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Reactivity of Coordinated Oximes

โœ Scribed by A. J. L. Pombeiro; V. Yu Kukushkin


Publisher
John Wiley and Sons
Year
2004
Weight
7 KB
Volume
35
Category
Article
ISSN
0931-7597

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

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Defense. Aherdeen Proving Ground. MD 21010-5425. USA K e y word5 organophosphinate, orgdnophosphonatc. harin, oxiiiieq ,icetylcholinesterasc. rexti\dtioii. pretrc'itment The comparative potency of oximes for reactivation of inhibited eel acetylcholinesterase (AChE) in vitro is dependent on the orga

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A kinetic study of the reactivity in the cleavage of pnitrophenyl acetate of a series of 2-pyridineoximes, 1ฯช4, and their complexes with Ni II , Zn II and Cu II is reported. Complexation of the oximic ligands leads to a remarkable increase in the acidity of the oximic group, following the order Cu I