28
Views
24
CrossRef citations to date
0
Altmetric
Original Articles

Multiple contributions to potentials of mean torque for solutes dissolved in liquid crystal solvents. A comparison of the orientational ordering of anthracene and anthraquinone as solutes in nematic solvents

, , , , , , , & show all
Pages 649-660 | Received 19 Oct 1990, Accepted 26 Jan 1991, Published online: 24 Sep 2006
 

Abstract

The two principal orientational order parameters of anthracene and anthraquinone as solutes in several liquid crystal solvents have been obtained via deuterium NMR spectra. The ordering of anthraquinone is much more solvent dependent than that of anthracene, and possible explanations of this behaviour are examined. In particular, the possibility that electrostatic as well as dispersive and repulsion forces could contribute to a mean field potential is explored. It is concluded that the most probable cause of the large differences in orientational ordering of these two molecules in some solvents, but not in others, is a dependence on both solute and solvent of order parameters C + 4,0 and C + 2,0 for the distribution of solute-solvent intermolecular vectors.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.