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Knaapila, M.1
Garamus, V.M.2
Dias, F.B.3
Almásy, L.4
Galbrecht, F.5
Charas, A.6
Morgado, J.7
Burrows, H.D.8
Scherf, U.9
Monkman, A.P.10
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67
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47349125910
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We have not determined the gelator solubility of our compounds, see: A. R. Hirst, I. A. Coates, T. R. Boucheteau, J. F. Miravet, B. Escuder, V. Castelleto, I. W. Hamley, D. K. Smith, J. Am. Chem. Soc. 2008,130, 9113.
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Hirst, A.R.1
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Boucheteau, T.R.3
Miravet, J.F.4
Escuder, B.5
Castelleto, V.6
Hamley, I.W.7
Smith, D.K.8
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68
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70450129726
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In contrast, no LD but strong CD effects were found in aggregated and partially precipitated solutions of 2, 3 and 4
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In contrast, no LD but strong CD effects were found in aggregated and partially precipitated solutions of 2, 3 and 4.
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69
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33750959398
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H. Cheun, F. Galbrecht, B. S. Nehls, U. Scherf, M. J. Winokur, J. Lumin. 2007,122-123, 212.
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Cheun, H.1
Galbrecht, F.2
Nehls, B.S.3
Scherf, U.4
Winokur, M.J.5
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70
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70450135399
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At present, our results do not allow us to distinguish whether aggregation is induced by the conformational changes or vice versa
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At present, our results do not allow us to distinguish whether aggregation is induced by the conformational changes or vice versa.
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71
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0033663651
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a) S. Boileau, L. Bouteiller, F. Lauprêtre, F. Lortie, New J. Chem. 2000, 24, 845;
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Boileau, S.1
Bouteiller, L.2
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Lortie, F.4
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b) Y. Liu, Y. Li, L. Jiang, H. Gan, H. Liu, Y. Li, J. Zhuang, F. Lu, D. Zhu, J. Org. Chem. 2004, 69, 9049.
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Liu, Y.1
Li, Y.2
Jiang, L.3
Gan, H.4
Liu, H.5
Li, Y.6
Zhuang, J.7
Lu, F.8
Zhu, D.9
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73
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70450143096
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As the models most frequently used to describe self-assembly (isodesmic and cooperative model) both assume thermodynamically controlled processes, our data do not allow application of these models
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As the models most frequently used to describe self-assembly (isodesmic and cooperative model) both assume thermodynamically controlled processes, our data do not allow application of these models.
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74
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70450152309
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In contrast, the three compounds 2, 3 and 4 gave aggregates that resembled crystallite structures, in line with their inability to form organogels
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In contrast, the three compounds 2, 3 and 4 gave aggregates that resembled crystallite structures, in line with their inability to form organogels.
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75
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0035964514
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S. Y. Hong, D. K. Kim, C. Y. Kim, R. Hoffmann, Macromolecules 2001, 34, 6474.
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Hong, S.Y.1
Kim, D.K.2
Kim, C.Y.3
Hoffmann, R.4
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76
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70450124169
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Interestingly, the formation of the flipped configuration is favoured by the presence of hydrogen bonds rather than the "shifted" conformation, which is more stable in poly(dioctylfluorene) (see ref. [18b])
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Interestingly, the formation of the flipped configuration is favoured by the presence of hydrogen bonds rather than the "shifted" conformation, which is more stable in poly(dioctylfluorene) (see ref. [18b]).
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