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1
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12044260020
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For cation-π interaction of quaternary ammonium compounds with electron-rich guest compounds see
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For cation-π interaction of quaternary ammonium compounds with electron-rich guest compounds see: a) P. C. Kearney, L. S. Mizoue, R. A. Kumpf, J. E. Forman, A. McCurdy, D. A. Dougherty, J. Am. Chem. Soc. 1993, 115, 9907-9919;
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Kearney, P.C.1
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McCurdy, A.5
Dougherty, D.A.6
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2
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33845278120
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b) M. A. Petti, T. J. Shepodd, R. E. Barrans, Jr., D. A. Dougherty, ibid. 1988, 110, 6825-6840;
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Petti, M.A.1
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Barrans Jr., R.E.3
Dougherty, D.A.4
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4
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0003461218
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(Eds.: J. L. Atwood, J. E. D. Davies, D. D. McNicol, F. Vögtle), Pergamon Elsevier, Oxford
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d) D. A. Dougherty, Comprehensive Supramolecular Chemistry, Vol. 2 (Eds.: J. L. Atwood, J. E. D. Davies, D. D. McNicol, F. Vögtle), Pergamon Elsevier, Oxford, 1996.
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Dougherty, D.A.1
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5
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0028216095
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For the inclusion of uncharged molecules in cage compounds see
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For the inclusion of uncharged molecules in cage compounds see: T. A. Robbins, C. B. Knobler, D. R. Bellew, D. J. Cram, J. Am. Chem. Soc. 1994, 116, 111-122;
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Robbins, T.A.1
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6
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0001805503
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review
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review: D. J. Cram, Nature 1992, 356, 29-36.
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Nature
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Cram, D.J.1
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7
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33845378004
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Examples of silver π-prismands and π-spherands
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Examples of silver π-prismands and π-spherands: a) H. C. Kang, A. W. Hanson, B. Eaton, V. Boekelheide, J. Am. Chem. Soc. 1985, 107, 1979-1985;
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Kang, H.C.1
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8
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33845557895
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b) J.-L. Pierre, P. Baret, P. Chautemps, M. Armand, ibid. 1981, 103, 2986-2988;
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Pierre, J.-L.1
Baret, P.2
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9
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0001573508
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C. Cohen-Addad, P. Baret, P. Chautemps, J.-L. Pierre, Acta Crystallogr. Sect. C 1983, 39, 1346-1349;
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Acta Crystallogr. Sect. C
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Cohen-Addad, C.1
Baret, P.2
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Pierre, J.-L.4
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10
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0000668048
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c) J. E. McMurry, G. J. Harley, J. R. Matz, J. C. Clardy, J. Mitchell, J. Am. Chem. Soc. 1986, 108, 515-516;
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McMurry, J.E.1
Harley, G.J.2
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Mitchell, J.5
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11
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0346636493
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d) H. Schmidbaur, W. Bublak, B. Huber, G. Reber, G. Müller, Angew. Chem. 1986, 98, 1108-1109;
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Schmidbaur, H.1
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13
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0345598322
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For further examples of π-donor participation in complexation of silver ions, see
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For further examples of π-donor participation in complexation of silver ions, see: A. Ikeda, S. Shinkai, J. Am. Chem. Soc. 1994, 116, 3102-3110;
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Ikeda, A.1
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0012822015
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H. Schmidbaur, R. Hager, B. Huber, G. Müller, Angew. Chem. 1987, 99, 354-356;
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Schmidbaur, H.1
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17
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84985740884
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b) C. Elschenbroich, J. Schneider, M. Wünsch, J.-L. Pierre, P. Baret, P. Chautemps, Chem. Ber. 1988, 121, 177-183.
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Elschenbroich, C.1
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Baret, P.5
Chautemps, P.6
-
18
-
-
0001615190
-
-
Another class of spherical hydrocarbons based on cavitands has been proposed by Cram
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Another class of spherical hydrocarbons based on cavitands has been proposed by Cram: a) D. J. Cram, Science 1983, 219, 1177-1183;
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Science
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Cram, D.J.1
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19
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0003461218
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(Eds.: J. L. Atwood, J. E. D. Davies, D. D. McNicol, F. Vögtle), Pergamon Elsevier, Oxford
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b) E. Maverick, D. J. Cram, Comprehensive Supramolecular Chemistry, Vol. 2 (Eds.: J. L. Atwood, J. E. D. Davies, D. D. McNicol, F. Vögtle), Pergamon Elsevier, Oxford, 1996.
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Maverick, E.1
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20
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0027786691
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and references therein
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R. Taylor, G. J. Langley, H. W. Kroto, D. R. M. Walton, Nature (London) 1993, 366, 728-731, and references therein;
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Nature (London)
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Taylor, R.1
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21
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0028803144
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b) C. Crowley, H. W. Kroto, R. Taylor, D. R. M. Walton, M. S. Bratcher, P.-C. Cheng, L. T. Scott, Tetrahedron Lett. 1995, 36, 9215-9218;
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Crowley, C.1
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22
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0029874522
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c) J. Osterodt, A. Zett, F. Vögtle, Tetrahedron 1996, 52, 4949-4962.
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Tetrahedron
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Osterodt, J.1
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24
-
-
33748240904
-
-
and references therein
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Angew. Chem. Int. Ed. Engl. 1995, 34, 981-985, and references therein.
