23 research outputs found

    Living Radical Polymerization by the RAFT Process - A Second Update

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    Stereoregular High-Density Bottlebrush Polymer and Its Organic Nanocrystal Stereocomplex through Triple-Helix Formation

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    We report the synthesis of a well-defined molecular bottlebrush polymer with stereoregular side chains (i.e., syndiotactic PMMA). The simultaneous control over the molecular weight, side-chain tacticity, and architecture allows the macromolecule to stereocomplex with the complementary linear stereoregular polymers (i.e., isotactic PMMAs) in controlled manners. By modulating the feed ratio of the complexing materials and chain length of the linear assembling component, a variety of crystalline materials with different sizes and morphologies, including discrete spherical nanoparticle, multiple-particle assembly, and cross-linked network structure, can be produced. Among these, uniformed sized, stable nanocrystals that exhibit temperature-induced solution assembly and disassembly properties can be derived from a combined process of PMMA triple-helix stereocomplex formation and polymer architecture-directed intramolecular crystallization. This work has established a new, facile synthetic protocol toward stimuli-responsive organic nanocrystals, which is applicable to the fabrication of a wide variety of functional crystal nanomaterials with practical applications

    Stereo specific cyclic poly(methyl methacrylate) and its topology-guided hierarchically controlled supramolecular assemblies

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    In this study, the stereocomplexation between a novel stereospecific cyclic vinyl polymer, that is, cyclic syndiotactic poly(methyl methacrylate) (st-PMMA), with the complementary linear isotactic (it-) PMMA was investigated. Surprising new insight into the effects of the topology (i.e., end groups), size, and tacticity of the assembling components on stereocomplex formation was obtained. Characterization of the stereocomplexes revealed that the self-assembly of cyclic st- PMMAs and linear it-PMMAs resulted in the formation of an unprecedented "polypseudorotaxane-type" supramolecular assembly. This stereocomplex exhibited remarkably different physical properties as compared to the conventional PMMA triple-helix stereocomplex as a result of the restricted topology imposed by the cyclic st-PMMA assembling component
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