Effects of Aminocarboxylate Ligands of Surface Active Copper(II) Complexes on the Hydrolysis of p-Nitrophenyldiphenylphosphate
β Scribed by C.P Ship; A Zainudin; Y.Y Lim
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 59 KB
- Volume
- 217
- Category
- Article
- ISSN
- 0021-9797
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β¦ Synopsis
The rate of hydrolysis of p-nitrophenyldiphenylphosphate in the presence of micellized [Cu(C 12 tmed)(L)] Ψ where C 12 tmed is N,N,N-trimethyl-N-dodecylethylenediamine and L is the anion part of the amino acid has been investigated. It was found that the observed maximum rate obtained under the excess surfactant over the substrate condition depends very much on the ability of the amino acid ligand to form a mixed-chelate complex with the [Cu(C 12 tmed)] 2Ψ moiety. In general, a chelating ligand with better coordination ability gives a slower rate because of the reduction in the supply of Cu-OH nucleophile in the micelle.
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The ternary complex kinetic model for metallomicellar catalysis has been proposed in this paper. The catalytic effects of bivalent metal ion (Cu(2+), Zn(2+), and Ni(2+)) complexes of long alkyl pyridine ligands upon the hydrolysis of p-nitrophenyl picolinate (PNPP) have been studied kinetically in a
## Abstract Two new bis(N,Oβbidentate) Schiff base ligands with asymmetric spacers between the donor sites have been synthesized. The asymmetric ligand H~2~L^1^ selfβassembles with copper(II) ions to give rise to a dinuclear copper(II) complex [Cu~2~L^1^~2~] (1), while a more flexible ligand H~2~L^