Abstract
A novel efficient luminescent chemosensor based on a 1,4,7,10-tetraazacyclododecane (cyclen)-tethered Ru(bpy)3(2+) derivative (Ru-cyclen) has been synthesized and characterized. It displays an ON-OFF-type luminescence change with excellent selectivity towards Cu(II) amongst 16 metal ions in 100% aqueous solution. The binding stoichiometry of Ru-cyclen with Cu(2+) was established by Job plot analysis and mass spectral evidence. Furthermore, the in situ generated Ru-cyclen-Cu ensemble recovered luminescence in the presence of S(2-), indicating an 'OFF-ON'-type sensing process. Similar phenomena were not observed with other common anions and biothiols, making it a high selective sulfide probe. Finally, the sensing mechanism is confirmed to be displacement approach by NMR, mass and emission spectrometry.
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