TY - JOUR
T1 - Synthesis, characterization, density functional theory calculations, and in vitro antibacterial activity of novel transition metal complexes containing an O3-tridentate amoxicillin-based Schiff base
T2 - A silver(II) complex as alternative against Pseudomonas aeruginosa resistant to amoxicillin
AU - Anacona, J. R.
AU - Loroño, Marcos
AU - Marpa, Daniela
AU - Ramos, Cesar
AU - Celis, Freddy
N1 - Publisher Copyright:
© 2020 John Wiley & Sons, Ltd.
PY - 2020/9/1
Y1 - 2020/9/1
N2 - Transition metal complexes containing an amoxicillin-based Schiff base (H2L, 3) obtained from the condensation of amoxicillin 1 with salicylaldehyde 2 were prepared. Spectroscopic and physicochemical techniques, namely, UV–visible, Fourier-transform infrared spectroscopy, 1H NMR, electron paramagnetic resonance, transmission electron microscopy, mass spectrometry, magnetic susceptibility, molar conductance, density functional theory (DFT) calculations, together with elemental and thermal analyses were used to characterize the synthesized complexes. Based on these studies, the general formulae [ML(H2O)3], where M = Mn 4, Ni 5, Zn 6, and [ML(H2O)], where M = Cu 7, Ag 8, were proposed for the complexes. The amoxicillin-based Schiff base ligand behaved as a dianionic O3-tridentate chelating agent. DFT studies and magnetic and spectral data revealed octahedral geometries for Mn, Ni, and Zn atoms and distorted tetrahedral geometries for Cu(II) and Ag(II) complexes. Synthesized compounds were tested for antibacterial activity by both agar disk diffusion method and the minimum inhibitory concentration. in vitro bacterial viability revealed that complex 5 had similar antibacterial activity as 1 against Staphylococcus aureus and Staphylococcus epidermidis, whereas Pseudomonas aeruginosa, resistant to amoxicillin, was sensitive to complex 8. The antibacterial activity of complex 8 could be attributed to its greater catalytic activity as shown by DFT calculations. Toxicity bioassay of the tested compounds showed LC50 values > 1000 ppm, indicating their nontoxicity against brine shrimp nauplii (Artemia salina).
AB - Transition metal complexes containing an amoxicillin-based Schiff base (H2L, 3) obtained from the condensation of amoxicillin 1 with salicylaldehyde 2 were prepared. Spectroscopic and physicochemical techniques, namely, UV–visible, Fourier-transform infrared spectroscopy, 1H NMR, electron paramagnetic resonance, transmission electron microscopy, mass spectrometry, magnetic susceptibility, molar conductance, density functional theory (DFT) calculations, together with elemental and thermal analyses were used to characterize the synthesized complexes. Based on these studies, the general formulae [ML(H2O)3], where M = Mn 4, Ni 5, Zn 6, and [ML(H2O)], where M = Cu 7, Ag 8, were proposed for the complexes. The amoxicillin-based Schiff base ligand behaved as a dianionic O3-tridentate chelating agent. DFT studies and magnetic and spectral data revealed octahedral geometries for Mn, Ni, and Zn atoms and distorted tetrahedral geometries for Cu(II) and Ag(II) complexes. Synthesized compounds were tested for antibacterial activity by both agar disk diffusion method and the minimum inhibitory concentration. in vitro bacterial viability revealed that complex 5 had similar antibacterial activity as 1 against Staphylococcus aureus and Staphylococcus epidermidis, whereas Pseudomonas aeruginosa, resistant to amoxicillin, was sensitive to complex 8. The antibacterial activity of complex 8 could be attributed to its greater catalytic activity as shown by DFT calculations. Toxicity bioassay of the tested compounds showed LC50 values > 1000 ppm, indicating their nontoxicity against brine shrimp nauplii (Artemia salina).
KW - DFT calculations
KW - Pseudomonas aeruginosa
KW - amoxicillin-based Schiff base metal complexes
KW - antibacterial activity
KW - silver(II) complex containing an amoxicillin-based Schiff base
UR - http://www.scopus.com/inward/record.url?scp=85084853280&partnerID=8YFLogxK
U2 - 10.1002/aoc.5755
DO - 10.1002/aoc.5755
M3 - Artículo
AN - SCOPUS:85084853280
SN - 0268-2605
VL - 34
JO - Applied Organometallic Chemistry
JF - Applied Organometallic Chemistry
IS - 9
M1 - e5755
ER -