Literature DB >> 11747416

Formation and stability of carbocations and carbanions in water and intrinsic barriers to their reactions.

J P Richard1, T L Amyes, M M Toteva.   

Abstract

Lifetimes in water as short as 10(-11) s have been determined for carbocations and carbanions by referencing the rate of their reaction with solvent species to that for the appropriate "clock" reaction, and equilibrium constants have been determined as the ratio of rate constants for their formation and breakdown. Rate-equilibrium correlations for these organic ions are often poor and sometimes even defy the simple generalization that reactivity increases with decreasing stability. This seemingly confusing body of data can be understood through consideration of the both the Marcus intrinsic barrier and the thermodynamic driving force to reaction of these organic ions.

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Year:  2001        PMID: 11747416     DOI: 10.1021/ar0000556

Source DB:  PubMed          Journal:  Acc Chem Res        ISSN: 0001-4842            Impact factor:   22.384


  24 in total

Review 1.  The PLP cofactor: lessons from studies on model reactions.

Authors:  John P Richard; Tina L Amyes; Juan Crugeiras; Ana Rios
Journal:  Biochim Biophys Acta       Date:  2010-12-20

2.  Dynamics for Reactions of Ion Pairs in Aqueous Solution: Reactivity of Tosylate Anion Ion Paired with the Highly Destabilized 1-(4-Methylphenyl)-2,2,2-Trifluoroethyl Carbocation.

Authors:  Minami Teshima; Yutaka Tsuji; John P Richard
Journal:  J Phys Org Chem       Date:  2010-08-01       Impact factor: 2.391

3.  Proton transfer from C-6 of uridine 5'-monophosphate catalyzed by orotidine 5'-monophosphate decarboxylase: formation and stability of a vinyl carbanion intermediate and the effect of a 5-fluoro substituent.

Authors:  Wing-Yin Tsang; B McKay Wood; Freeman M Wong; Weiming Wu; John A Gerlt; Tina L Amyes; John P Richard
Journal:  J Am Chem Soc       Date:  2012-08-21       Impact factor: 15.419

4.  Formation and Mechanism for Reactions of Ring-Substituted Phenonium Ions in Aqueous Solution.

Authors:  Yutaka Tsuji; John P Richard
Journal:  J Phys Org Chem       Date:  2015-11-30       Impact factor: 2.391

Review 5.  Enzymatic rate enhancements: a review and perspective.

Authors:  John P Richard
Journal:  Biochemistry       Date:  2013-03-14       Impact factor: 3.162

6.  A Marcus treatment of rate constants for protonation of ring-substituted alpha-methoxystyrenes: intrinsic reaction barriers and the shape of the reaction coordinate.

Authors:  John P Richard; Kathleen B Williams
Journal:  J Am Chem Soc       Date:  2007-05-09       Impact factor: 15.419

Review 7.  Pyridoxal 5'-phosphate: electrophilic catalyst extraordinaire.

Authors:  John P Richard; Tina L Amyes; Juan Crugeiras; Ana Rios
Journal:  Curr Opin Chem Biol       Date:  2009-07-27       Impact factor: 8.822

8.  Substituent Effects on the Formation and Nucleophile Selectivity of Ring-Substituted Phenonium Ions in Aqueous Solution.

Authors:  Yutaka Tsuji; Shin Ogawa; John P Richard
Journal:  J Phys Org Chem       Date:  2013-12-01       Impact factor: 2.391

9.  The Generation and Reactions of Quinone Methides.

Authors:  Maria M Toteva; John P Richard
Journal:  Adv Phys Org Chem       Date:  2011-01-01       Impact factor: 2.833

10.  Enzymatic Catalysis of Proton Transfer and Decarboxylation Reactions.

Authors:  John P Richard
Journal:  Pure Appl Chem       Date:  2011-07-08       Impact factor: 2.453

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