ROMPISA: Ring-Opening Metathesis Polymerization-Induced Self-Assembly

Daniel B. Wright, Mollie A. Touve, Lisa Adamiak, Nathan C. Gianneschi*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

107 Scopus citations

Abstract

Herein we report a polymerization-induced self-assembly (PISA) process with ring-opening metathesis polymerization (ROMP). We utilize a peptide-based norbornenyl monomer as a hydrophobic unit to provide a range of nanostructures at room temperature yet at high solids concentrations of 20 wt % in combination with an oligoethylene glycol based norbornenyl monomer. Evaluation of the polymerizations under mild conditions highlight that good control is maintained along with high monomer conversion of greater than 99%, indicating that the living polymerization is unaffected during the PISA process. The demonstration broadens the scope of the PISA process to a new living polymerization methodology toward the development of easily accessible and highly functionalized nanostructures in situ.

Original languageEnglish (US)
Pages (from-to)925-929
Number of pages5
JournalACS Macro Letters
Volume6
Issue number9
DOIs
StatePublished - Sep 19 2017

Funding

This research was conducted with Government support under and awarded by DoD through a MURI from the Air Force Office of Scientific Research (FA-9550-16-1-0150) and a National Defense Science and Engineering Graduate (NDSEG) Fellowship, 32 CFR 168a. We acknowledge the use of the UCSD Cryo-Electron Microscopy Facility, which is supported by NIH grants to Dr. Timothy S. Baker and a gift from the Agouron Institute to UCSD. Dr. Matthew Thompson is kindly thanked for preparing the OEG norbornene monomer and Grubbs’ 3rd generation catalyst.

ASJC Scopus subject areas

  • Organic Chemistry
  • Polymers and Plastics
  • Inorganic Chemistry
  • Materials Chemistry

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