Related Experiment Video
Updated: Jun 21, 2026

Controlling the Size, Shape and Stability of Supramolecular Polymers in Water
Published on: August 2, 2012
The effects of a complexing agent on the transverse stability of cubic autocatalytic reaction fronts
1Department of Applied Mathematics, University of Leeds, Leeds, LS2 9JT, United Kingdom. amtjhm@maths.leeds.ac.uk
Abstract:
The effects of adding a complexing agent on the propagation and transverse stability of reaction fronts in a system based on cubic autocatalysis is considered. Adding the complexing agent is seen to reduce the propagation speed, alter the reaction dynamics and the concentration of the final reaction product of the propagating reaction fronts. A linear stability analysis (LSA) is considered to determine how the complexing agent affects the stability of planar reaction fronts through the numerical calculation of dispersion curves, plots of the growth rate sigma against wavenumber k. These dispersion curves show that adding the complexing agent can make the system unstable when it would otherwise be stable and, when the system is diffusionally unstable without the complexing agent, weaken this instability. An analysis valid for small values of k is undertaken, which confirms the results from the LSA and indicates how the critical value D(c) of the diffusion coefficient ratio D for the onset of an instability is changed by the addition of the complexing agent.
Related Concept Videos
Complexation Equilibria: Factors Influencing Stability of Complexes
Complexation Equilibria: The Chelate Effect
Stability of Equilibrium Configuration
A stable equilibrium occurs when a system tends to return to its original position when given a small displacement, and the potential energy is at its minimum. An example of a stable equilibrium is when a cantilever beam is fixed at one end and a weight is attached to the other end. If the weight...
Complexation Equilibria: Overview
The equilibrium constant of the complexation reaction is represented as the formation constant...
Stability of Substituted Cyclohexanes
The two chair conformations of cyclohexanes undergo rapid interconversion at room temperature. Both forms have identical energies and stabilities, each comprising equal amounts of the equilibrium mixture. Replacing a hydrogen atom with a functional group makes the two conformations energetically non-equivalent.
For example, in...
Radical Reactivity: Steric Effects
Along with electronic factors, steric factors also account...
![Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-(phosphinetriyl)tripiperidine]}palladium Under Mild Reaction Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F51444.jpg&w=3840&q=50)
