Liquid crystals showing a molecular rearrangement: a dynamic NMR study of a 2-benzoyloxytropone mesogen

Article abstract of DOI:10.1080/10587259608034071

The [1,9] sigmatropic rearrangement has been studied by Dynamic NMR spectroscopy for a 2-benzoyloxytropone mesogen. The proton spectra of the compound in CDCl₃ and C₆D₆ as isotropic solvents have been recorded in the range

Full text of DOI:10.1080/10587259608034071

This article was downloaded by: [University of Glasgow]
On: 02 January 2015, At: 16:53
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
Liquid Crystals Showing a Molecular
Rearrangement: A Dynamic NMR Study of
a 2-Benzoyloxytropone Mesogen
D. Catalano a , M. Cavazza a , E. Ciampi a & C. A. Veracini a
a Dipartimento di Chimica e Chimica industriale , via Risogimento
35, 1-56126, Pisa
Published online: 12 Jun 2011.
To cite this article: D. Catalano , M. Cavazza , E. Ciampi & C. A. Veracini (1996) Liquid Crystals
Showing a Molecular Rearrangement: A Dynamic NMR Study of a 2-Benzoyloxytropone Mesogen,
Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and
Liquid Crystals, 275:1, 163-174, DOI: 10.1080/10587259608034071
To link to this article: http://dx.doi.org/10.1080/10587259608034071
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