How does quenching a reaction work
The first mechanism is based upon an unsuccessful hydrogen atom transfer and may occur through two different direct and stepwise routes. The second mechanism is based on an unsuccessful charge transfer reaction that occurs exclusively in a direct fashion.
We show that the efficiency of the two quenching mechanisms is substantially due to the existence of two different types of conical intersections between the excited and ground state potential energy surfaces of the reacting bimolecular system. Sinicropi, W. Nau and M. Olivucci, Photochem. To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.
If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given. If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. Read more about how to correctly acknowledge RSC content.
Fetching data from CrossRef. This may take some time to load. Loading related content. Jump to main content. Jump to site search.
You do not have JavaScript enabled. Please enable JavaScript to access the full features of the site or access our non-JavaScript page. Monitoring a kinetic reaction is straight-forward, provided that the reaction does not proceed to a appreciable extent during the time it takes to make an individual measurement. As you might expect, this requirement places a serious limitation on a kinetic method of analysis.
One solution to this problem is to stop, or quench the reaction by adjusting experimental conditions. For example, many reactions show a strong pH dependency, and may be quenched by adding a strong acid or a strong base. The illustration below shows a typical example for the enzymatic analysis of p -nitrophenylphosphate using the enzyme wheat germ acid phosphatase to hydrolyze the analyte to p -nitrophenol.
The reaction has a maximum rate at a pH of 5. Increasing the pH by adding NaOH quenches the reaction and converts the colorless p -nitrophenol to the yellow-colored p -nitrophenolate, which absorbs at nm. See author's posts. Your email address will not be published.
Save my name, email, and website in this browser for the next time I comment.
0コメント