4.5 Article

Self-adjusting coordination of carboxylate for constructing stable 4-con-nected tetrazolate porous frameworks with luminescence

Journal

INORGANICA CHIMICA ACTA
Volume 561, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.ica.2023.121852

Keywords

Metal-organic frameworks; Tetrazole; Zeolite; Structural diversity; Luminescence

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Here, a series of zinc tetrahedral tetrazolate frameworks (Zn-TTFs) are presented, and it is demonstrated that rotation of carboxyl group can generate structural diversity. Compound 3 exhibits a unique zeolite-like structure, while compound 4 shows both super acid and alkali resistance.
Herein, a series of zinc tetrahedral tetrazolate frameworks (Zn-TTFs) are presented. The reactions of Zn (NO3)2 center dot 6H2O with 5-amino-1H-tetrazole and pyromellitic acid assemble four different Zn-tetrazolate porous networks, namely [Zn2(atz)3(PMA)]center dot guest (1), [Zn2(atz)3.5(PMA)0.25]center dot guest (2), [Zn (atz)1.5(PMA)0.25]center dot guest (3), [Zn3(atz)3(PMA)(Thiourea)(CH3OH)]center dot guest (4), (atz = 5-amino-1H-tetrazole, PMA = pyromellitic acid), whose results demonstrate that rotation of carboxyl group can generate the structural diversity. Interestingly, compound 3 shows a zeolite frl net, while compound 4 exhibits simultaneously super acid and alkali resistance. The luminescent properties based on compound 3 have been studied in the solid state at room temperature, and all of them display lanthanide-based luminescence.

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