Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
177242 | Dyes and Pigments | 2011 | 5 Pages |
Abstract
A new photochromic diarylethene 2a is synthesized and undergoes excellent ring-opening and ring-closing photoisomerization with UV/Vis light irradiation. The absorption of ring-closing isomer 2b (λmax = 615 nm, in dichloromethane) is found to match well with the fluorescence emission of dye 1 (λem = 610, ϕf = 0.76, in dichloromethane). By mixture of 1 and 2a in the ratio of 1:2.5 equiv., a simple and efficient fluorescence switching system is built. The fluorescence intensity of 1 is modulated easily with the photoisomerization of diarylethene 2a/2b by controlling irradiation time. With detecting fluorescence change, a readout method for multi-level optical storage is demonstrated.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
Huan-Huan Liu, Yi Chen,