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Photopolymerization of Reactive Mesogens

✍ Scribed by Heiko Thiem; Peter Strohriegl; Maxim Shkunov; Iain McCulloch


Book ID
102487033
Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
215 KB
Volume
206
Category
Article
ISSN
1022-1352

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✦ Synopsis


Abstract

Summary: The photopolymerization of two reactive mesogens with photopolymerizable acrylate endgroups, the methyl substituted 1,4‐phenylene‐bis{4‐[6‐(acryloyloxy)hexyloxy]benzoate} 1 and acrylic acid 6‐{4‐[6‐(6‐acryloyloxyhexyloxy)naphthalen‐2‐yl]‐phenoxy}hexyl ester 2 has been investigated using Photo‐DSC measurements. Photocrosslinking of 1 in the nematic phase at 100 °C leads to a final conversion of 87% of the acrylate groups. It is possible to perform photopolymerization with very small amounts of photoinitiator. Even with 0.001% (10 ppm) of photoinitiator, 47% of the acrylate groups polymerize within 15 min. The polymerization of the reactive mesogen 2 proceeds faster in the smectic A phase at 100 °C compared to the isotropic phase at 120 °C and leads to a higher conversion of 75%. This can be explained by an increased local concentration of the acrylate groups between the layers of the smectic cores.

Photopolymerization of reactive mesogens.

magnified imagePhotopolymerization of reactive mesogens.


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## Abstract **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 **