Side chain liquid crystalline polyurethanes are a new class of materials th
at show promise for mechanooptic applications. The rich morphology afforded
by these materials also provides a chance to understand the interplay betw
een polyurethane morphology and liquid crystalline ordering. In this paper,
we study the response of a polyurethane with liquid crystals pendant to th
e soft segments to an applied strain using fourier transform infrared (FT-I
R) linear dichroism. We find that this complex material follows the trend e
stablished in the literature for both side chain liquid crystalline homopol
ymers and segmented polyurethanes. At low strains, the soft segments align
with strain inducing an orientation in "lone" hard segments. Up to strains
of 40%, the LC mesogens align with the strain field and the hard segments i
n hydrogen bonded domains align perpendicular to the field. At strains abov
e 40%, we find a rearrangement of the ordering that result in smectic layer
s and the hard segments aligning parallel to the field. A model is proposed
to represent these findings, and reflections on the cooperative movement o
f the different macromolecular components of the polyurethane are offered.
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