Self-assembly of crystalline bioinspired block copolymers

ORAL

Abstract

Polypeptoids are sequence-specific biologically inspired polymers based on N-substituted glycines for which monodisperse, polymeric molecular weights can be achieved. Sequence control allows for a degree of tunability in both the self-assembly and thermal properties not available in classical polymer systems. We demonstrate that a series of homopolypeptoids are thermally stable to 300C and are crystalline with melting transitions ranging from 150C to 250C. The introduction of defects at precise locations in the polymer sequence (as a side chain substitution) allows crystallization and hence the melting temperature to be suppressed. Symmetric block copolymers with two crystalline polypeptoid blocks exhibit co-crystallization of the two blocks but distinct melting behaviors, indicating a disordered melt. If samples are carefully prepared to allow for microphase separation, block copolymer lamellae with long range order are formed with an order-disorder transition temperature well below the melting transition temperature of the polymer.

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Authors

  • A.M. Rosales

    Dept. of Chemical Engineering, University of California-Berkeley, Dept. of Chemical Engineering, University of California - Berkeley

  • H.K. Murnen

    Dept. of Chemical Engineering, University of California-Berkeley, Dept. of Chemical Engineering, University of California - Berkeley

  • R.N. Zuckermann

    Molecular Foundry, Lawrence Berkeley National Laboratory

  • R.A. Segalman

    Dept. of Chemical Engineering, University of California-Berkeley, Dept of Chemical Engineering, University of California-Berkeley, UC Berkeley and Lawrence Berkeley National Laboratories, UC Berkeley, Department of Chemical Engineering, University of California, Berkeley, UC Berkeley and Lawrence Berkeley National Laboratory, UC Berkeley Chemical Engineering, Dept. of Chemical Engineering, University of California - Berkeley