Transition temperature engineering of octaalkoxycarbonyl phthalocyanines

Journal of Materials Chemistry

Volumn 17, Issue 29, 2007, Pages 3002-3007

  Sergeyev, Sergey ^a   Debever, Olivier ^a   Pouzet, Eric ^a   Geerts, Yves Henri ^a  

^a UNIVERSITÉ LIBRE DE BRUXELLES   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

BINARY MIXTURES; ESTERIFICATION; SUPERCONDUCTING TRANSITION TEMPERATURE;

ALKYL CHAINS; ISOTROPIZATION; OCTAACID PRECURSORS; THERMOTROPIC PROPERTIES;

ALCOHOLS;

EID: 34547143264     PISSN: 09599428     EISSN: 13645501     Source Type: Journal    
DOI: 10.1039/b704344a     Document Type: Article

References (27)

1. D. Adam P. Schuhmacher J. Simmerer L. Haussling K. Siemensmeyer K. H. Etzbach H. Ringsdorf D. Haarer Nature 1994 371 141 143
2. V. Lemaur D. A. da Silva Filho V. Coropceanu M. Lehmann Y. Geerts J. Piris M. G. Debije A. M. van de Craats K. Senthilkumar L. D. A. Siebbeles J. M. Warman J.-L. Bredas J. Cornil J. Am. Chem. Soc. 2004 126 3271 3279
3. S. Kumar Chem. Soc. Rev. 2006 35 83 109
4. A. N. Cammidge and R. J. Bushby, in Handbook of Liquid Crystals, ed., D. Demus, J. W. Goodby, G. W. Gray, H. W. Spiess, and, V. Vill, Wiley-WCH, Weinheim, 1998, vol. 2B, ch. 7, pp. 693-747
5. M. D. Watson A. Fechtenkötter K. Müllen Chem. Rev. 2001 101 1267 1300
6. R. J. Bushby O. R. Lozman Curr. Opin. Colloid Interface Sci. 2002 7 343 354
7. S. Sergeyev W. Pisula Y. H. Geerts Chem. Soc. Rev. 2007 10.1039/b417320c
8. G. de la Torre C. G. Classens T. Torres Chem. Commun. 2007 2000 2015
9. C. Piechocki J. Simon A. Skoulios D. Guillon P. Weber J. Am. Chem. Soc. 1982 104 5245 5247
10. D. Guillon A. Skoulios C. Piechocki J. Simon P. Weber Mol. Cryst. Liq. Cryst. 1983 100 275 284
11. K. Ohta L. Jacquemin C. Sirlin L. Bosio J. Simon New J. Chem. 1988 12 751 754
12. H. Iino J. Hanna R. J. Bushby B. Movaghar B. J. Whitaker M. J. Cook Appl. Phys. Lett. 2005 87 132102
13. H. Sirringhaus P. J. Brown R. H. Friend M. M. Nielsen K. Bechgaard B. M. W. Langeveld-Voss A. J. H. Spiering R. A. J. Janssen E. W. Meijer P. Herwig D. M. de Leeuw Nature 1999 401 685 688
14. C. D. Simpson J. S. Wu M. D. Watson K. Müllen J. Mater. Chem. 2004 14 494 504
15. V. de Cupere J. Tant P. Viville R. Lazzaroni W. Osikowicz W. R. Salaneck Y. H. Geerts Langmuir 2006 22 7798 7806
16. W. A. MacDonald J. Mater. Chem. 2004 14 4 10
17. B. Schartel A. Kettner R. Kunze J. H. Wendorff M. Hennecke Adv. Mater. Opt. Electron. 1999 9 55 64
18. S. Sergeyev E. Pouzet O. Debever J. Levin J. Gierschner J. Cornil R. Gomez-Aspe Y. H. Geerts J. Mater. Chem. 2007 17 1777 1784
19. For the sake of clarity, we use the following widely accepted notation system: Cn,m refers to the branched 2-(alkyl')alkyl, where n and m are the number of carbon atoms in the alkyl and alkyl' radicals, respectively
20. N. B. McKeown, Phthalocyanine Materials: Synthesis, Structure and Function, University Press, Cambridge, 1998
21. N. B. McKeown M. Helliwell B. M. Hassan D. Hayhurst H. Li N. Thompson S. J. Teat Chem.-Eur. J. 2007 13 228 234
22. A. M. Levelut J. Chem. Phys. 1983 88 149 161
23. S. Saidi-Besbes E. Grelet H. Bock Angew. Chem., Int. Ed. 2006 45 1783 1786
24. T. Hassheider S. A. Benning H.-S. Kitzerow M.-F. Achard H. Bock Angew. Chem., Int. Ed. 2001 40 2060 2063
25. T. Hassheider S. A. Benning M. W. Lauhof H. S. Kitzerow H. Bock M. D. Watson K. Müllen Mol. Cryst. Liq. Cryst. 2004 413 2597 2608
26. A. C. Grimsdale J. Wu K. Müllen Chem. Commun. 2005 2197 2204
27. L. Dulog A. Gittinger Mol. Cryst. Liq. Cryst. 1992 213 31 42