Abstract
A dinuclear ruthenium(II) complex linked via a reducible azo group [Ru(bpy)2(azobpy)Ru(bpy)2]Cl4 (Ru 2azo, bpy = 2,2′-bipyridine, azobpy = 4,4″-azobis (2,2′-bipyridine)) was adopted as a probe for thiols. Results showed that Ru2azo could selectively and effectively react with biological thiols (such as cysteine, homocysteine and glutathione) with a 10- 7 M detection limit. After it reacted with thiols, the original gray color of Ru2azo solution immediately turned yellow and the luminescence significantly enhanced, showing "naked-eye" colorimetric and "off-on" luminescent dual-signaling response for thiols. Mechanism studies demonstrated that Ru2azo reacted with thiols undergoing a two-electron transfer process, forming the azo2 - anion product.
| Original language | English |
|---|---|
| Pages (from-to) | 108-113 |
| Number of pages | 6 |
| Journal | Journal of Inorganic Biochemistry |
| Volume | 121 |
| DOIs | |
| State | Published - Apr 2013 |
| Externally published | Yes |
Keywords
- Azo
- Biological thiols
- Chemosensor
- Redox reaction
- Ruthenium(II) complex
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