48
Views
10
CrossRef citations to date
0
Altmetric
Original Articles

Deuterium NMR Investigation of the Influence of Molecular Structure on the Biaxial Ordering of Organosiloxane Tetrapodes Nematic Phase

, , , , , , & show all
Pages 348/[700]-359/[711] | Published online: 30 Jan 2009
 

Abstract

In order to contribute to the understanding of the origin of biaxial nematic ordering in tetrapodes, a deuterium NMR study was performed on mixtures of monomers from organosiloxane tetrapodes with a deuterated nematic probe. Contrary to the tetrapode system previously studied, which exhibits a biaxial nematic phase, the results for monomers are compatible, within the experimental error, with uniaxial nematic ordering in the whole nematic range. The data are in agreement with the conjecture that the nematic biaxial behaviour is related to hindering of the mesogenic units' rotational movements, arising from interdigitation and connection to the central silicon core.

Acknowledgments

The authors thank Dr. Yves Frère (ICS, Strasbourg, France) for the synthesis of the deuterated probe.

M. Cardoso thanks Calouste Gulbenkian Foundation and Instituto Superior Técnico for Professor António da Silveira grant.

This work was partially supported by the Portuguese Science and Technology Foundation (FCT) projects: POCTI/ISFL/261-516 and PTDC/FIS/65037/2006.

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.