Biaxial nematic order and phase behavior studies in an organosiloxane tetrapode using complementary deuterium NMR experiments

C. Cruz, J. L. Figueirinhas, D. Filip, G. Feio, A. C. Ribeiro, Y. Frère, T. Meyer, and G. H. Mehl
Phys. Rev. E 78, 051702 – Published 12 November 2008

Abstract

The biaxial nematic phase was recently observed in different thermotropic liquid crystals, namely bent-core compounds, side-chain polymers, bent-core dimers, and organosiloxane tetrapodes. In this work, a series of experiments with a nematic organosiloxane tetrapode where nuclear magnetic resonance (NMR) spectra are collected while the sample is continuously rotating around an axis perpendicular to the magnetic field, are discussed in conjunction with the analysis of a deuterium NMR experiment on the same system reported earlier. The sample used is a mixture of a deuterated probe with the tetrapode. The mixture exhibits a nematic range between 40°C and 37°C. The results of the two independent, but complementary deuterium NMR experiments confirm the existence of a biaxial nematic phase for temperatures below 0°C with high values of the asymmetry parameter at low temperatures. The presence of slow movements of the tetrapode mesogenic units in the low-temperature regime could also be detected through the analysis of the NMR spectra. Simulations indicate that these movements are mainly slow molecular reorientations of the mesogenic units associated with the presence of collective modes in the nematic phases of this compound. In the case of tetrapodes, recent investigations attribute the origin of biaxiality to the hindering of reorientations of the laterally attached mesogenic units which constitute the tetrapode. This study relates the molecular movements with the nematic biaxial ordering of the system.

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  • Received 10 May 2006

DOI:https://doi.org/10.1103/PhysRevE.78.051702

©2008 American Physical Society

Authors & Affiliations

C. Cruz1,2, J. L. Figueirinhas1,2, D. Filip1,3, G. Feio1,4, A. C. Ribeiro1,2, Y. Frère5, T. Meyer6, and G. H. Mehl6

  • 1CFMC-UL, Av. Prof. Gama Pinto 2, 1649-003 Lisboa, Portugal
  • 2IST, Av. Rovisco Pais, 1049-001 Lisboa, Portugal
  • 3“Petru Poni” Institute of Macromolecular Chemistry, Aleea Gr. Ghica Voda 41 A, 700487-Iasi, Romania
  • 4CENIMAT, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, 2829-516 Caparica, Portugal
  • 5Institut Charles Sadron, UPR22-CNRS, 6, rue Boussingault-BP 40016, F-67083 Strasbourg Cedex, France
  • 6Department of Chemistry, The University of Hull Cottingham Road, Hull, HU6 7RX, United Kingdom

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Issue

Vol. 78, Iss. 5 — November 2008

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