2002
DOI: 10.1016/s0277-5387(02)01097-5
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Study of the interaction of oxovanadium(IV) with a plant component (caffeic acid). Synthesis and characterization of a solid compound

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Cited by 17 publications
(14 citation statements)
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“…In this case, and also at pH 12, a complex of composition Na 3 [VO(caf)(OH) 2 ]Á3H 2 O can be isolated in which the acid interacts with the oxocation through the two deprotonated OHgroups of the cetecholate-like part of the ligand [46]. On the other hand, potentiometric titrations complemented with the measurement of electronic spectra suggested the presence of some other species in solution, at different pH-values [46].…”
Section: Vo 2+ Complexes Of Quinic Acidmentioning
confidence: 82%
“…In this case, and also at pH 12, a complex of composition Na 3 [VO(caf)(OH) 2 ]Á3H 2 O can be isolated in which the acid interacts with the oxocation through the two deprotonated OHgroups of the cetecholate-like part of the ligand [46]. On the other hand, potentiometric titrations complemented with the measurement of electronic spectra suggested the presence of some other species in solution, at different pH-values [46].…”
Section: Vo 2+ Complexes Of Quinic Acidmentioning
confidence: 82%
“…It is evident ( Figure 1, Table 1), that the absorption at 1645 cm −1 disappears for samples of CA/CeO2 with a lower concentration of CA, while this band appears at lower frequencies (1645-1632 cm −1 ). Literature data on the assignment of the absorption at 1645 cm −1 for СА [39,[41][42][43][44] differ. It was attributed [43] to the stretching vibrations of the double bonds C=C.…”
Section: Fourier Transform-infrared (Ft-ir) Spectroscopy Of Caffeic Amentioning
confidence: 93%
“…Literature data on the assignment of the absorption at 1645 cm −1 for СА [39,[41][42][43][44] differ. It was attributed [43] to the stretching vibrations of the double bonds C=C. However, most researchers attribute this band to νС=O [39,41,42,44].…”
Section: Fourier Transform-infrared (Ft-ir) Spectroscopy Of Caffeic Amentioning
confidence: 93%
“…The obtained values of pK a1 and pK a2 are in good agree- ment with those reported in literatures. [26][27][28][29][34][35][36][37] As shown in Fig. 1, the pK a1 of ligands C and D occurs in the carboxylic group, followed by the dissociation of hydroxyl group at the para-position (pK a2 ).…”
Section: Resultsmentioning
confidence: 96%