2007
DOI: 10.1016/j.inoche.2007.01.008
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Five and six-coordinate silicon complexes with an O,N,O′-chelating ligand derived from o-hydroxyacetophenone–N-(2-hydroxyethyl)imine

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Cited by 45 publications
(3 citation statements)
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“…This can be explained by the electronegative character of the phenyl-bound O1 and the carboxyl-type oxygen atom O2. The bond lengths Si1-N1 and Si-C (Table 1) are similar as in similar pentacoordinate silicon complexes [4,6,23].…”
Section: Chosupporting
confidence: 68%
See 1 more Smart Citation
“…This can be explained by the electronegative character of the phenyl-bound O1 and the carboxyl-type oxygen atom O2. The bond lengths Si1-N1 and Si-C (Table 1) are similar as in similar pentacoordinate silicon complexes [4,6,23].…”
Section: Chosupporting
confidence: 68%
“…Herein, we wanted to expand the available pentacoordinate silicon complexes to those containing the N-[(2-oxy-1-naphthyl)methylene]leucinato ligand. Previously published related silicon complexes contain Schiff base ligands derived from o-hydroxyacetophenone [4,23], salicyl aldehyde [5], acetylacetone [24,25], or o-hydroxynaphthyl aldehyde [6].…”
Section: Introductionmentioning
confidence: 99%
“…ese values are lower than the corresponding values for bulk CuCl 2 •2H 2 O and nano-CuCl 2 •2H 2 O and ceftriaxone. e data indicate that ceftriaxone ligand is more active than their metal complexes; this may be because the chelating ligands containing N and O donor atoms show wide biological activity through bonding to metal ions [64,65]. However, the synergetic effects of ceftriaxone and Cu ion may play an important function in the inhibition of bacterial growth after the complex decomposition.…”
Section: Antibacterial Activitymentioning
confidence: 99%