Hydrolysis of phosphotriesters: Determination of transition states in parallel reactions by heavy-atom isotope effects

Citation
Ma. Anderson et al., Hydrolysis of phosphotriesters: Determination of transition states in parallel reactions by heavy-atom isotope effects, J AM CHEM S, 123(38), 2001, pp. 9246-9253
Citations number
57
Categorie Soggetti
Chemistry & Analysis",Chemistry
Journal title
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
ISSN journal
00027863 → ACNP
Volume
123
Issue
38
Year of publication
2001
Pages
9246 - 9253
Database
ISI
SICI code
0002-7863(20010926)123:38<9246:HOPDOT>2.0.ZU;2-B
Abstract
The remote label method was used to measure primary and secondary O-18 isot ope effects in the alkaline hydrolysis of O,O-diethylphosphorylcholine iodi de (DEPC) and the primary O-18 effect in the alkaline hydrolysis of O,O-die thyl-m-nitrobenzyl phosphate (DEmNBP). Both the leaving group of interest ( choline or m-nitrobenzyl alcohol) and ethanol can be ejected during hydroly sis due to the similarity of their pK values. The heavy-atom isotope effect s were measured by isotope ratio mass spectrometry. Parallel reaction and i ncomplete labeling corrections were made for both systems. DEPC has a prima ry O-18 isotope effect of 1.041 +/- 0.003 and a secondary O-18 isotope effe ct of 1.033 +/- 0.002. The primary O-18 isotope effect for DEmNBP was 1.052 +/- 0.003. These large effects suggest a highly associative transition sta te in which the nucleophile approaches very close to the phosphorus atom to eject the leaving group. The large values are also indicative of a large c ompression, or general movement, on the reaction coordinate.