Synthesis and Orientation of Fluorene Containing Reactive Mesogens

The synthesis of new fluorene containing photocrosslinkable reactive mesogens is described. Both monodisperse trimers or pentamers and oligomeric mixtures containing two photocrosslinkable acrylate end groups were obtained by Suzuki‐cross‐coupling reactions. The pentamer 12a shows an ideal phase beh...

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Bibliographic Details
Published in:Macromolecular chemistry and physics Vol. 207; no. 4; pp. 370 - 381
Main Authors: Thiem, Heiko, Jandke, Markus, Hanft, Doris, Strohriegl, Peter
Format: Journal Article
Language:English
Published: Weinheim WILEY-VCH Verlag 24-02-2006
WILEY‐VCH Verlag
Wiley
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Summary:The synthesis of new fluorene containing photocrosslinkable reactive mesogens is described. Both monodisperse trimers or pentamers and oligomeric mixtures containing two photocrosslinkable acrylate end groups were obtained by Suzuki‐cross‐coupling reactions. The pentamer 12a shows an ideal phase behavior for orientation experiments with a broad nematic phase between the glass transition at −10 °C and 123 °C. In the oligomeric mixtures 14a–g the transition temperature from the nematic to the isotropic phase can be tailored from 100 to 310 °C by adjusting the molecular weight of the oligomers by end‐capping. This process can be easily characterized by MALDI‐TOF spectroscopy. The pentamer 12a and the oligomeric mixture 14c were oriented on rubbed polyimide layers and orientation ratios of 15:1 in photoluminescence were obtained. Experiments with different film thicknesses show that the orientation is not homogeneous throughout the film but decreases with increasing distance from the orientation layer.
Bibliography:istex:0A56480F9968E9C4F3B3C4E658C2C8CEAF1483B8
ark:/67375/WNG-KDWMHV3S-2
ArticleID:MACP200500455
ISSN:1022-1352
1521-3935
DOI:10.1002/macp.200500455