Published August 2019 | Version v1
Journal article

Two difunctional Co(II) coordination polymers for natural sunlight photocatalysis of methylene blue and selective fluorescence sensing of Cr(VI) ion in water media

  • 1. College of Chemical Engineering, Hebei Key Laboratory for Environment Photocatalytic and Electrocatalytic Materials, North China University of Science and Technology, No. 21 Bohai Road, Caofeidian New-city, Tangshan, Hebei, 063210 (China)

Description

Highlights: • Two new Co(II)-based CPs were synthesized and characterized. • 1–2 could serve as energy-saving photocatalysts for degrading MB under natural sunlight irradiation. • 1 exhibited highly sensitive and selective sensing for Cr(VI) anion. • The fluorescence quenching mechanisms were discussed. -- Abstract: Two new difunctional Co(II) coordination polymers (CPs), namely, [Co(TBTA)(L)1.5]n (1) and {[Co(NPHT)(L)]·H2O}n (2) were hydrothermally synthesized from 4,4′-bis(imidazole-1-yl)-biphenyl and different aromatic carboxylic acid ligands (H2TBTA = tetrabromoterephthalic acid, and H2NPHT = 3-nitrophthalic acid). Two CPs feature 2D (3,6)-connected hcb, and (4,4)-connected sql topologies for 1, and 2, respectively. 1 further extends into a three dimensional supramolecular architecture through π···π stacking interactions. Both of CPs exhibit high photocatalytic activities for degradation of methylene blue (MB) with remarkable efficiencies (85.83% for 1, and 93.76% for 2) under natural sunlight irradiation. 1 can sensitively and selectively detect Cr(VI) anions in water media with the Stern-Volmer quenching constant (Ksv) of 4.79 × 104 M−1 for Cr2O72− (pH = 3) or 2.36 × 104 M−1 for CrO42− (pH = 12). The linear detection ranges are 0–350 μM, and 0–200 μM for Cr2O72−, and for CrO42−, severally.

Additional details

Identifiers

DOI
10.1016/j.jssc.2019.05.025;
PII
S0022459619302543;

Publishing Information

Journal Title
Journal of Solid State Chemistry (Print)
Journal Volume
276
Journal Page Range
p. 331-338
ISSN
0022-4596
CODEN
JSSCBI

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Copyright
Copyright (c) 2019 Elsevier Inc. All rights reserved.