4.8 Article

Azobenzene Photoswitching without Ultraviolet Light

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 133, Issue 49, Pages 19684-19687

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja209239m

Keywords

-

Funding

  1. Natural Sciences and Engineering Research Council of Canada
  2. Ontario Graduate Scholarship

Ask authors/readers for more resources

Most azobenzene-based photoswitches use UV light for photoisomerization. This can limit their application in biological systems, where UV light can trigger unwanted responses, including cellular apoptosis. We have found that substitution of all four ortho positions with methoxy groups in an amidoazobenzene derivative leads to a substantial (similar to 35 rim) red shift of the n-pi* band of the trans isomer, separating it from the cis n-pi* transition. This red shift makes trans-to-cis photoswitching possible using green light (530-560 nm). The cis state is thermally stable with a half-life of similar to 2.4 days in the dark in aqueous solution. Reverse (cis-to-trans) photoswitching can be accomplished with blue light (460 rim), so bidirectional photoswitching between thermally stable isomers is possible without using UV light at all.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available