Paper
RSC Advances
Additionally, we have demonstrated an improved method of the 20 Z. Raszewski, E. Kruszelnicki-Nowinowski, J. K˛edzierski,
bistolane core synthesis. Here we used the presence of the steric
hindrance generated by the lateral alkyl group. This allowed us
P. Perkowski, W. Piecek, R. D˛abrowski, P. Morawiak and
K. Ogrodnik, Mol. Cryst. Liq. Cryst., 2010, 525, 125–140.
to gain the regioselectivity of the Sonogashira cross-coupling 21 C. L. Pan and R. P. Pan, Liq. Cryst. Mater. Devices Appl. XI,
reaction in the crucial stage of the bistolane synthesis.
2006, 6135, 61350D1.
´
22 V. Urruchi, C. Marcos, J. Torrecilla, J. M. Sanchez-Pena and
K. Garbat, Rev. Sci. Instrum., 2013, 84, 026102.
Acknowledgements
23 A. M. Urbas and D. P. Brown, Liquid crystals in
metamaterials, in Liquid Crystals Beyond Displays:
Chemistry, Physics, and Applications, ed. O. Li, John
Wiley&Sons, Inc., Hoboken, NJ, USA, 2012, pp. 379–402.
24 I. C. Khoo, D. H. Werner, X. Liang, A. Diaz and B. Weiner,
Opt. Lett., 2006, 31, 2592–2594.
This work was carried out with nancial support from the
Polish Ministry of Science and Higher Education, Key Project
POIG.01.03.01-016/08 “New photonic materials and their
advanced application”.
25 R. Pratibha, K. Park, I. Smalyukh and W. Park, Opt. Express,
2009, 17, 19459–19469.
References
1 R. D˛abrowski, P. Kula and J. Herman, Crystals, 2013, 3(3), 26 O. D. Lavrentovich, Proc. Natl. Acad. Sci. U. S. A., 2011, 108,
443–482. 5143–5144.
2 P. Kirsch and M. Bremer, Angew. Chem., Int. Ed., 2000, 39, 27 J. Herman, J. Dziaduszek, R. D˛abrowski, J. K˛edzierski,
4216–4235.
K. Kowiorski, V. S. Dasari, S. Dhara and P. Kula, Liq. Cryst.,
2013, 40(9), 1174–1182.
28 Y. Arakawa, S. Kang, J. Watanabe and G. Konishi, Phase
Transitions, 2015, 88, 1181–1192.
29 C. Viney, D. J. Brown, C. M. Dannels and R. J. Twieg, Liq.
Cryst., 1993, 13, 95–100.
3 Y. Iwashita, M. Kaneoya, K. Takeuchi, S. Takehara and
H. Takatsu, Mol. Cryst. Liq. Cryst., 2001, 364, 851–858.
4 D. Pauluth and K. Tarumi, J. Mater. Chem., 2004, 14, 1219–
1227.
5 P. A. Breddels, Proceedings of the 12th International Topical
Meeting on Optics of Liquid Crystals (OLC'07), Puebla City, 30 Y. Xu, Y. Hu, Q. Chen and J. Wen, J. Mater. Chem., 1995, 5,
Mexico, 1–5 October2007, pp. 17–20.
219–221.
6 C. O. Catanescu, L. C. Chien and S. T. Wu, Mol. Cryst. Liq. 31 R. J. Twieg, V. Chu, C. Nguyen, C. M. Dannels and C. Viney,
Cryst., 2004, 411, 93–102.
Liq. Cryst., 1996, 20, 287–292.
7 P. Kirch, Applications of organouorine compounds, in 32 N. Leroux and L. C. Chien, Liq. Cryst., 1996, 21, 189–195.
Modern Fluoroorganic Chemistry: Synthesis, Reactivity, 33 S. T. Wu, C. S. Hsu and Y. Y. Chuang, Jpn. J. Appl. Phys., 1999,
Applications, Willey-VCH Verlag GmbH: Weinhaim,
Germany, 2004, pp. 213–225.
8 M. Schadt, Liq. Cryst., 1993, 14, 73–104.
38, L286–L288.
