Abstract

• The hybrid material (H 3 dien)[Ni(NO 3 )(C 2 O 4 ) 2 ].2H 2 O was synthesized using a soft chemistry route. • The crystal structure has been determined by X-ray single crystal diffraction. • Thermal behavior of title compound has been studied by TGA/DTA analysis. • The new compound turned to be an effective catalyst for the reduction reaction of the three nitrophenol isomers. • The negative Curie-Weiss temperature reveals antiferromagnetic coupling between the spin holders. The complex (H 3 dien)[Ni(NO 3 )(C 2 O 4 ) 2 ].2H 2 O, with (dien) is the diethylenetriamine (NH 2 CH 2 CH 2 ) 2 NH, and was synthesized in solution. It was characterized using single-crystal X-ray diffraction, Infrared (FT-IR) and UV-Visible spectroscopies, and TG-DTA thermal analysis. FT-IR confirmed the characteristic bands of diethylenetriamine, nitrate and oxalate groups. (H 3 dien)[Ni(NO 3 )(C 2 O 4 ) 2 ].2H 2 O crystallizes into the monoclinic system (P2 1 /c). Nickel has a square-based pyramidal NiO5 coordination. O-H...O and N-H...O H-bonds connect ionic entities and water molecules into bc -plane-parallel slabs. The UV-Visible spectrum shows absorption bands compatible with a six-coordinated high-spin octahedral Ni(II). Magnetization and a.c. susceptibility measurements were measured. The catalytic efficiency of the title compound in the reduction by NaBH4 of three nitrophenol isomers to their corresponding aminophenols was tested.

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