1991
DOI: 10.1007/bf01127877
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Schiff base complexes of zirconium(IV) derived from Zr(acac)4

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Cited by 10 publications
(5 citation statements)
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“…The zirconium ion of Schiff base Zr complexes are generally in oxidation state (IV) due to its high charge-to-size ratio (Z 2 ⁄r = 22.22 e 2 m -10 ) [116,117], and used for their catalytic properties. For instance, the dinuclear stable light yellow Zr(IV) complex 1 (Fig.…”
Section: Pentadentate Schiff Base Zr(iv) Complexesmentioning
confidence: 99%
“…The zirconium ion of Schiff base Zr complexes are generally in oxidation state (IV) due to its high charge-to-size ratio (Z 2 ⁄r = 22.22 e 2 m -10 ) [116,117], and used for their catalytic properties. For instance, the dinuclear stable light yellow Zr(IV) complex 1 (Fig.…”
Section: Pentadentate Schiff Base Zr(iv) Complexesmentioning
confidence: 99%
“…The Zr(iv) complex 2 was prepared from Zr(acac) 4 and the ligand H 2 sae according to a known procedure. 11 Recrystallisation of 2 from hot toluene produced crystals suitable for X-ray analysis. Complex 2 crystallises in a centrosymmetric dimeric form, 2-2, with the inversion centre in between the two zirconium atoms held together via two oxygens of the aminoethanolato-sidechains.…”
mentioning
confidence: 99%
“…Fragmentation also revealed the loss of Me-CO and Ar-CO from their chemical structures. A good physico chemical evidence for the presence of enolic and or ketonic tautomers of compounds I and III was deduced from free solubility of their Ar-NHCO derivatives in aqueous NaOH which confirm that the enolization forms take place towards aryl and or phenyl groups (Mishra et al, 1991).…”
Section: Journal Of Bioanalysis and Biomedicine -Open Accessmentioning
confidence: 82%
“…Both carbonyl compounds I-IV having a second carbonyl at b -position, are termed as b diketones. In general hydrogen bonding is possible only in syn form and not in anti form, where the orientation of enolization is towards the aryl or phenyl groups (Mishra et al, 1991) indicating the high enolic content of 4-aryl-1,3-diketones and not in 4-methyl-1,3diketones.…”
Section: Journal Of Bioanalysis and Biomedicine -Open Accessmentioning
confidence: 99%
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