top of page
Search

Modular functionalization and hydrogel formation via red-shifted and self-reporting cycloaddition

  • Writer: Andreas Walther
    Andreas Walther
  • Mar 3, 2021
  • 1 min read

Read the full article here: Chem. Commun., 2021,57, 805

by S. Ludwanowski, D. Hoenders, K. Kalayci, H. Frisch, C. Barner-Kowollik, and A. Walther


We present a modularly applicable, red-shifted and self-reporting photodynamic covalent crosslinker, abbreviated qStyPy, that performs [2+2] cycloadditions upon irradiation with 470 nm in water. The rational design of qStyPy increases its hydrophilicity due to a permanent charge and features a broad emission in the far-red/near-infrared regime as a readout for the cycloadduct formation, rendering qStyPy suitable for biomedical applications.




Recent Posts

See All
A subwoofer separates chiral fibers

Read the full article here: Chem, 2023, DOI: 10.1016/j.chempr.2023.02.006 Aritra Sarkar and Andreas Walther The spatial organization of...

 
 
 

Comments


Archive
Search By Tags
Follow Us
  • Facebook Basic Square
  • X
  • LinkedIn Social Icon

© Andreas Walther - all rights reserved

bottom of page