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Cholesteric liquid crystal glass platinum acetylides

Published online by Cambridge University Press:  21 August 2014

Thomas M. Cooper
Affiliation:
Materials and Manufacturing Directorate, Air Force Research Laboratory, Wright-Patterson Air Force Base, OH, 45433
Aaron R. Burke
Affiliation:
Materials and Manufacturing Directorate, Air Force Research Laboratory, Wright-Patterson Air Force Base, OH, 45433
Douglas M. Krein
Affiliation:
Materials and Manufacturing Directorate, Air Force Research Laboratory, Wright-Patterson Air Force Base, OH, 45433
Ronald F. Ziolo
Affiliation:
Centro de Investigacion en Quimica Aplicada(CIQA), Boulevard Enrique Reyna 140,25294 Saltillo, Coahuila, Mexico
Eduardo Arias
Affiliation:
Centro de Investigacion en Quimica Aplicada(CIQA), Boulevard Enrique Reyna 140,25294 Saltillo, Coahuila, Mexico
Ivana Moggio
Affiliation:
Centro de Investigacion en Quimica Aplicada(CIQA), Boulevard Enrique Reyna 140,25294 Saltillo, Coahuila, Mexico
Albert Fratini
Affiliation:
Department of Chemistry, University of Dayton, Dayton, OH 45469
Yuriy Garbovskiy
Affiliation:
Department of Physics, University of Colorado at Colorado Springs, Colorado Springs, CO 80933
Anatoliy V. Glushchenko
Affiliation:
Department of Physics, University of Colorado at Colorado Springs, Colorado Springs, CO 80933
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Abstract

To prepare cholesteric liquid crystalline nonlinear optical materials with ability to be vitrified on cooling and form long time stability cholesteric glasses at room temperature, a series of platinum acetylide complexes modified with cholesterol has been synthesized. The materials synthesized have the formula trans-Pt(PR3)(cholesterol (3 or 4)-ethynyl benzoate)(1-ethynyl-4-X-benzene), where R = Et, Bu or Oct and X = H, F, OCH3 and CN. A cholesteric liquid crystal phase was observed in the complexes R = Et, and X = F, OCH3 and CN but not in any of the other complexes. When X = CN, a cholesteric glass was observed at room temperature which remained stable up to 130 °C, then converted to a mixed crystalline/cholesteric phase and completely melted to an isotropic phase at 230 °C. When X = F or OCH3 the complexes were crystalline at room temperature with conversion to the cholesteric phase upon heating to 190 and 230 °C, respectively. In the series X = CN, OCH3 and F, the cholesteric pitch was determined to be 1.7, 3.4 and 9.0 µ, respectively.

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Articles
Copyright
Copyright © Materials Research Society 2014 

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References

REFERENCES

(a) Rogers, J.E., Slagle, J.E., Krein, D.M., Burke, A.R., Hall, B.C., Fratini, A., Fleitz, P.A., Cooper, T.M., Drobizhev, M., Makarov, N.S., Rebane, A., Kim, K.-Y., Farley, R. and Schanze, K.S. Inorg. Chem. 46, 6483 (2007); (b)Haley, J.E., Krein, D.M., Monahan, J.L., Burke, A.R., McLean, D.G., Slagle, J.E., Fratini, A. and Cooper, T.M. J. Phys. Chem. A 115, 265 (2011); (c) Rebane, A., Drobizhev, M., Makarov, N.S., Beuerman, E., Haley, J.E., Krein, D.M., Burke, A.R., Flikkema, J.L. and Cooper, T.M. J. Phys. Chem. A 115, 4255 (2011); (d) Cooper, T.M., Krein, D.M., Burke, A.R., McLean, D.G., Haley, J.E., Slagle, J., Monahan, J. and Fratini, A., J. Phys. Chem. A 116, 139 (2012).Google Scholar
Liao, C., Shelton, A.H., Kim, K.-Y. and Schanze, K.S. ACS Appl. Mater. Interfaces, 3, 3225 (2011).CrossRefGoogle Scholar
Slagle, J.E., Cooper, T.M., Krein, D.M., Rogers, J.E., McLean, D.G. and Urbas, A.M. Chem. Phys. Lett., 447, 65 (2007).Google Scholar
(a) Bunning, T.J., Mather, P.T., Barnes, W. and Hood, P.J. Liq. Cryst, 26, 557 (1999); (b) Chen, S.H., Mastrangelo, J.C. and Jin, R. J. Adv. Matl.,11, 1135 (1999).CrossRefGoogle Scholar
Chen, H., Katsis, D., Mastrangelo, J., Chen, S., Jacob, S. and Hood, P.J. Adv. Matls. 12, 1283 (2000).3.0.CO;2-P>CrossRefGoogle Scholar
Kumar, N.S., Abraham, S., Ratheesh, K., Tamaoki, N., Furumi, S. and Das, S. J. Photochem. Photobiol. A: Chemistry 73, 207 (2009).Google Scholar
Tamaoki, N. N. Adv. Matl. 13, 1135 (2001).3.0.CO;2-S>CrossRefGoogle Scholar
Furumi, S., Chem. Rec. 10, 394 (2010).Google Scholar
Dierking, I., ., Textures of Liquid Crystals, (Wiley-VCH Verlag Gmbh & Co., Weinheim, 2003)Google Scholar