Abstract
4,5-Diamino-1,8-naphthalimide (DNP)-based chemosensor H1 was designed and synthesized. Probe H1 specifically recognized Cu2+ ions in neutral aqueous solution. The capture of Cu2+ by the receptor resulted in deprotonation of the secondary amine conjugated to the 1,8-naphthalimide chromophore, so that the electron-donation ability of the "N" atom would be greatly enhanced; thus probe H1 showed a 50 nm red-shift in absorption (from 464 nm to 514 nm) and a large colorimetric response, it also exhibited an on-off fluorescent response. Specifically, H1 is a pH-independent sensor in the range of 6.0 to 12.0 and can be used as a probe for Cu2+ in strong basic conditions. These results opened up new possibilities for construction of red-shift colorimetric and fluorescent sensors.
| Original language | English |
|---|---|
| Pages (from-to) | 1299-1303 |
| Number of pages | 5 |
| Journal | Organic and Biomolecular Chemistry |
| Volume | 7 |
| Issue number | 7 |
| DOIs | |
| State | Published - 2009 |
| Externally published | Yes |
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