skip to main content


Search for: All records

Creators/Authors contains: "Scheutz, Georg M."

Note: When clicking on a Digital Object Identifier (DOI) number, you will be taken to an external site maintained by the publisher. Some full text articles may not yet be available without a charge during the embargo (administrative interval).
What is a DOI Number?

Some links on this page may take you to non-federal websites. Their policies may differ from this site.

  1. We describe the photoinduced intrachain crosslinking of coumarin-containing copolymers in various organic solvents. Analysis of copolymer solvation and comparison to a molecular coumarin derivative revealed solvophobicity-driven crosslinking kinetics and chain compaction that facilitated the synthesis of single-chain nanoparticles. 
    more » « less
  2. Polymerization-induced self-assembly (PISA) is a facile method to obtain block copolymer aggregates with defined morphologies. However, the transitions between these morphologies have been difficult to monitor directly in real-time during the polymerization. Herein, we describe a straightforward and readily accessible in situ method to monitor the evolution of nanostructure via changes in internal hydrophobicity during the PISA process using a polymer-tethered pyrene fluorescent probe. We were able to correlate morphological transitions with changes of the pyrene emission and gain unprecedented insight into the evolution of core hydrophobicity during PISA. 
    more » « less
  3. null (Ed.)
    We describe a self-catalyzing photoredox polymerization system for the modular generation of macromolecular photocatalysts. Specifically, we designed a photoactive eosin Y-derived monomer that can induce photoelectron/energy transfer, while simultaneously partaking in reversible addition–fragmentation chain transfer polymerization as a monomer, affording polymer catalysts with tunable eosin Y incorporations. 
    more » « less
  4. null (Ed.)
  5. null (Ed.)
  6. null (Ed.)
    We report the one-step synthesis of diversely substituted functional 1,2-dithiolanes by reacting readily accessible 1,3-bis- tert -butyl thioethers with bromine. The reaction proceeds to completion within minutes under mild conditions, presumably via a sulfonium-mediated ring closure. Using X-ray crystallography and UV-vis spectroscopy, we demonstrate how substituent size and ring substitution pattern can affect the geometry and photophysical properties of 1,2-dithiolanes. 
    more » « less
  7. null (Ed.)