2012
DOI: 10.5562/cca2119
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Synthesis and Characterization of a Copper(II) Complex with 6-Hydroxypicolinic Acid and 3-Picoline

Abstract: Abstract.A copper(II) complex with 6-hydroxypicolinic acid (6-OHpicH) and 3-picoline (3-pic), [Cu(6-OHpic) 2 (3-pic) 2 ] (1), was prepared by recrystallization of [Cu(6-OHpic) 2 (H 2 O) 2 ] from 3-picoline and characterized by IR spectroscopy and thermal methods (TGA/DTA and DSC). The molecular and crystal structure of 1 was determined by single-crystal X-ray structural analysis. The copper(II) ion in 1 has a tetragonally compressed octahedral coordination environment, achieved by two N,O-bidentate 6-hydroxypi… Show more

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Cited by 9 publications
(4 citation statements)
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“…Peaks of medium intensity around 1580 cm À1 are assigned to m(C@N) of the coordinated ligand, in good agreement with the N,O-chelation [19,22]. The same coordination mode was observed in previous works for some complexes containing 3-HPA as ligands [18,19,[22][23][24]. The stretching vibrations of the uncoordinated hydroxyl group of ligand appear in the range 3448-3455 cm À1 .…”
Section: Resultssupporting
confidence: 83%
“…Peaks of medium intensity around 1580 cm À1 are assigned to m(C@N) of the coordinated ligand, in good agreement with the N,O-chelation [19,22]. The same coordination mode was observed in previous works for some complexes containing 3-HPA as ligands [18,19,[22][23][24]. The stretching vibrations of the uncoordinated hydroxyl group of ligand appear in the range 3448-3455 cm À1 .…”
Section: Resultssupporting
confidence: 83%
“…1.) revealed a one major decomposition step around 338 o C, associated with loss of organic moieties of the ligand leaving the residual weight corresponding to copper sulfide [14][15][16]. TEM, SEM and EDS studies of HDA-and TOPO-capped CuS nanocrystals are displayed in Fig.…”
Section: Resultsmentioning
confidence: 98%
“…The noteworthy difference between the inhibition efficiencies of SNBB on iron and copper must then relate to the coordination chemistry of these metals. The Cu + ion favors complex formation with carboxylic acid derivatives mainly through one of the oxygen atoms of the carboxylic functional group (η 1 -O2C-R) [58]. Moreover, considering the electroneutrality principle, further coordination of the second oxygen atom of the carboxylate group using a bidentate O, O-chelating mode is not a favorable process for Cu + , leaving it exposed to Clattack.…”
Section: Chemical Structure and Mechanism Of Corrosion Inhibitionmentioning
confidence: 99%