Using a home-built
rheo-NMR apparatus with Couette geometry that
allows pulse program-controlled switching of spinning speeds, the
formation of liquid crystalline phases of poly-γ-benzyl-l-glutamate (PBLG) in CDCl3 is studied at concentrations
up to 15% (w/v) using deuterium NMR of the solvent under static and
shear force conditions. A tilt of director alignment from 0 to ≈75–79°
is observed. While the well-known first-order phase transition from
isotropic to the liquid crystalline phase is detected in the static
case, the transition vanishes under applied shear with freely scalable
partial alignment down to the lowest concentrations measured. Close
to the static phase transition concentration, a coexistence of isotropic
and aligned phases is observed when a cosolute is added, which disappears
upon application of shear forces. Temperature, concentration, and
shear-rate-dependent alignment properties are characterized. In addition,
kinetic studies involving the switching of shear forces reveal buildup
rates for the phases in the range of milliseconds to minutes, which
allowed the acquisition of an unaligned/aligned 2D correlation experiment
in a favorable case. Finally, the usefulness of very low, rheo-induced
alignment for the measurement of residual dipolar couplings is demonstrated.