The first examples of discotic liquid crystalline gemini surfactants

Tetrahedron Letters

Volumn 51, Issue 41, 2010, Pages 5459-5462

  Kumar, Sandeep ^a   Gupta, Satyam Kumar ^a  

^a RAMAN RESEARCH INSTITUTE   (India)

Author keywords

Columnar mesophase; Discotic; Gemini surfactant; Imidazole; Ionic liquid crystal; Triphenylene

Indexed keywords

ALKENE DERIVATIVE; GEMINI SURFACTANT; IMIDAZOLE; IONIC LIQUID; SURFACTANT; TRIPHENYLENE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; DIFFERENTIAL SCANNING CALORIMETRY; DIMERIZATION; ENTHALPY; INFRARED SPECTROSCOPY; ION CONDUCTANCE; POLARIZATION MICROSCOPY; PROTON NUCLEAR MAGNETIC RESONANCE; TEMPERATURE SENSITIVITY; ULTRAVIOLET SPECTROSCOPY; X RAY DIFFRACTION;

EID: 81855168059     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.08.022     Document Type: Article

References (51)

1. C.T. Imrie, and P.A. Henderson Chem. Soc. Rev. 36 2007 2096
2. C. Tschierske J. Mater. Chem. 8 1998 1485
3. C.T. Imrie, and G.R. Luckhurst D. Demus, J.W. Goodby, G.W. Gray, H.-W. Spiess, V. Vill, Handbook of Liquid Crystal Vol. 2B 1998 Wiley-VCH Weinheim 801
4. C. Tschierske Curr. Opin. Colloid Interface Sci. 7 2002 355
5. A. Skoulios, and V. Luzzati Acta Crystallogr. 14 1961 278
6. A large number of papers have appeared on thermotropic ionic liquid crystals. It is difficult to cover all these and, therefore, only a few selected references are given here. D.W. Bruce, D.A. Dunmur, E. Lalinde, P.M. Maitlis, and P. Styring Nature 323 1986 791
7. M. Marcos, M.B. Ros, J.L. Serrano, M.A. Esteruelas, E. Sola, L.A. Oro, and J. Barbera Chem. Mater. 2 1990 748
8. E. Bravo-Grim-aldo, D. Navarro-Rodriguez, A. Skoulios, and D. Guillon Liq. Cryst. 20 1996 393
9. H. Bernhardt, W. Weissflog, and H. Kresse Liq. Cryst. 24 1998 895
10. L. Cui, V. Sapagovas, and G. Lattermann Liq. Cryst. 29 2002 1121
11. J. De Roche, C.M. Gordon, C.T. Imrie, M.D. Ingram, A.R. Kennedy, F.L. Celso, and A. Triolo Chem. Mater. 15 2003 3089
12. P.K. Bhowmik, H. Han, I.K. Nedeltchev, and J.J. Cebe Mol. Cryst. Liq. Cryst. 419 2004 27
13. D. Haristoy, and D. Tsiourvas Liq. Cryst. 31 2004 697
14. I.J.B. Lin, and C.S. Vasam J. Organomet. Chem. 690 2005 3498
15. K.M. Lee, C.K. Lee, and I.J.B. Lin Chem. Commun. 1997 899
16. C.M. Gordon, J.D. Holbrey, A.R. Kennedy, and K.R. Seddon J. Mater. Chem. 8 1998 2627
17. J.D. Holbrey, and K.R. Seddon J. Chem. Soc., Dalton Trans. 1999 2133
18. K.M. Lee, Y.T. Lee, and I.J.B. Lin J. Mater. Chem. 13 2003 1079
19. X. Li, D.W. Bruce, and J.M. Shreeve J. Mater. Chem. 19 2009 8232
20. P.H.J. Kouwer, and T.M. Swager J. Am. Chem. Soc. 129 2007 14042