34 N. Li, Z. Li, X. Zhang and R. Hua, Int. J. Mol. Sci., 2013, 14,
23257–23273.
9 S. T. Wu, C. S. Hsu, Y. Y. Chuang and H. B. Cheng, Jpn. J. 35 S. T. Wu, C. S. Hsu, Y. Y. Chuang and H. B. Cheng, Jpn. J.
Appl. Phys., 2000, 39, L38–L41.
Appl. Phys., 2000, 39, L38–L41.
10 R. W˛egłowski, S. J. Kłosowicz and A. Majchrowski, Mater. 36 C. S. Hsu, K. F. Shyu, Y. Y. Chuang and S. T. Wu, Liq. Cryst.,
Lett., 2010, 64(10), 1176–1178. 2000, 27(2), 283–287.
11 R. W˛egłowski, S. J. Kłosowicz, A. Majchrowski, K. Ozga, 37 S. T. Wu, C. S. Hsu and K. F. Shyu, Appl. Phys. Lett., 1999,
I. Kityk, S. Calus and M. Chmiel, Optic. Laser. Eng., 2010,
48(9), 856–858.
12 S. T. Wu, J. D. Margerum, H. B. Meng, C. S. Hsu and
L. R. Dalton, Appl. Phys. Lett., 1994, 64, 1204–1206.
13 S. T. Wu, Opt. Eng., 1987, 26, 120–128.
14 X. Y. Nie, T. X. Wu, Y. Q. Lu, Y. H. Wu, X. Liang and S. T. Wu,
Mol. Cryst. Liq. Cryst., 2006, 454, 123–133.
15 N. Vieweg, N. Born, I. Al-Naib and M. Koch, J. Infrared,
Millimeter, Terahertz Waves, 2012, 33, 327–332.
74(3), 344–346.
38 V. Reiffenrath, C. Jasper, A. Manabe, E. Montenegro and
D. Pauluth, United States Patent Application Publication,
Pub. No.: US 2013/0221274 A1, Aug. 29, 2013.
39 D. Demus and H. Zaschke, Flussige Kristalle in Tabellen II,
VEB Deutcher Verlag fur Grundstoffindustrie, Leipzig, 1984.
40 D. Demus, J. W. Goodby, G. W. Gray, H. W. Spiess and V. Vill,
Handbook of liquid crystals. Low molecular weight liquid
crystals I, Wiley-VCH, Weinheim, 1998, vol. 2A, p. 530.
16 C. J. Lin, C. H. Lin, Y. T. Li, R. P. Pan and C. L. Pan, IEEE 41 Atomic and Molecular Polarizabilities, in CRC Handbook of
Photonics Technol. Lett., 2009, 21(11), 730–732.
17 F. Dubois, F. Krasinski, B. Splingart, N. Tentillier,
C. Legrand, A. Spadło and R. D˛abrowski, Jpn. J. Appl. Phys.,
2008, 47, 3564–3567.
Chemistry and Physics, Internet Version 2005, ed. D. R. Lide,
CRC Press, Boca Raton, FL, 2005, http://
42 M. F. Vuks, Opt. Spectrosc., 1966, 20, 644–651.
18 H. Y. Wu, C. F. Hsieh, T. T. Tang, R. P. Pan and C. L. Pan, 43 G. te Velde, F. M. Bickelhaupt, S. J. A. van Gisbergen,
IEEE Photonics Technol. Lett., 2006, 18, 1488–1490.
19 Y. Garbovskiy, V. P. Zagorodnii, J. Lovejoy, R. E. Camley,
C. F. Guerra, E. J. Baerends, J. G. Snijders and T. Ziegler, J.
Comput. Chem., 2001, 22, 931–967.
´
Z. Celinski, A. Glushchenko, J. Dziaduszek and 44 C. Fonseca Guerra, J. G. Snijders, G. te Velde and
R. D˛abrowski, J. Appl. Phys., 2012, 111, 054504.
E. J. Baerends, Theor. Chem. Acc., 1998, 99, 391–403.
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