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Introduction to Enzyme Kinetics01:19

Introduction to Enzyme Kinetics

Enzyme kinetics studies the rates of biochemical reactions. Scientists monitor the reaction rates for a particular enzymatic reaction at various substrate concentrations. Additional trials with inhibitors or other molecules that affect the reaction rate may also be performed.
The experimenter can then plot the initial reaction rate or velocity (Vo) of a given trial against the substrate concentration ([S]) to obtain a graph of the reaction properties. For many enzymatic reactions involving a...
Effect of Temperature Change on Reaction Rate02:28

Effect of Temperature Change on Reaction Rate

The Arrhenius equation,
Predicting Reaction Outcomes02:24

Predicting Reaction Outcomes

Kinetics describes the rate and path by which a reaction occurs. In contrast, thermodynamics deals with state functions and describes the properties, behavior, and components of a system. It is not concerned with the path taken by the process and cannot address the rate at which a reaction occurs. Although it does provide information about what can happen during a reaction process, it does not describe the detailed steps of what appears on an atomic or a molecular level. On the other hand,...
Enzyme Kinetics01:19

Enzyme Kinetics

Enzymes speed up reactions by lowering the activation energy of the reactants. The speed at which the enzyme turns reactants into products is called the rate of reaction. Several factors impact the rate of reaction, including the number of available reactants. Enzyme kinetics is the study of how an enzyme changes the rate of a reaction.
Scientists typically study enzyme kinetics with a fixed amount of enzyme in the controlled environment of a test tube. When more reactant, or substrate, is...
Transition State Theory01:25

Transition State Theory

Transition-state theory, also known as activated-complex theory, provides a molecular-level explanation of reaction rates in both gas-phase and solution-phase reactions. It extends earlier kinetic models by considering the formation of a short-lived, high-energy configuration during a reaction.The progress of a chemical reaction can be represented using a reaction profile, which plots potential energy against the reaction coordinate. As two reactant molecules approach one another, their...
Free Energy and Equilibrium02:56

Free Energy and Equilibrium

The free energy change for a process may be viewed as a measure of its driving force. A negative value for ΔG represents a driving force for the process in the forward direction, while a positive value represents a driving force for the process in the reverse direction. When ΔGrxn is zero, the forward and reverse driving forces are equal, and the process occurs in both directions at the same rate (the system is at equilibrium).
Recall that Q is the numerical value of the mass action expression...

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Updated: Jul 15, 2026

Hot Biological Catalysis: Isothermal Titration Calorimetry to Characterize Enzymatic Reactions
13:00

Hot Biological Catalysis: Isothermal Titration Calorimetry to Characterize Enzymatic Reactions

Published on: April 4, 2014

Efecto cinético del beta-hidrógeno.

Raffaello Romeo1, Giuseppina D'Amico, Emilia Sicilia

  • 1Dipartimento di Chimica Inorganica, Chimica Analitica e Chimica Fisica, Università di Messina, Salita Sperone, 31-Vill. S. Agata-98166 Messina, Italy. rromeo@unime.it

Journal of the American Chemical Society
|April 6, 2007
PubMed
Resumen

Este estudio revela que los beta-hidrógenos aceleran la isomerización del complejo de platino a través de interacciones agósticas. Estas interacciones estabilizan los intermediarios, cruciales para la comprensión de la activación de alcano en la catálisis.

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Área de la Ciencia:

  • Química organometálica Química orgánica de los metales.
  • Química computacional es la química computacional.
  • La cinética de la reacción.

Sus antecedentes:

  • Los complejos catiónicos de platino se someten a isomerización de isómeros cis a trans.
  • El mecanismo de reacción implica la disociación del disolvente y la formación de productos intermedios.
  • El papel de los sustituyentes y las interacciones del disolvente no se entiende completamente.

Objetivo del estudio:

  • Para investigar la isomerización no catalizada de cis-[Pt(R')(S)(PR3)2]+ a los isómeros trans.
  • Para aclarar el mecanismo, incluidos los pasos y los intermedios que determinan la tasa.
  • Comprender la influencia de los beta-hidrógenos y las interacciones agósticas en las velocidades de reacción.

Principales métodos:

  • Experimentos cinéticos combinados y cálculos de la Teoría Funcional de la Densidad (DFT).
  • Análisis de las vías de reacción, estados de transición y estructuras intermedias.
  • Cuantificación de las energías de disociación y las barreras de activación.

Principales resultados:

  • La isomerización se produce a través de la pérdida de disolventes y de intermediarios en forma de T.
  • Los beta-hidrógenos aceleran significativamente la velocidad de reacción a través del efecto cinético del beta-hidrógeno.
  • DFT confirma una interacción agóstica Pt....eta2-HC en los intermediarios, estabilizándolos por 21-33 kJ mol-1.

Conclusiones:

  • Las interacciones agósticas juegan un papel clave en la estabilización de los intermediarios del complejo de platino.
  • Comprender estas interacciones es vital para controlar las vías de reacción, particularmente en la activación de alcano.
  • El efecto cinético beta-hidrógeno proporciona un mecanismo para acelerar estas reacciones.