University of Stirling
Publishes on Chemical Reaction Mechanisms, Chemical Synthesis and Analysis, Inorganic and Organometallic Chemistry. 442 papers and 28.4k citations.
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It is pointed out that translational and (overall) rotational motions provide the important entropic driving force for enzymic and intramolecular rate accelerations and the chelate effect; internal rotations and unusually severe orientational requirements are generally of secondary importance. The loss of translational and (overall) rotational entropy for 2 --> 1 reactions in solution is ordinarily on the order of 45 entropy units (e.u.) (standard state 1 M, 25 degrees C); the translational entropy is much larger than 8 e.u. (corresponding to 55 M). Low-frequency motions in products and transition states, about 17 e.u. for cyclopentadiene dimerization, partially compensate for this loss, but "effective concentrations" on the order of 10(8) M may be accounted for without the introduction of new chemical concepts or terms.
It can be useful to describe the Gibbs free energy changes for the binding to a protein of a molecule, A-B, and of its component parts, A and B, in terms of the "intrinsic binding energies" of A and B, DeltaG(A) (i) and DeltaG(B) (i), and a "connection Gibbs energy," DeltaG(s) that is derived largely from changes in translational and rotational entropy. This empirical approach avoids the difficult or insoluble problem of interpreting observed DeltaH and TDeltaS values for aqueous solutions. The DeltaG(i) and DeltaG(s) terms can be large for binding to enzymes and other proteins.
Mechanisms for Rate Accelerations and Specificity Intrinsic Binding Energy Transition-State Analogs Catalysis by Micelles and Activity Coefficients of Transition States
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTA primer for the Bema Hapothle. An empirical approach to the characterization of changing transition-state structuresWilliam P. JencksCite this: Chem. Rev. 1985, 85, 6, 511–527Publication Date (Print):December 1, 1985Publication History Published online1 May 2002Published inissue 1 December 1985https://pubs.acs.org/doi/10.1021/cr00070a001https://doi.org/10.1021/cr00070a001research-articleACS PublicationsRequest reuse permissionsArticle Views1102Altmetric-Citations475LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose Get e-Alerts