Growth of anisotropic single crystals of a random copolymer, poly[(R)-3-hydroxybutyrate-co-(R)-3-hydroxyhexanoate] driven by cooperative -CH center dot center dot center dot O H-bonding

Single crystals of a random copolymer, Poly[(R)-3-hydroxybutyrate-co-(R)-3-hydroxyhexanoate] (PHBHx), with a relatively high (R)-3-hydroxyhexanoate (3HHx) content of 3.9 mol% were grown from dilute solutions over a wide range of crystallization temperatures (T-c) from -20 degrees C to 75 degrees C. Unlike Poly[(R)-3-hydroxybutyrate-co-(R)-3- hydroxyvalerate] (PHBV) which allows the 3-hydroxyvalerate (3HV) to be included into PHB lattice, 3HHx is excluded from the lattice as a non-crystallizable molecular defect. Remarkably, however, even at such a high defect content, all the samples (except for T-c = -20 degrees C) formed well-developed needle-shaped single crystals, with a crystal morphology similar to that found for crystals of the homopolymer PHB. A very characteristic anisotropic lateral growth habit is observed, with the growth rate along the a axis being much higher than that along the b axis. This anisotropic growth pattern was significantly enhanced at T-c = 20 degrees C, wherein the unit cell packing velocity along the a direction is approximately 55 times faster than that along the b direction. This thermal dependent anisotropy was attributed to an unusual cooperative hydrogen bond-like network formed by methyl hydrogen and a neighboring carbonyl oxygen in the alpha crystal of PHB. Another manifestation of this H-bonding network can be seen in unusually thin crystal lamellae at -20 degrees C, with only similar to 6 repeat units per stem, suggesting a superior stability of crystal structure. Interestingly, at this temperature, although 3HHx still cannot be accommodated along the a direction (the H-bonding direction), it could be included along the b direction, indicated by the observation of lattice expansion along the b direction. Also at T-c = -20 degrees C, we found that 3HHx began to show some impact on the crystalline morphology, indicated by the development of a twisted lamellar texture. This effect was believed to arise from the release of stress induced by a congested fold surface dominated by non-crystalline 3HHx and 3HB units.