2021
DOI: 10.1016/j.ica.2021.120557
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Synthesis, structural characterisation and antibacterial activities of lead(II) and some transition metal complexes derived from quinoline-2-carboxaldehyde 4-methyl-3-thiosemicarbazone

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Cited by 25 publications
(3 citation statements)
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“…2-butyl thioquinazoline-4-(3 H )-thiosemicarbazone ( 86 ) was added to Co(II), Ni(II), and Cu(II) salts in refluxing ethanol reflux for 3–4 h, and the reaction afforded 2-butyl thioquinazoline-4-(3 H )-thiosemicarbazone complexes 87a – h in 60–65% yields [ 97 ] ( Scheme 43 ). These complexes were also subjected to study their antimicrobial screening against, Gram-positive bacteria Candida albicans and Gram-negative bacteria Escherichia coli by disc diffusion technique [ 97 ].…”
Section: Metal Complexes Of Thiosemicarbazones and Thiocarbazonesmentioning
confidence: 99%
“…2-butyl thioquinazoline-4-(3 H )-thiosemicarbazone ( 86 ) was added to Co(II), Ni(II), and Cu(II) salts in refluxing ethanol reflux for 3–4 h, and the reaction afforded 2-butyl thioquinazoline-4-(3 H )-thiosemicarbazone complexes 87a – h in 60–65% yields [ 97 ] ( Scheme 43 ). These complexes were also subjected to study their antimicrobial screening against, Gram-positive bacteria Candida albicans and Gram-negative bacteria Escherichia coli by disc diffusion technique [ 97 ].…”
Section: Metal Complexes Of Thiosemicarbazones and Thiocarbazonesmentioning
confidence: 99%
“…[1][2][3] The most striking biological properties include anti tumorous, antioxidant, antibacterial, antifungal, anticancerogenic,besides showing insulinmimeticeffects. [4][5][6][7][8][9][10][11][12] thiosemicarbazones exist in thione and thienol forms both in solution and solid state, most strikingly thione form stays in solution phase.…”
Section: Introductionmentioning
confidence: 99%
“…The most common one is as N,S bidentate chelate [3,4], coordination mode that affords the formation of a very stable five-membered chelate ring, but many others are described in the literature, for example S monodentante [5,6], N,S bidentate chelate and S bridge [7,8] Crystals 2022, 12, 310 2 of 12 or N,S bidentate chelate and N bridge [9]. This, together with the control of protonation/deprotonation and the nature of auxiliary anions, lead to the formation of different structures such as monomers [10][11][12], dimers [13][14][15] or coordination polymers [16][17][18]. In addition to their fascinating structural properties, TSCs have a wide range of applications in different fields as catalysis [19][20][21], metal detoxification [22][23][24], metal sensing [25][26][27] or medicine [28][29][30][31].…”
Section: Introductionmentioning
confidence: 99%