A columnar mesophase from a disc-shaped molecule derived from triphenylamine: synthesis, mesomorphic behaviour and optical properties

Tetrahedron Letters

Volumn 48, Issue 36, 2007, Pages 6330-6333

  Majumdar, K C ^a   Pal, Nilasish ^a   Debnath, Pradip ^a   Rao, Nandiraju V S ^b  

^a UNIVERSITY OF KALYANI   (India)

^b ASSAM UNIVERSITY   (India)

Author keywords

Discotic liquid crystal; Hexagonal columnar mesophase; Intermolecular excimer; Triphenylamine derivative

Indexed keywords

ANILINE DERIVATIVE; BENZENE; HYDROXYL GROUP; SCHIFF BASE; TRIPHENYLAMINE; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CHEMICAL STRUCTURE; CYCLIC POTENTIOMETRY; DIFFERENTIAL SCANNING CALORIMETRY; FLUORESCENCE; LIQUID CRYSTAL; PHASE TRANSITION; POLARIZATION MICROSCOPY; SOLVENT EFFECT; SYNTHESIS; X RAY DIFFRACTION;

EID: 34547691655     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.07.026     Document Type: Article

References (19)

1. Boden N., and Movaghar B. In: Demus D., Goodby J., Gray G.W., Spiess H.-W., and Vill V. (Eds). Handbook of Liquid Crystals Vol. 2 (1998), Wiley-VCH, Weinheim 693
2. Chandrasekhar S. In: Demus D., Goodby J., Gray G.W., Spiess H.-W., and Vill V. (Eds). Handbook of Liquid Crystals Vol. 2 (1998), Weinheim, Wiley-VCH 749
3. Kumar S. Chem. Soc. Rev. 35 (2006) 83-109
4. Bushby R.J., and Lozman O.R. Curr. Opin. Colloid Interface Sci. 4 (2002) 343-354
5. Tschierske C. J. Mater. Chem. 11 (2001) 2647-2671
6. Craats A.M., Warman J.M., Mullen K., Geerts Y., and Brand J. Adv. Mater. 10 (1998) 36-38
7. Schouten P.G., Warman J.M., deHaas M.P., Fox M.A., and Pan H.L. Nature 353 (1991) 736-737
8. Vaughan G.B.M., Heiney P.A., McCauley Jr. J.P., and Smith III A.B. Phys. Rev. B 46 (1992) 2787-2791
9. Van de Craats A.M., and Warman J.M. Adv. Mater. 13 (2001) 130-133 and references cited therein
10. Markovitsi D., Marguet S., Bondkowski J., and Kumar S. J. Phys. Chem. B 105 (2001) 1299-1306 and references cited therein
11. Shi W., Fan S., Haung F., Yang W., Liu R., and Cao Y. J. Mater. Chem. 16 (2006) 2387-2394
12. Jiang K.J., Sung Y.L., Shao K.F., and Yang L.M. Chem. Lett. 33 (2004) 50-51
13. Meng F.S., Yao Q.H., Shen J.G., Li F.L., Huang C.H., Chen K.C., and Tian H. Synth. Met. 137 (2003) 1543-1544
14. Cravino A., Roquet S., Leriche P., Aleveque O., Fierre P., and Roncali J. Chem. Commun. (2006) 1416-1418
15. While preparing this Letter the following report was published:. Wang Y.J., Sheu H.S., and Lai C.K. Tetrahedron 63 (2007) 1695-1705
16. Mallegol T., Gmouh S., Meziane M.A.A., Blanchard-Desce M., and Mongin O. Synthesis (2005) 1771-1774
17. Lai G., Bu X.R., Santos J., and Mintz E.A. Synlett (1997) 1275-1276
18. 6, 100 MHz): 165.33, 159.04, 153.82, 150.40, 149.88, 149.56, 143.91, 132.55, 130.58, 128.66, 124.67, 124.60, 123.04, 122.33, 109.13, 73.61, 69.18, 32.36, 31.03, 30.28, 30.25, 30.20, 30.16, 30.12, 29.86, 29.76, 26.67, 26.49, 23.14, 14.39. MALDI-TOF/mass spectra: 2572.91.
19. Camerel F., Bonardi L., Schmutz M., and Ziessel R. J. Am. Chem. Soc. 128 (2006) 4548-4589