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4544265430
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note
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The molecular parameters of 1a, as estimated by CPK molecular modeling, is ≈ 5 × 1 nm.
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63
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33748668687
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note
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1b-d are not soluble in the mixed solvent of p-xylene and 1-propanol but form precipitates. From this fact, it is reasonable to deduce that 1a-d coassemble to form gels.
-
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68
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4544240516
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note
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donor.
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70
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4544270466
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note
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As one of the referees pointed out, the suggested coassembly of 1a-d should lead to assemblies with a random distribution of the four units, and consequently many different decay pathways are likely to exist, instead of a "clean" decay channel to the lowest energy state of 1d.
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71
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4544223747
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note
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We have found that when N,N′-di-n-butyl-1,7 -bis(4-tert-butyl- phenoxy)-3,4,9,10-perylenetetracarboxylic diimide (compound 4 without the cholesterol group shown in the Supporting Information) was added as an energy acceptor, emission from 4 was not intensified as for 1b. This result further supports the view that the structural similarity of the perylene-cholesterol conjugates 1a-d plays an important role in coassembling acceptors and mediating efficient energy transfer.[18]
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72
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0042027187
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K. J. C. van Bommel, A. Friggeri, S. Shinkai, Angew. Chem. 2003, 115, 1010-1030; Angew. Chem. Int. Ed. 2003, 42, 980-999.
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Van Bommel, K.J.C.1
Friggeri, A.2
Shinkai, S.3
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73
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K. J. C. van Bommel, A. Friggeri, S. Shinkai, Angew. Chem. 2003, 115, 1010-1030; Angew. Chem. Int. Ed. 2003, 42, 980-999.
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74
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Cholesterol-based perylene derivatives were synthesized according to the following references: a) H. Quante, P. Schlichting, U. Rohr, Y. Geerts, K. Müllen, Macromol. Chem. Phys. 1996, 197, 4029-4044;
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(1996)
Macromol. Chem. Phys.
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Quante, H.1
Schlichting, P.2
Rohr, U.3
Geerts, Y.4
Müllen, K.5
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75
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0035909167
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b) T. Ishii, R. Iguchi, E. Snip, M. Ikeda, S. Shinkai, Langmuir 2001, 17, 5825-5833;
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(2001)
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Ishii, T.1
Iguchi, R.2
Snip, E.3
Ikeda, M.4
Shinkai, S.5
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76
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4544365549
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US Pat. 6,184,378, 2001
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c) A. Böhm, H. Arms, G. Henning, P. Blaschka, US Pat. 6,184,378, 2001;
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Böhm, A.1
Arms, H.2
Henning, G.3
Blaschka, P.4
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