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Original Articles

Main-Chain Ferroelectric Liquid Crystal Polymers for Electronic Nonlinear Optics Applications Citation1

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Pages 77-82 | Received 01 May 2004, Published online: 07 Sep 2010

REFERENCES

  • Walba , D. M. , Körblova , E. , Shao , R. and Clark , N. A. 2001 . J. Mater. Chem. , 11 : 2743 – 2747 . And references therein
  • alba , D. M. W , Dyer , D. J. , Sierra , T. , Cobben , P. L. , Shao , R. and Clark , N. A. 1996 . J. Am. Chem. Soc. , 118 : 1211 – 1212 . b) D. M.Walba, D. J. Dyer, P. L. Cobben, T. Sierra, J. A. Rego, C. A. Liberko, R. Shao, and N. A. Clark, “Ferroelectric Liquid Crystals for Nonlinear Optics Applications: Can we Really Do It?,” in Thin Films for Integrated Optics Applications, B. W. Wessels, S. R. Marder, and D. M.Walba, Editors, Mat. Res. Soc. Symp. Proc. 392, 157–162 (1995). c) D. M.Walba, D. J. Dyer, X. H. Chen, U. M¨uller, P. Cobben, R. Shao, and N. A. Clark, Mol. Cryst. Liq. Cryst. 288, 83–91 (1996
  • Walba , D. M. , Keller , P. , Shao , R. , Clark , N. A. , Hillmyer , M. and Grubbs , R. H. 1996 . J. Am. Chem. Soc. , 118 : 2740 – 2741 .
  • Keller , P. , Shao , R. , Walba , D. M. , Brunet , M. , Chien , L.-C. , Petschek , R. G. , Bai , F. , Sierra , T. , Omenat , A. , Barberá , J. and Serrano , J. L. 1996 . Liq. Cryst. Polym. Mater. Sci. Eng. Adv. Mater. , 8 : 752 – 756 . c)
  • Walba , D. M. , Xiao , L. , Keller , P. , Shao , R. , Link , D. and Clark , N. A. 1999 . Pure Appl. Chem. , 51 : 2117 – 2123 .
  • All new compounds in the route leading to diene 6 and the polymer showed consistent 1H and 13C NMR spectra. Mesogen 6 and most intermediates gave satisfactory combustion analyses. The structural assignments are quite secure
  • Assignment of the dimer structure, as a mixture of constitutional isomers, was made based upon 1H and 13C NMR spectrometry. End-group analysis by 1H NMR was nicely indicative of dimer
  • In measuring the mesogen length of monomer 6 , a fully extended conformation was generated as an MM2 minimum. The mesogen length l was taken to be the distance between terminal olefinic hydrogen atoms plus twice the covalent radius of hydrogen; l = 37.9 Å. The maximum value of the layer spacing d observed for diene 6 was d = 28.69 Å. The “X-ray tilt” in the smectic C* phase, defined as arccos (d/l) = 40.8°. The “mesogen length” in the polymer was taken as the distance between the mid-points of the terminal double bonds in the fully extended conformation; l = 34.6 Å. The observed layer spacing d = 26.98 Å for the polymer gives a calculated tilt of 38.8° for the polymer smectic C* phase. The mesogen length in the dimer was taken as the distance between either of the above mentioned mid-points and the opposite terminal olefinic hydrogen atom plus one covalent hydrogen radius; l = 36.2 Å. The observed layer spacing of d = 27.67 Å for the dimer gives a calculated tilt of 40.1 Å for the dimer. Due to the low throughput and contrast obtained in SSFLC cells prepared using these materials, reliable optical tilt angles could not be obtained
  • Srinivasarao , M. , Garay , R. O. , Winter , H. H. and Stein , R. S. 1992 . Mol. Cryst. Liq. Cryst. Sci. Technol. Sect. A , 223 : 29 – 39 .

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