4.5 Article

Syntheses, structures and luminescent properties of five new Ag(I)-based coordination polymers

Journal

INORGANICA CHIMICA ACTA
Volume 557, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.ica.2023.121710

Keywords

Coordination polymer; Crystal structure; Ag(I); Luminescent property

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In this study, five Ag(I)-based coordination polymers were successfully synthesized under hydrothermal conditions. The structures and luminescent properties of these polymers were characterized, demonstrating their diverse structures and tunable luminescent colors.
In this work, five Ag(I)-based coordination polymers (CPs), namely, [Ag(HL)(H2L)]n (1), [Ag(HL)(2,2 '-bpy) (H2O)0.5] (2), [Ag(HL)(phen)(H2O)0.5] (3), {[Ag2(HL)2(4,4 '-bpy)(H2O)2]center dot H2O} (4) and [Ag(HL)(thpy)]n (5), were synthesized under hydrothermal conditions (H2L = 1-(3-carboxybenzyl)-1H-pyrazole-4-carboxylic acid, 2,2 '-bpy = 2,2 '-bipyridine, phen = 1,10-phenanthroline, 4,4 '-bpy = 4,4 '-bipyridine and thpy = 2-(2-thienyl) pyridine). These coordination polymers were characterized by single-crystal X-ray diffraction, elemental analyses, infrared spectroscopy, thermogravimetric analyses and powder X-ray diffraction. Compound 1 displays a one-dimensional (1D) chain structure which can be further extended into a three-dimensional (3D) supramolecular structure via intermolecular hydrogen bond. In compounds 2 and 3, the binuclear zero dimensional (0D) units are extended to 3D supramolecular frameworks by intermolecular hydrogen bond and 7C-7C stacking interaction. In compound 4, the 0D units constructed by HL- anions, 4,4 '-bpy and metal ions are expanded to form a two-dimensional (2D) supramolecular network. Compound 5 shows a different 2D supramolecular structure extended from 1D chain by intermolecular hydrogen bond. The results suggest that organic ligand plays a key role in the formation of the final structures. The solid-state luminescent properties of compounds 1-5 were studied in detail. The results show that the luminescent color of compounds 1-5 can be tunable by varying excitation wavelengths.

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