Published February 2019 | Version v1
Journal article

4,5-Diamino-1,2-dihydropyridazine-3,6-dione-based layered Zn2+ coordination polymer and sensing properties on 2,4,6-trinitrophenol and Cr2O7 2

  • 1. College of Chemistry, and State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University, Changchun, Jilin, 130012 (China)

Description

Highlights: • Structure of acylhydrazide-based Zn2+ coordination polymer was reported. • Acylhydrazide originated from in situ acylation of organic acid with N2H4. • It can selectively sensing 2,4,6-trinitrophenol. • (vi) It can also selectively sensing Cr2O72-. -- Abstract: By employing the hydrothermal in situ acylation of organic acid with N2H4, we constructed a new acylhydrazidate-based Zn2+ coordination polymer [Zn2(apo)2]·H2O (H2(apo) = 4,5-diamino-1,2-dihydropyridazine-3,6-diol) 1. Interestingly, besides the acylation of 2,3-pyrazinedicarboxylic acid (pca) with N2H4, the breaking of partial C-(=)N bonds in the pyrazine ring also occurred, creating a new bridging-type acylhydrazide molecule H2(apo). In 1, the apo2- molecules exhibit a μ4 coordination mode, linking the tetrahedral Zn2+ centers into a 2-D layer network with a 44 topology. The photoluminescence analysis indicates that the title compound 1 emit the green light with the maximum at 490 nm upon excitation (λex = 380 nm, τ = 12.6 μs). Based on the better photoluminescence behavior of 1, the sensing ability of 1 on nitroaromatic explosives and inorganic anions were investigated. The results suggest that 1 can selectively detect 2,4,6-trinitrophenol (TNP) and Cr2O72-. This should be associated with the larger light adsorption at 380 nm for TNP and Cr2O72-. The light adsorption at 380 nm for the other nitroaromatic explosives and inorganic anions is weak.

Additional details

Identifiers

DOI
10.1016/j.jssc.2018.11.020;
PII
S0022459618305103;

Publishing Information

Journal Title
Journal of Solid State Chemistry (Print)
Journal Volume
270
Journal Page Range
p. 212-218
ISSN
0022-4596
CODEN
JSSCBI

Optional Information

Copyright
Copyright (c) 2018 Elsevier Inc. All rights reserved.