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Angew. Chem. Int. Ed. Engl.
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-
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25
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84891539553
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J. Gross, C. Seel, F. Vögtle, Angew. Chem. 1992, 104, 112-113;
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Angew. Chem.
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Gross, J.1
Seel, C.2
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27
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84891515436
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J. Gross, G. Harder, F. Vögtle, H. Stephan, K. Gloe, Angew. Chem. 1995, 107, 521-524;
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Gross, J.1
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29
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0001125356
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24) has been calculated in the light of conjugation
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24) has been calculated in the light of conjugation: O. Wennerström, U. Noriander, J. Phys. Chem. 1985, 89, 3233-3237;
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Wennerström, O.1
Noriander, U.2
-
30
-
-
0028400836
-
-
recently electronic structures of conjugated "spheriphanes" have been discussed
-
recently electronic structures of conjugated "spheriphanes" have been discussed: P. W. Fowler, S. J. Austin, J. Chem. Inf. Comput. Sci. 1994, 34, 264-269.
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J. Chem. Inf. Comput. Sci.
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Fowler, P.W.1
Austin, S.J.2
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34
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0003559584
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Wiley, Chichester
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Cyclophane Chemistry, Wiley, Chichester 1993.
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(1993)
Cyclophane Chemistry
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35
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0002712411
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P. Knops, N. Sendhoff, H.-B. Mekelburger, F. Vögtle, Top. Curr. Chem. 1992, 161, 1-36.
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Top. Curr. Chem.
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Knops, P.1
Sendhoff, N.2
Mekelburger, H.-B.3
Vögtle, F.4
-
37
-
-
84891540426
-
-
note
-
36 can be obtained directly from the hexabromide 13 by cyclization with phenyllithium because of its rigid spacers, an alternative procedure that proved to be unsuccessful in the case of the other more flexible cyclization precursors.
-
-
-
-
40
-
-
0347502012
-
-
3/benzene adduct of a spheriphane that has three ethane linkages substituted by oxomethylene moieties, see
-
3/benzene adduct of a spheriphane that has three ethane linkages substituted by oxomethylene moieties, see: H. B. Mekelburger, J. Gross, J. Schmitz, M. Nieger, F. Vögtle, Chem. Ber. 1993, 126, 1713-1721.
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Chem. Ber.
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Mekelburger, H.B.1
Gross, J.2
Schmitz, J.3
Nieger, M.4
Vögtle, F.5
-
41
-
-
84891502916
-
-
note
-
Full geometry optimization was performed by PM3 at the RHF-SCF level (Mopac 6.0, QCPE 455).
-
-
-
-
43
-
-
84891537673
-
-
note
-
The NMR spectra of an endohedral complex should be more simple than that of an exohedral one because of the higher symmetry.
-
-
-
-
45
-
-
84891540183
-
-
note
-
A complex of 1:1 stoichiometry is present if the graph in Fig. 7 has a slope of one.
-
-
-
-
46
-
-
0347502012
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-
B. Mekelburger, J. Gross, J. Schmitz, M. Nieger, F. Vögtle, Chem. Ber. 1993, 126, 1713-1721.
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Chem. Ber.
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Mekelburger, B.1
Gross, J.2
Schmitz, J.3
Nieger, M.4
Vögtle, F.5
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47
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0001647167
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(Eds.: G. M. Sheldrick, C. Krüger and R. Goddard), Oxford University Press, Oxford
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G. M. Sheldrick in Crystallographic Computing 3 (Eds.: G. M. Sheldrick, C. Krüger and R. Goddard), Oxford University Press, Oxford, 1985, 175-189.
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Crystallographic Computing 3
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Sheldrick, G.M.1
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48
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0004264855
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Chemical Crystallography Laboratory, Oxford
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D. Watkin, J. R. Carruthers, P. W. Betteridge, CRYSTALS, Chemical Crystallography Laboratory, Oxford, 1990.
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(1990)
CRYSTALS
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Watkin, D.1
Carruthers, J.R.2
Betteridge, P.W.3
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49
-
-
84891499585
-
-
note
-
Crystallographic data (excluding structure factors) for the structure reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-1220-36. Copies of the data can be obtained free of charge on application to the Director, CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (Fax: Int. code +(1223)336-033; e-mail: teched@chemcrys.cam.ac.uk).
-
-
-
-
51
-
-
84891507015
-
-
note
-
We shall not report here the NMR spectra, which are complex as the product is a mixture of isomers.
-
-
-
-
52
-
-
84891519633
-
-
note
-
-6 mbar is necessary.
-
-
-
-
53
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84982401577
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F. Vögtle, M. Zuber, R. G. Lichtenthaler, Chem. Ber. 1973, 106, 717-718.
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Chem. Ber.
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Vögtle, F.1
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0001670299
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F. Vögtle, J. Schmitz, M. Nieger, Chem. Ber. 1992, 125, 2523-2525.
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Chem. Ber.
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Vögtle, F.1
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0004014601
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Springer, Berlin, Heidelberg, New York
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K. Cammann, Das Arbeiten mit Ionenselektiven Elektroden, Springer, Berlin, Heidelberg, New York, 1996.
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Das Arbeiten Mit Ionenselektiven Elektroden
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Cammann, K.1
|