4.7 Article

Luminescent lanthanide metal-organic frameworks for chemical sensing and toxic anion detection

Journal

DALTON TRANSACTIONS
Volume 46, Issue 30, Pages 9859-9867

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7dt01790a

Keywords

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Funding

  1. National Natural Science Foundation of China [21403097]
  2. Fundamental Research Funds for the Central Universities [lzujbky-2016-45]

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Prototype lanthanide metal-organic frameworks (LnMOFs), Ln(BTC) (Ln = Eu and Tb; BTC = benzene-1,3,5- tricarboxylate), have been considered as luminescent sensors for detecting toxic anions, while their neutral pore structures have limited the entrance and encapsulation of anions to produce highly anion-responsive photoluminescence (PL). To facilitate anions to enter the pore space of Ln(BTC), a one-pot synthesis method was proposed in which BTC was partially replaced with its structural analogue L.BF4 (H3L.BF4 = 2,4,6-tricarboxy-1-methylpyridinium tetrafluoroborate) which consists of an anion affinity site of cationic methylpyridinium. Compared to the original Ln(BTC), the co-doped cationic framework Eu0.05Tb0.95-BTC0.9L0.1 is highly sensitive for detecting different toxic anions by tuning the energy absorption of organic chromophores, the energy transfer efficiency to Ln(3+) ions and the energy allocation between different Ln(3+) ions in the PL spectra. We demonstrated that the Eu0.05Tb0.95-BTC0.9L0.1 PL sensor has the capability of decoding various toxic anions with a clearly differentiable and unique emission intensity ratio of D-5(4) -> F-7(5) (Tb3+, 545 nm) to D-5(0) -> F-7(2) (Eu3+, 618 nm) transitions (/T-b/I-Eu). Compared to Ln(BTC), the co-doped Eu0.05Tb0.95-BTC0.9L0.1 presents self-calibrating, high distinguishable and stable PL signals for detecting toxic anions.

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