274
AKOPOVA et al.
11. Perova, T.S. and Vij, J.K., Mol. Cryst. Liq. Cryst., 1995,
log ε: 369/3.77; 351/3.95; 306/4.57; 278/5.24;
213/4.25. IR spectrum (KBr), n, cm–1: 1771 (–С–О,
cyclic ketone), 1700 (–C = C), 1650 (d, NH, anilide),
vol. 263, p. 293.
12. Bock, H. and Helfrich, W., Liq. Cryst., 1995, vol. 18,
1
no. 3, p. 387.
1262 (–C–N, secondary amine), 1250 (–C–C = O). Н
13. Heppke, G., Krüerke, D., Löhning, C., Lötzsch, D.,
Rauch, S., and Sharma, N.K., Abstract of Papers, 26
Freiburger Arbeitstagung Flussigkristalle, Freiburg,
Germany, 1997, P-71.
14. Bagordo, G., Helfrich, W., and Rapp, G., Abstract of
Papers, 27 Freiburger Arbeitstagung Flussigkristalle,
Freiburg, Germany, 1998, P-66.
NMR spectrum, δ, ppm: 3.65 s (2H, CO–CH2), 4.02,
4.04, 4.07 m (3H, CO–CH), 7.05 s (1H, ArH), 7.37 s
(1H, ArH), 7.41 s (1H, ArH), 7.45 s (1H, ArH), 8.52 s
(1H, NH). 13C NMR spectrum, δС, ppm: (s) 14.04,
22.52, 26.14, 31.79, 72.18; (d) 105.94, 107.37, 109.31;
(t) 123.97; (m) 29.16, 29.49, 30.51, 67.78, 68.38,
68.76, 148.08.
15. Isabel, M. and Goodby, W., J. Mater. Chem., 2001,
vol. 11, p. 2845.
ACKNOWLEDGMENTS
16. Pisula, W., Kastler, M., Wasserfallen, D., Pakula, T.,
and Müllen, K., J. Am. Chem. Soc., 2004, vol. 126,
p. 8074.
17. Achen, R., Koudijs, A., Giesbers, M., Reddy, R.A.,
Verhulst, T., Tschierske, C., Marcelis, A.T.M., and
Sudhölter, E.J.R., Liq. Cryst., 2006, vol. 33, no. 6,
p. 681.
This work was supported by the grant
“Development of integration mechanisms of the
ducational and scientific process in the field of
nanomaterials” (project no. RNP 2.2.1.1. 7280).
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