) D. Philip, J. F. Stoddart, Angew. Chem. 1996, 108, 1242; Angew. Chem. Int. Ed. Engl. 1996, 35, 1155;
-
(1996)
Angew. Chem. Int. Ed. Engl.
, vol.35
, pp. 1155
-
-
-
32
-
-
0001220128
-
-
M. Kamieth, F.-G. Klärner, F. Diederich, Angew. Chem. 1998, 110, 3497; Angew. Chem. Int. Ed. Engl. 1998, 37, 3300.
-
(1998)
Angew. Chem.
, vol.110
, pp. 3497
-
-
Kamieth, M.1
Klärner, F.-G.2
Diederich, F.3
-
33
-
-
0032542332
-
-
M. Kamieth, F.-G. Klärner, F. Diederich, Angew. Chem. 1998, 110, 3497; Angew. Chem. Int. Ed. Engl. 1998, 37, 3300.
-
(1998)
Angew. Chem. Int. Ed. Engl.
, vol.37
, pp. 3300
-
-
-
34
-
-
0346486202
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For the nonlinear regression analyses of the titration data we used the computer programs TITRATOR, M. Kamieth, Dissertation, Universität GH Essen 1998, and ASSOCIATE, B. Peterson, Ph.D. Dissertation, University of California at Los Angeles 1994. We thank Prof. Dr. F. Diederich for providing us with a copy of the ASSOCIATE program
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For the nonlinear regression analyses of the titration data we used the computer programs TITRATOR, M. Kamieth, Dissertation, Universität GH Essen 1998, and ASSOCIATE, B. Peterson, Ph.D. Dissertation, University of California at Los Angeles 1994. We thank Prof. Dr. F. Diederich for providing us with a copy of the ASSOCIATE program.
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35
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0037808071
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For the synthesis of pseudorotaxanes with secondary dialkyl-ammonium salts and crown ethers see: P. R. Ashton, E. J. T. Chrystal, P. T. Glink, S. Menzer, C. Schiano, N. Spencer, J. F. Stoddart, P. A. Tasker, A. J. P. White, D. J. Williams, Chem. Eur. J. 1996, 2, 709.
-
(1996)
Chem. Eur. J.
, vol.2
, pp. 709
-
-
Ashton, P.R.1
Chrystal, E.J.T.2
Glink, P.T.3
Menzer, S.4
Schiano, C.5
Spencer, N.6
Stoddart, J.F.7
Tasker, P.A.8
White, A.J.P.9
Williams, D.J.10
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36
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0347746896
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This finding is in good agreements with molecular mechanics calculations (AMBER*). In the calculated energetic minimum structure of complex 3@1a the nitrogen atom is centered in the cavity of 1a
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This finding is in good agreements with molecular mechanics calculations (AMBER*). In the calculated energetic minimum structure of complex 3@1a the nitrogen atom is centered in the cavity of 1a.
-
-
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37
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0345855341
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At room temperature all complexation/decomplexation processes are fast with respect to the NMR time scale so that only averaged signals of complexed and free substrate are observed
-
At room temperature all complexation/decomplexation processes are fast with respect to the NMR time scale so that only averaged signals of complexed and free substrate are observed.
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38
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0347746893
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2 group adjacent to the oxygen in the reactand 9 (t, 3.50 ppm) and the product 11 (t, 4.42 ppm)
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2 group adjacent to the oxygen in the reactand 9 (t, 3.50 ppm) and the product 11 (t, 4.42 ppm).
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40
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0347746894
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We assume that the orange precipitate obtained from the mixture of the solutions of 1a and 12 consists of the clipped rotaxane 12@1a. But up to now we have not been able to grow crystals suitable for a crystal stucture analysis
-
a) We assume that the orange precipitate obtained from the mixture of the solutions of 1a and 12 consists of the clipped rotaxane 12@1a. But up to now we have not been able to grow crystals suitable for a crystal stucture analysis.
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41
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0347746895
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M. Kamieth, F.-G. Klärner, to be published
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b) M. Kamieth, F.-G. Klärner, to be published.
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-
-
-
45
-
-
33947338588
-
-
a) J. M. Bollinger, M. B. Comisarov, C. A. Cupas, G. A. Olah, J. Am. Chem. Soc. 1967, 89, 5687;
-
(1967)
J. Am. Chem. Soc.
, vol.89
, pp. 5687
-
-
Bollinger, J.M.1
Comisarov, M.B.2
Cupas, C.A.3
Olah, G.A.4
-
47
-
-
84986437005
-
-
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.
-
(1990)
J. Comput. Chem.
, vol.11
, pp. 440
-
-
Mohamadi, F.1
Richards, N.G.I.2
Guida, W.C.3
Liskamp, R.4
Lipton, M.5
Chang, G.6
Hendrickson, T.7
Still, W.C.8
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