biostudies-literatureUnknown7(47)Nasaruddin NHA Schiff base bearing two methyl substituents, namely, 6,6'-((1<i>E</i>,1'<i>E</i>)-((2,2-dimethylpropane-1,3-diyl) bis(azanylylidene)) bis(methanylylidene)) bis(2-methylphenol) [H₂AD1Me] was synthesized and characterized through physicochemical and spectroscopic analyses. Then, the Schiff base was complexed with Pd(II) and Ni(II) to form [Pd(AD1Me)] and [Ni(AD1Me)], respectively. Both metal complexes were successfully obtained and characterized through several analyses, <i>viz</i>., melting point, elemental analysis, molar conductivity, magnetic susceptibility, FTIR, ¹H NMR, UV-vis, and single crystal X-ray diffraction. A quantitative analysis of the intermolecular interactions in the crystal structures has been performed using Hirshfeld surface analysis. Both metal complexes were crystallized in a monoclinic crystal system with the space group of <i>P</i>2₁/<i>c</i>. Additionally, the deprotonated phenolic oxygen atom (O1/O2) and azomethine nitrogen atom (N1/N2) of the ligand chelate the Pd(II) and Ni(II) ions, forming a slightly distorted square-planar complex containing three six-membered rings encircling the metal core with dsp² hybridization. The shift of ν(C=N) to a higher frequency in FTIR by 26-28 cm^-1 indicated that the complexation to Pd(II) and Ni(II) through the azomethine N was established. It was further supported through the shifting of the azomethine proton signal to higher or lower chemical shifts with Δδ = 0.43-1.15 ppm in ¹H NMR. In addition, the shifting of the n-π*(C=N) band in UV-vis spectra with Δλ = 24-40 nm indicated the involvement of azomethine nitrogen in the complexation. All the compounds showed no significant antibacterial activity against three bacterial strains, namely, <i>Staphylococcus aureus</i> subsp. <i>aureus</i> Rosenbach (ATCC 6538), <i>Streptococcus mutans</i> Clarke (ATCC 700,610), and <i>Proteus vulgaris</i> (ATCC 6380), as the percent growth inhibition calculated was less than 90%.ACS omega42809-42818https://www.ebi.ac.uk/biostudies/studies/S-EPMC9713794biostudies-literatureSynthesis, Structural Characterization, Hirshfeld Surface Analysis, and Antibacterial Study of Pd(II) and Ni(II) Schiff Base Complexes Derived from Aliphatic Diamine.PMC9713794Zakaria NAMohamad Nazam SSSirat SSRahman NMMAMohd Yusof NSAhmad SNTan KWBahron HNasaruddin NHfalseSynthesis, Structural Characterization, Hirshfeld Surface Analysis, and Antibacterial Study of Pd(II) and Ni(II) Schiff Base Complexes Derived from Aliphatic Diamine.A Schiff base bearing two methyl substituents, namely, 6,6'-((1<i>E</i>,1'<i>E</i>)-((2,2-dimethylpropane-1,3-diyl) bis(azanylylidene)) bis(methanylylidene)) bis(2-methylphenol) [H₂AD1Me] was synthesized and characterized through physicochemical and spectroscopic analyses. Then, the Schiff base was complexed with Pd(II) and Ni(II) to form [Pd(AD1Me)] and [Ni(AD1Me)], respectively. Both metal complexes were successfully obtained and characterized through several analyses, <i>viz</i>., melting point, elemental analysis, molar conductivity, magnetic susceptibility, FTIR, ¹H NMR, UV-vis, and single crystal X-ray diffraction. A quantitative analysis of the intermolecular interactions in the crystal structures has been performed using Hirshfeld surface analysis. Both metal complexes were crystallized in a monoclinic crystal system with the space group of <i>P</i>2₁/<i>c</i>. Additionally, the deprotonated phenolic oxygen atom (O1/O2) and azomethine nitrogen atom (N1/N2) of the ligand chelate the Pd(II) and Ni(II) ions, forming a slightly distorted square-planar complex containing three six-membered rings encircling the metal core with dsp² hybridization. The shift of ν(C=N) to a higher frequency in FTIR by 26-28 cm^-1 indicated that the complexation to Pd(II) and Ni(II) through the azomethine N was established. It was further supported through the shifting of the azomethine proton signal to higher or lower chemical shifts with Δδ = 0.43-1.15 ppm in ¹H NMR. In addition, the shifting of the n-π*(C=N) band in UV-vis spectra with Δλ = 24-40 nm indicated the involvement of azomethine nitrogen in the complexation. All the compounds showed no significant antibacterial activity against three bacterial strains, namely, <i>Staphylococcus aureus</i> subsp. <i>aureus</i> Rosenbach (ATCC 6538), <i>Streptococcus mutans</i> Clarke (ATCC 700,610), and <i>Proteus vulgaris</i> (ATCC 6380), as the percent growth inhibition calculated was less than 90%.2022-01-01T00:00:00Z2022 Nov2025-04-21T16:41:32.456Z2025-04-21T16:41:32.456ZS-EPMC97137943646790810.1021/acsomega.2c04688