2014
DOI: 10.1039/c4nj00977k
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Co(ii), Ni(ii) and Cu(ii) complexes with phenylthiazole and thiosemicarbazone-derived ligands: synthesis, structure and cytotoxic effects

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Cited by 35 publications
(19 citation statements)
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(33 reference statements)
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“…The 1 H NMR, 13 C NMR, IR spectrals data was obtained for all new complexes 2a-2d and new ligand 1b, while ligands 1a, 1c and 1d were prepared by methods described in literature. 20,23,24 The chemical shis and intensities are compatible with products obtained in the synthesis procedure. Aromatic protons of pcymene were seen in the range from 4.71 to 6.16 ppm as doublets.…”
Section: Characterization Of Ligand 1b and Half-sandwich Complexes 2a-2dmentioning
confidence: 85%
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“…The 1 H NMR, 13 C NMR, IR spectrals data was obtained for all new complexes 2a-2d and new ligand 1b, while ligands 1a, 1c and 1d were prepared by methods described in literature. 20,23,24 The chemical shis and intensities are compatible with products obtained in the synthesis procedure. Aromatic protons of pcymene were seen in the range from 4.71 to 6.16 ppm as doublets.…”
Section: Characterization Of Ligand 1b and Half-sandwich Complexes 2a-2dmentioning
confidence: 85%
“…Ligands 1a, 1c and 1d were prepared with the use of methods described before. 20,23,24 The 1 H NMR and 13 C NMR spectra were registered in DMSO-d 6 (for all complexes) and CDCl 3 -d (for ligand 1b) using Bruker Avance III 600 MHz spectrometer. The IR spectra were recorded in KBr on the FTIR-8400S Shimadzu Spectrophotometer.…”
Section: Methodsmentioning
confidence: 99%
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“…In case of Co(II) complexes at higher temperature rapid spin lattice relaxation broadens lines [29]. The value for g||, g⊥ and giso are summarized in Table-2.…”
Section: Resultsmentioning
confidence: 99%