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[摘要]：Single-labeled pyridylporphyrinDNA conjugates are reported as highly sensitive and selective spectroscopic sensors for mercury(II) ions in water. The effects of chemical structure (thymine versus adenine), number of nucleotides (monomer versus octamer), and porphyrin metalation (Zn versus free base) on the sensitivity and selectivity of mercury(II) detection are explored. The results indicated that pyridylporphyrin rather than the nucleobase plays a crucial role in mercury(II) sensing, because porphyrin conjugates with both adenosine and thymidine exhibited excellent mercury(II) detection. Mercury(II) recognition was shown in emission quenching, as well as in a redshift of the porphyrin Soret band absorption. The limit of detection (LOD, 3 sigma/slope) of zinc(II) pyridylporphyrin-5-oligodeoxythymidine (ZnPorT8) obtained by fluorescence quenching was calculated to be 21.14nM. Other metal cations (Zn2+, Cd2+, Pb2+, Mn2+, Ca2+, Ni2+, Mg2+, Fe2+, Cu2+, and Na+) did not interfere with the emission and absorption sensing of mercury(II). Free-base porphyrinoligothymine conjugate 2HPorT8 displayed similar sensitivity to ZnPorT8 but different selectivity. The results also implied that the sensing properties of porphyrindeoxythymidine conjugates could potentially be tuned by porphyrin metalation. |
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