INFLUENCE OF THE ANGULAR LINKAGE ON THE MESOMORPHIC PROPERTIES OF CHOLESTERYL ARYLBENZOATES.

Article abstract of DOI:10.1080/00268948208072592

Some cholesteryl esters of arylbenzoic acids incorporating angular linkage such as -Co-, -O-, -S-, and -CH//2-, were prepared, and the transition temperatures and heats determined. The cholesteric-isotropic transition temperatures are likely to correlate with the angular correlation parameters of these carboxylic acid moieties. The mesomorphic phenomena are discussed in terms of the molecular structure and electronic effect of these linkages.

Full text of DOI:10.1080/00268948208072592

This article was downloaded by: [Michigan State University]
On: 08 February 2015, At: 23:06
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
Publication details, including instructions for
authors and subscription information:
http://www.tandfonline.com/loi/gmcl16
Influence of the Angular
Linkage on the Mesomorphic
Properties of Cholesteryl
Arylbenzoates
M. Koden a , S. Takenaka a & S. Kusabayashi a
a Department of Applied Chemistry , Faculty of
Engineering, Osaka University , Suita, Osaka, 565,
Japan
Published online: 13 Dec 2006.
To cite this article: M. Koden , S. Takenaka & S. Kusabayashi (1982) Influence
of the Angular Linkage on the Mesomorphic Properties of Cholesteryl
Arylbenzoates, Molecular Crystals and Liquid Crystals, 88:1-4, 137-150, DOI:
10.1080/00268948208072592
To link to this article: http://dx.doi.org/10.1080/00268948208072592
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