We characterize shear-induced states of order and disorder in a symmetric l
amellae forming poly(cyclohexylethylene) (C)-polyethylene (E) CECEC pentabl
ock copolymer. When subjected to a large amplitude reciprocating shear stra
in (gamma = +/-600) in the ordered lamellae state, the sample rapidly align
s in a perpendicular orientation with long-range order. The order-disorder
transition temperature T-ODT-(gamma )decreases with increasing shear rate g
amma, such that a shear rate of gamma = 7 +/- 1 s(-1) is sufficient to diso
rder the material nearly 30 degreesC below the quiescent T-ODT Small-angle
neutron scattering (SANS) from the sheared disordered state displays a symm
etry that suggests a fundamentally different influence of shear compared to
earlier observations of shear-induced anisotropy in the disordered states
of lamellae forming diblock and triblock copolymers. Abrupt cessation of sh
ear leads to spontaneous lamellar ordering into a macroscopically well-alig
ned transverse orientation-an arrangement that previously has been inaccess
ible via processing. In contrast to this behavior, the perpendicular alignm
ent forms when cooling the sample from above the T-ODT while applying low s
hear rates, similar to the response of di- and triblock copolymers. These f
indings shed fresh insight into the complex phenomena that govern flow- and
deformation-induced alignment of block copolymer melts.