Synthesis, crystal structure and bioactivities of Schiff base derived from paeonol and 1,4-bis(3-aminopropy) piperazine

A new Schiff base, paeonol-[1,4-bis (3-aminopropyl) piperazine], was synthesized for the first time by the condensation reaction of paeonol and 1,4-bis (3-aminopropyl) piperazine through solution method. The product was characterized by the methods of melting point, IR, UV-vis, fluorescence spectrum, 1H NMR, elemental and thermal analysis, and its crystal structure was analyzed by single crystal X-ray diffraction method, which indicated that it belongs to triclinic system, p-1 group, a = 6.836(14) Å,b = 7.729(17) Å,c = 12.28(3) Å, α = 87.25(2)°,β = 85.53(2)°,γ = 88.74(2)°. The antioxidant and in vitro antibacterial activities of the product were investigated by DPPH· method and agar plate diffusion method, respectively. Moreover, the interaction of the product with biomacromolecule DNA was studied by the electronic spectroscopy and viscosity method.

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Publication Details

Journal
Журнал структурной химии
Published
2024-10-17
DOI
https://doi.org/10.26902/jsc_id139311
Primary Topic
Crystal structures of chemical compounds
Type
article
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article

Synthesis, crystal structure and bioactivities of Schiff base derived from paeonol and 1,4-bis(3-aminopropy) piperazine

Tieqi Xu, Hai-Lun Wan, Cheng Wang, Min Gao et al.
Журнал структурной химии
Crystal structures of chemical compounds
article

Synthesis, crystal structure and bioactivities of Schiff base derived from paeonol and 1,4-bis(3-aminopropy) piperazine

Tieqi Xu, Hai-Lun Wan, Cheng Wang, Min Gao, Rongman Xu, Yijiao Huang
article en

Abstract

A new Schiff base, paeonol-[1,4-bis (3-aminopropyl) piperazine], was synthesized for the first time by the condensation reaction of paeonol and 1,4-bis (3-aminopropyl) piperazine through solution method. The product was characterized by the methods of melting point, IR, UV-vis, fluorescence spectrum, 1H NMR, elemental and thermal analysis, and its crystal structure was analyzed by single crystal X-ray diffraction method, which indicated that it belongs to triclinic system, p-1 group, a = 6.836(14) Å,b = 7.729(17) Å,c = 12.28(3) Å, α = 87.25(2)°,β = 85.53(2)°,γ = 88.74(2)°. The antioxidant and in vitro antibacterial activities of the product were investigated by DPPH· method and agar plate diffusion method, respectively. Moreover, the interaction of the product with biomacromolecule DNA was studied by the electronic spectroscopy and viscosity method.

Журнал структурной химииVol. 66(1)
Clean water and sanitation
Openalex Percentile: Top 86%
Crystal structures of chemical compounds
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