Add like
Add dislike
Add to saved papers

A colorimetric and fluorescent chemosensor for selective detection of Cu 2+ based on a new diarylethene with a benzophenone hydrazone unit.

A new photochromic diarylethene based on benzophenone hydrazone has been synthesized. Its photochromic and fluorescent properties changed upon alternating irradiation with UV/Vis light and adding Cu2+ /EDTA in methanol, which showed that the diarylethene could be served as a colorimetric and fluorescent chemosensor for selective detection of Cu2+ based on internal charge transfer processes. The colorimetric and turn-off fluorescent selective detection of Cu2+ was attributed to the 2:1 complex of the diarylethene and Cu2+ . The binding constant (Ka) was 1.53 × 104  L mol-1 and the limit of detection of the diarylethene for Cu2+ was calculated to be 1.45 × 10-6  mol L-1 . In addition, the metal-responsive photochromic behavior of diarylethene was applied successfully to the construction of a molecular logic circuit.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app