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Helical polymer self-assembly and chiral nanostructure formation

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POLYMER CHEMISTRY
卷 12, 期 13, 页码 -

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d0py01558j

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Significant advances have been made in the field of chiral helical polymers, with emergent properties of chiral nanoobjects derived from self-assembly and potential for new functional devices. Lessons from natural systems provide parallels and opportunities for further development in the field.
Since the pioneering efforts of Nolte, Okamoto and Green, the field of chiral helical polymers has made significant inroads. Here, we review recent advances made in the design, production and implementation of helical polymer systems. We examine the corresponding chiral nanoobjects derived from their self-assembly and detail their emergent properties as well as their potentials for the construction of new functional devices. We further note parallels and lessons to be learned from natural systems and discuss new directions and opportunities. Principles of homochiral evolution and hierarchical structuring derived from systematic study are presented. With a particular emphasis on methods for the controlled generation of chiral structures of predefined size and morphology, we review recent efforts to apply polymerization induced self-assembly (PISA) and crystallization driven self-assembly (CDSA) to helical polymers. Material properties including circularly polarized luminescence (CPLu), chemosensory detection, chiral discrimination, multi-stimuli responsiveness, chiral plasmonics, and magnetic and magneto-optical behaviours are discussed.

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