Continuous addition kinetic elucidation: catalyst and reactant order, rate constant, and poisoning from a single experiment
Open Access
- 24 August 2023
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Chemical Science
- Vol. 14 (36) , 9970-9977
Abstract
Kinetic analysis of catalytic reactions is a powerful tool for mechanistic elucidation but is often challenging to perform, limiting understanding and therefore development of these reactions. Establishing order in a catalyst is usually achieved by running several reactions at different loadings, which is both time-consuming and complicated by the challenge of maintaining consistent run-to-run experimental conditions. Continuous addition kinetic elucidation (CAKE) was developed to circumvent these issues by continuously injecting a catalyst into a reaction, while monitoring reaction progress over time. For reactions that are mth order in a single yield-limiting reactant and nth order in catalyst, a plot of reactant concentration against time has a shape dependent only on the orders m and n. Therefore, fitting experimental CAKE data (using open access code or a convenient web tool) allows the reactant and catalyst orders, rate constant, and the amount of complete catalyst inhibition to be determined from a single experiment. Kinetic information obtained from CAKE experiments showed good agreement with the literature.Keywords
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Funding Information
- Natural Sciences and Engineering Research Council of Canada (RGPIN-04045-2017, RGPIN-05555-2019)
This publication has 36 references indexed in Scilit:
- Kinetic Profiling of Catalytic Organic Reactions as a Mechanistic ToolJournal of the American Chemical Society, 2015
- Deactivation in Homogeneous Transition Metal Catalysis: Causes, Avoidance, and CureChemical Reviews, 2014
- Kinetic Data for the Transmetalation/Reductive Elimination in Palladium‐Catalyzed Suzuki–Miyaura Reactions: Unexpected Triple Role of Hydroxide Ions Used as BaseChemistry – A European Journal, 2011
- Aryl Trifluoroborates in Suzuki–Miyaura Coupling: The Roles of Endogenous Aryl Boronic Acid and FluorideAngewandte Chemie International Edition, 2010
- Wash Bottle Laboratory Exercises: Iodide-Catalyzed H2O2 Decomposition Reaction Kinetics Using the Initial Rate ApproachJournal of Chemical Education, 2009
- Reaction Progress Analysis: Powerful Tool for Understanding Suzuki−Miyaura Reaction and Control of Polychlorobiphenyl ImpurityOrganic Process Research & Development, 2009
- Mechanisms of Catalyst Poisoning in Palladium-Catalyzed Cyanation of Haloarenes. Remarkably Facile C−N Bond Activation in the [(Ph3P)4Pd]/[Bu4N]+ CN- SystemJournal of the American Chemical Society, 2008
- Investigations of Pd-Catalyzed ArX Coupling Reactions Informed by Reaction Progress Kinetic AnalysisThe Journal of Organic Chemistry, 2006
- Reaction Progress Kinetic Analysis: A Powerful Methodology for Mechanistic Studies of Complex Catalytic ReactionsAngewandte Chemie International Edition, 2005
- Semi-automatic catalytic titration method for the analysis of cystine-cysteine mixtures and its application to urine samplesThe Analyst, 1988