Literature DB >> 14570471

34S isotope effect on sulfate ester hydrolysis: mechanistic implications.

Benjamin T Burlingham1, Lisa M Pratt, Ernest R Davidson, Vernon J Shiner, Jon Fong, Theodore S Widlanski.   

Abstract

In this communication, we report the first determination of 34S kinetic isotope effects (KIEs) for the hydrolysis of sulfate monoesters. The method involves the conversion of the inorganic sulfate, acquired at partial extent of reaction, to SO2, followed by isotope ratio determination by mass spectrometry. The KIEs determined for p-nitrophenyl sulfate and p-acetylphenyl sulfate are 1.0154 (+/-0.0002) and 1.0172 (+/-0.0003), respectively. These results, together with previous peripheral 18O KIE values, are inconsistent with an associative mechanism. The isotope effect method we report should also prove useful for studying the mechanism of other sulfuryl group transfers, including sulfatase and sulfotransferase reactions, as well as sulfate hydrolyses under other conditions.

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Year:  2003        PMID: 14570471     DOI: 10.1021/ja0279747

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  3 in total

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Authors:  Subashree Iyer; Alvan C Hengge
Journal:  J Org Chem       Date:  2008-06-06       Impact factor: 4.354

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Journal:  Nat Commun       Date:  2019-10-07       Impact factor: 14.919

3.  Modeling the Alkaline Hydrolysis of Diaryl Sulfate Diesters: A Mechanistic Study.

Authors:  Klaudia Szeler; Nicholas H Williams; Alvan C Hengge; Shina C L Kamerlin
Journal:  J Org Chem       Date:  2020-04-30       Impact factor: 4.354

  3 in total

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