New N-arylidene (S)-1-phenylethylamines as the components of induced short-pitch cholesterics

Article abstract of DOI:10.1080/10587250108028243

New N-arylidene (S)-1-phenylethylamines with ester group in arylidene fragment have been synthesized. The chiral dopants helical twisting power and temperature dependence of the induced cholesteric helical pitch in LC systems based on 4-pentyl-4′-cyanobip

Full text of DOI:10.1080/10587250108028243

This article was downloaded by: [Gebze Yuksek Teknoloji Enstitïsu ]
On: 20 December 2014, At: 02:12
Publisher: Taylor & Francis
Informa Ltd Registered in England and Wales Registered Number:
1072954 Registered office: Mortimer House, 37-41 Mortimer Street,
London W1T 3JH, UK
Molecular Crystals and
Liquid Crystals Science
and Technology. Section A.
Molecular Crystals and Liquid
Crystals
Publication details, including instructions for
authors and subscription information:
http://www.tandfonline.com/loi/gmcl19
New N-Arylidene (S)-1-
Phenylethylamines as the
Components of Induced
Short-Pitch Cholesterics
L. A. Kutulya a , G. P. Semenkova a , N. I.
Shkolnikova a , V. V. Vashchenko a , L. L. Ostis a ,
V. M. Sorokin b & A. G. Kozachenko b
a Institute for Single Crystals , 60 Lenin Ave,
Kharkov, 61001, Ukraine
b Institute of Semiconductor Physics , 45 Nauki
pr., 03650, Kyiv, Ukraine
Published online: 24 Sep 2006.
To cite this article: L. A. Kutulya , G. P. Semenkova , N. I. Shkolnikova ,
V. V. Vashchenko , L. L. Ostis , V. M. Sorokin & A. G. Kozachenko (2001)
New N-Arylidene (S)-1-Phenylethylamines as the Components of Induced
Short-Pitch Cholesterics, Molecular Crystals and Liquid Crystals Science and
Technology. Section A. Molecular Crystals and Liquid Crystals, 357:1, 43-54, DOI:
10.1080/10587250108028243
To link to this article: http://dx.doi.org/10.1080/10587250108028243
PLEASE SCROLL DOWN FOR ARTICLE

Taylor & Francis makes every effort to ensure the accuracy of all
the information (the “Content”) contained in the publications on our
platform. However, Taylor & Francis, our agents, and our licensors
make no representations or warranties whatsoever as to the accuracy,
completeness, or suitability for any purpose of the Content. Any opinions
and views expressed in this publication are the opinions and views of
the authors, and are not the views of or endorsed by Taylor & Francis.
The accuracy of the Content should not be relied upon and should be
independently verified with primary sources of information. Taylor and
Francis shall not be liable for any losses, actions, claims, proceedings,
demands, costs, expenses, damages, and other liabilities whatsoever
or howsoever caused arising directly or indirectly in connection with, in
relation to or arising out of the use of the Content.
This article may be used for research, teaching, and private study
purposes. Any substantial or systematic reproduction, redistribution,
reselling, loan, sub-licensing, systematic supply, or distribution in any
form to anyone is expressly forbidden. Terms & Conditions of access
and use can be found at http://www.tandfonline.com/page/terms-and-
conditions