Nickel-Catalyzed Coordination Polymerization-Induced Self-Assembly of Helical Poly(aryl isocyanide)s

  • Sètuhn Jimaja
  • , Spyridon Varlas
  • , Yujie Xie
  • , Jeffrey C. Foster
  • , Daniel Taton
  • , Andrew P. Dove
  • , Rachel K. O'Reilly

Research output: Contribution to journalArticlepeer-review

47 Scopus citations

Abstract

The interest in helix-containing nanostructures is currently growing as a consequence of their potential applications in areas such as nanomedicine, nanomaterial design, chiral recognition, and asymmetric catalysis. Herein, we present a facile and tunable one-pot methodology to achieve chiral nano-objects. The nickel-catalyzed coordination polymerization-induced self-assembly (NiCCo-PISA) of helical poly(aryl isocyanide) amphiphilic diblock copolymers was realized and allowed access to various nano-object morphologies (spheres, worm-like micelles, and polymersomes). The helicity of the core block was confirmed via circular dichroism (CD) spectroscopy for all morphologies, proving their chiral nature. Small-molecule uptake by the spherical nanoparticles was investigated by encapsulating Nile Red into the core of the spheres and subsequent transfer into aqueous media. The presence of a CD signal for the otherwise CD-inactive dye proved the chiral induction effect of the nano-objects' helical core. This demonstrates the potential of NiCCo-PISA to prepare nanoparticles for applications in nanomaterials, catalysis, and recognition.

Original languageEnglish
Pages (from-to)226-232
Number of pages7
JournalACS Macro Letters
Volume9
Issue number2
DOIs
StatePublished - Feb 18 2020
Externally publishedYes

Funding

This work was supported by the European Union (SUSPOL-EJD 642671), ERC (grant number 615142), EPSRC, and the University of Birmingham. Dr R. Keogh (University of Birmingham) is thanked for SLS assistance.

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