Abstract
A novel photochromic dye conjugate architecture is described, which allows both covalent tethering to a polymeric host matrix and fast photochromic switching. The new conjugates consist of a photochromic dye covalently bound to two different substituents via a Y-branching linker (hetero Y-branching), one being a polymerizable methacrylate moiety and the other a soft (low T g) poly(dimethylsiloxane) oligomer. The novel conjugates gave faster photochromic decoloration in the host lens matrix compared with the electronically equivalent nonmatrix-bound and unconjugated parent control dyes. In addition, further acceleration of fade speed kinetics was observed with a longer linker between photochromic dye and methacrylate moiety.
| Original language | English |
|---|---|
| Pages (from-to) | 476-486 |
| Number of pages | 11 |
| Journal | Journal of Polymer Science Part A: Polymer Chemistry |
| Volume | 49 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 15 Jan 2011 |
Keywords
- branched
- matrix
- photochromic dyes
- polydimethylsiloxane
- polysiloxanes
- tethering
- Y-branched