A 2-oxazoline monomer bearing a norbornenyl functionality in the side-chain was prepared from the reaction of 5-norbornene-2-carbonitrile and 2-ethanol amine.This monomer could be successfully polymerized using a 2-oxazolinium-based macroinitiator that was in-situ generated from the methyl cation-initiated oligomerization of 2-ethyl- 2-oxazoline. This polymer could be subjected to polymeranalogous reactions involving the alkene groups of the norbornenyl side-chains:A proof-of-concept was established by utilizing the polymers in photoresists that were crosslinked by thiol-ene reactions involving bisfunctional thiols. Photoinitiators for the UV-induced thiol-ene reaction were required in catalytic amounts only. After development, the resists exhibited reproduction of the geometric patterns with a resolution of 30 μm.
CITATION STYLE
Fimberger, M., Schenk, V., Rossegger, E., & Wiesbrock, F. (2014). UV-induced crosslinking of poly [2-(2’-norbornenyl)-2 oxazoline]s. Periodica Polytechnica Chemical Engineering, 58(1), 69–74. https://doi.org/10.3311/PPch.7206
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