21. M. Yoshio, T. Kato, T. Mukai, M. Yoshizawa, and H. Ohno Mol. Cryst. Liq. Cryst. 413 2004 99
22. M. Yoshio, T. Mukai, H. Ohno, and T. Kato J. Am. Chem. Soc. 126 2004 994
23. M. Yoshio, T. Kagata, K. Hoshino, T. Mukai, H. Ohno, and T. Kato J. Am. Chem. Soc. 128 2006 5570
24. H. Shimura, M. Yoshio, K. Hoshino, T. Mukai, H. Ohno, and T. Kato J. Am. Chem. Soc. 130 2008 1759
25. S. Kumar, and S.K. Pal Tetrahedron Lett. 46 2005 2607
26. S. Kumar, and S.K. Pal Tetrahedron Lett. 46 2005 4127
27. S.K. Pal, and S. Kumar Tetrahedron Lett. 47 2006 8993
28. S.K. Pal, and S. Kumar Liq. Cryst. 35 2008 381
29. K.A. Suresh, and A. Nayak Mol. Cryst. Liq. Cryst. 512 2009 57 [1903]
30. M. Veber, P. Sotta, P. Davidson, A.M. Levelut, C. Jallabert, and H. Strzelecka J. Phys. France 51 1990 1283
31. M. Veber, and G. Berruyer Liq. Cryst. 27 2000 671
32. V. Percec, G. Johansson, J. Heck, G. Ungar, and S.V. Batty J. Chem. Soc., Perkin Trans. 1 1993 1411
33. U. Beginn, G. Zipp, and M. Moller Adv. Mater. 12 2000 510
34. F. Artzner, M. Veber, M. Clerc, and A.M. Levelut Liq. Cryst. 23 1997 27
35. C.F. Van Nostrum, and R.J.M. Nolte Chem. Commun. 1996 2385
36. J. Kadam, C.F.J. Faul, and U. Scherf Chem. Mater. 16 2004 3867
37. F.M. Menger, and C.A. Littau J. Am. Chem. Soc. 113 1991 1451
38. F.M. Menger, and J.S. Keiper Angew chem., Int. Ed. 39 2000 1906
39. Y. Liu, L. Yu, S. Zhang, J. Yuan, L. Shi, and L. Zheng Colloids Surf., A 359 2010 1 3 66
40. S. Fuller, J. Hopwood, A. Rahman, N. Shinde, G.J. Tiddy, G.S. Attard, O. Howell, and S. Sproston Liq. Cryst. 12 1992 521
41. B.A. Pindzola, J. Jin, and D.L. Gin J. Am. Chem. Soc. 125 2003 2940
42. M. Dreja, S. Gramberg, and B. Tieke Chem. Commun. 1998 1371
43. S. Fuller, N.N. Shinde, G.J.T. Tiddy, G.S. Attard, and O. Howell Langmuir 12 1996 1117
44. M. Sikiric, I. Smit, L.T. Bozic, V. Tomasic, I. Pucic, I. Primozic, and N.F. Vincekovic Langmuir 19 2003 10044
45. V. Sharma, M. Borse, S. Devi, K. Dave, J. Pohnerkar, and A. Prajapati J. Dispersion Sci. Technol. 26 2005 421
46. S.J. Ryhänen, A.L. Pakkanen, M.J. Säily, C. Bello, G. Mancini, and P.K.J. Kinnunen J. Phys. Chem. B 106 2002 11694
47. J. Jiang, Z. Shen, J. Lu, P. Fu, Y. Lin, H. Tang, H. Gu, J. Sun, P. Xie, and R. Zhang Adv. Mater. 16 2004 1534
48. S.K. Gupta, V.A. Raghunathan, and S. Kumar New J. Chem. 33 2009 112
49. S.K. Gupta, V.A. Raghunathan, V. Lakshminarayanan, and S. Kumar J. Phys. Chem. B 113 2009 12887
50. 3): δ 7.46 (s, 2H), 7.04 (s, 2H), 6.90 (br s, 2H), 3.91 (m, 4H), 1.75 (m, 4H), 1.1-1.5 (m, 8H).
51. 2O: C, 69.88; H, 9.63; N, 2.43. Found: C, 70.29; H, 9.65; N, 2.26.