2008
DOI: 10.1016/j.saa.2007.11.009
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Synthesis and structural investigation of mono- and polynuclear copper complexes of 4-ethyl-1-(pyridin-2-yl) thiosemicarbazide

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Cited by 57 publications
(62 citation statements)
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“…Also, two bands at 1512 and 1450 cm -1 were observed and assigned to thioamide I and III, respectively. Moreover, two sharp bands at 783 and 723 cm -1 were attributed to ν(C=S) and ρ(NH) [28]. The absence of any band due to ν(SH) in the range 2500 -2600 cm -1 [28] indicated that the ligand exists in the thione form.…”
Section: Characterization Of the Ligand (Hcpts)mentioning
confidence: 95%
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“…Also, two bands at 1512 and 1450 cm -1 were observed and assigned to thioamide I and III, respectively. Moreover, two sharp bands at 783 and 723 cm -1 were attributed to ν(C=S) and ρ(NH) [28]. The absence of any band due to ν(SH) in the range 2500 -2600 cm -1 [28] indicated that the ligand exists in the thione form.…”
Section: Characterization Of the Ligand (Hcpts)mentioning
confidence: 95%
“…The chemistry of these compounds was early explored [26] for their variable donor properties, structural diversity and biological applications. The coordination chemistry of a number of metal ions and a wide variety of complexes has been reported [27][28][29]. Thiosemicarbazides have been used for extraction and determination of some metal ions in biological and pharmacological samples [30][31][32].…”
Section: Introductionmentioning
confidence: 99%
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“…The infrared spectrum of N-ethyl-2-isonicotinoylhydrazinecarbothioamide (HEITsc), in comparison with that of, displayed three bands at 3275, 3253 and 3127 cm -1 attributed to ν(N 4 H), ν(N 2 H) and ν(N 1 H) vibrations [24], respectively. Also, four bands were displayed at 2977, 1674, 1640 and 1599 cm -1 and assigned to ν(CH) ali , ν(C=O) [25], ν(C=N) Py , and ν(C=C) Py [24] vibrations, respectively.…”
Section: Ir Spectramentioning
confidence: 99%
“…There are two main absorption bands in the spectra of the free ligand and their complexes; the first band is exhibited at the range 284 -308 nm and assigned to π-π* [31], and the second appeared at the range 330 -358 nm due to n-π* intraligand transitions [32]. These absorptions also present in the spectra of the Co(II), Cu(II) , Zn(II) and Sn(II) and [H 4 pClMaTS] ligand complexes, but they are shifted.…”
Section: Electronic Spectramentioning
confidence: 99%