Effect of chain topology on the self-organization and dynamics of block copolypeptides: from diblock copolymers to stars.

The effect of chain topology on (i) the peptide secondary structure, (ii) the nanophase self-assembly, and (iii) the local segmental and global peptide relaxations has been studied in a series of model diblock and 3-arm star copolypeptides of poly(epsilon-carbobenzyloxy-L-lysine) (PZLL) and poly(gamma-benzyl-L-glutamate) (PBLG) with PZLL forming the core. Diblock copolypeptides are nanophase separated with PBLG and PZLL domains comprising alpha-helices packed in a hexagonal lattice. Star copolypeptides are only weakly phase separated, comprising PBLG and PZLL alpha-helices in a pseudohexagonal lattice. Phase mixing has profound consequences on the local and global dynamics. The relaxation of the peptide secondary structure speeds up, and the helix persistence length is further reduced in the stars, signifying an increased concentration of helical defects.

Self-assembly of pODMA-b-ptBA-b-pODMA triblock copolymers in bulk and on surfaces. A quantitative SAXS/AFM comparison.

The phase state of a series of poly(n-octadecyl methacrylate)-b-poly(tert-butyl acrylate)-b-poly(n-octadecyl methacrylate) (pODMA-b-ptBA-b-pODMA) triblock copolymers, synthesized through atom transfer radical polymerization, has been investigated in bulk and on surfaces using small-angle X-ray scattering and atomic force microscopy, respectively. The mean-field theory was employed to construct the bulk phase diagram. Excellent agreement was found between the bulk and surface morphologies as well as for the domain spacing (domain spacing scaled as d approximately equal to N(0.64)), suggesting that the strong polymer-polymer interactions in bulk are also the dominant interactions on surfaces.

Effects of temperature and pressure on the stability and mobility of phases in rigid rod poly (p-phenylenes).

The structure and the associated dynamics have been investigated in melts of hairy-rod macromolecules composed from a poly(p-phenylene) backbone with sulfonate ester and dodecyl side chains. For the structure investigation, polarizing optical microscopy, differential scanning calorimetry, pressure-volume-temperature, and wide-angle x-ray scattering have been employed whereas for the dynamics dielectric spectroscopy as a function of temperature and pressure was used. Based on the combined information from structure and dynamics the relaxation mechanisms were identified and the origin of the glass transition has been discussed in terms of insufficient thermal energy rather than insufficient free volume. The relevant phase diagram has been constructed and the stability and mobility of phases is discussed.