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Application of 1,3,4-oxadiazole derivatives in electroluminescent devices: Y. Hamada, C. Adachi, T. Tsutsui and S. Saito, Jpn. J. Appl. Phys., 1992, 31, 1812; A. R. Brown, D. D. C. Bradley, J. H. Burroughes, R. H. Friend, N. C. Greenham, P. L. Burn, A. B. Holmes and A. Kraft, Appl. Phys. Lett., 1992, 61, 2793.
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For other syntheses of poly(aramide)s by palladium-catalysed carbonylations, see M. Yoneyama, M. Kakimoto and Y. Imai, Macromolecules, 1988, 21, 1908; S. R. Turner, R. J. Perry and R. W. Blevins, Macromolecules, 1992, 25, 4819; V. R. Reichert and L. J. Mathias, Macromolecules, 1994, 27, 7024.
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Until now, dendrimer-dendrimer interactions involved mainly micelle formation, aggregation or self-assembly in solution, and liquid-crystalline phase transition in the absence of solvent: G. R. Newkome, C. N. Moorefield, G. R. Baker, R. K. Behera, G. H. Escamillia and M. J. Saunders, Angew. Chem., Int. Ed. Engl., 1992, 31, 917; J. M. J. Fréchet and I. Gitsov, Macromol. Symp., 1995, 98, 441; V. Percec, P. Chu, G. Ungar and J. Zhou, J. Am. Chem. Soc., 1995, 117, 11441; J. C. M. van Hest, D. A. P. Delnoye, M. W. P. L. Baars, C. Elissen-Román, M. H. P. van Genderen and E. W. Meijer, Chem. Eur. J., 1996, 2, 1616; S. C. Zimmerman, F. Zeng, D. E. C. Reichert and S. V. Kolotuchin, Science, 1996, 271, 1095.
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Behera, R.K.4
Escamillia, G.H.5
Saunders, M.J.6
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Until now, dendrimer-dendrimer interactions involved mainly micelle formation, aggregation or self-assembly in solution, and liquid-crystalline phase transition in the absence of solvent: G. R. Newkome, C. N. Moorefield, G. R. Baker, R. K. Behera, G. H. Escamillia and M. J. Saunders, Angew. Chem., Int. Ed. Engl., 1992, 31, 917; J. M. J. Fréchet and I. Gitsov, Macromol. Symp., 1995, 98, 441; V. Percec, P. Chu, G. Ungar and J. Zhou, J. Am. Chem. Soc., 1995, 117, 11441; J. C. M. van Hest, D. A. P. Delnoye, M. W. P. L. Baars, C. Elissen-Román, M. H. P. van Genderen and E. W. Meijer, Chem. Eur. J., 1996, 2, 1616; S. C. Zimmerman, F. Zeng, D. E. C. Reichert and S. V. Kolotuchin, Science, 1996, 271, 1095.
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Fréchet, J.M.J.1
Gitsov, I.2
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Until now, dendrimer-dendrimer interactions involved mainly micelle formation, aggregation or self-assembly in solution, and liquid-crystalline phase transition in the absence of solvent: G. R. Newkome, C. N. Moorefield, G. R. Baker, R. K. Behera, G. H. Escamillia and M. J. Saunders, Angew. Chem., Int. Ed. Engl., 1992, 31, 917; J. M. J. Fréchet and I. Gitsov, Macromol. Symp., 1995, 98, 441; V. Percec, P. Chu, G. Ungar and J. Zhou, J. Am. Chem. Soc., 1995, 117, 11441; J. C. M. van Hest, D. A. P. Delnoye, M. W. P. L. Baars, C. Elissen-Román, M. H. P. van Genderen and E. W. Meijer, Chem. Eur. J., 1996, 2, 1616; S. C. Zimmerman, F. Zeng, D. E. C. Reichert and S. V. Kolotuchin, Science, 1996, 271, 1095.
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Percec, V.1
Chu, P.2
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Until now, dendrimer-dendrimer interactions involved mainly micelle formation, aggregation or self-assembly in solution, and liquid-crystalline phase transition in the absence of solvent: G. R. Newkome, C. N. Moorefield, G. R. Baker, R. K. Behera, G. H. Escamillia and M. J. Saunders, Angew. Chem., Int. Ed. Engl., 1992, 31, 917; J. M. J. Fréchet and I. Gitsov, Macromol. Symp., 1995, 98, 441; V. Percec, P. Chu, G. Ungar and J. Zhou, J. Am. Chem. Soc., 1995, 117, 11441; J. C. M. van Hest, D. A. P. Delnoye, M. W. P. L. Baars, C. Elissen-Román, M. H. P. van Genderen and E. W. Meijer, Chem. Eur. J., 1996, 2, 1616; S. C. Zimmerman, F. Zeng, D. E. C. Reichert and S. V. Kolotuchin, Science, 1996, 271, 1095.
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Van Hest, J.C.M.1
Delnoye, D.A.P.2
Baars, M.W.P.L.3
Elissen-Román, C.4
Van Genderen, M.H.P.5
Meijer, E.W.6
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20
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0030598465
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Until now, dendrimer-dendrimer interactions involved mainly micelle formation, aggregation or self-assembly in solution, and liquid-crystalline phase transition in the absence of solvent: G. R. Newkome, C. N. Moorefield, G. R. Baker, R. K. Behera, G. H. Escamillia and M. J. Saunders, Angew. Chem., Int. Ed. Engl., 1992, 31, 917; J. M. J. Fréchet and I. Gitsov, Macromol. Symp., 1995, 98, 441; V. Percec, P. Chu, G. Ungar and J. Zhou, J. Am. Chem. Soc., 1995, 117, 11441; J. C. M. van Hest, D. A. P. Delnoye, M. W. P. L. Baars, C. Elissen-Román, M. H. P. van Genderen and E. W. Meijer, Chem. Eur. J., 1996, 2, 1616; S. C. Zimmerman, F. Zeng, D. E. C. Reichert and S. V. Kolotuchin, Science, 1996, 271, 1095.
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Kolotuchin, S.V.4
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For hydrogen-bonding in aramides and attractive π-interactions between electron-poor aromatic compounds, see A. P. Bisson and C. A. Hunter, Chem. Commun., 1996, 1723; C. A. Hunter and J. K. M. Sanders, J. Am. Chem. Soc., 1990, 112, 5525.
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For hydrogen-bonding in aramides and attractive π-interactions between electron-poor aromatic compounds, see A. P. Bisson and C. A. Hunter, Chem. Commun., 1996, 1723; C. A. Hunter and J. K. M. Sanders, J. Am. Chem. Soc., 1990, 112, 5525.
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