Lookup NU author(s): Dr Julie Parker,
Dr Katarina Novakovic
This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).
Reaction temperature plays a major role in product selectivity in the oscillatory mode of the palladium-catalyzed phe-nylacetylene oxidative carbonylation reaction. At 40 °C dimethyl (2Z)-2-phenyl-2-butenedioate is the major product whereas at 0 °C the major product is 5,5-dimethoxy-3-phenyl-2(5H)-furanone. The occurrence of oscillations in pH coincides with an increase in the rate of phenylacetylene consumption and associated product formation. Experiments were performed isothermally in a reaction calorimeter to correlate reactant consumption and product formation with the occurrence of pH oscillations and the heat released by the reaction. An increase in the size of the pH drop in a single oscillation correlates with an increase in energy, indicating that this section of a single oscillation relates to reactant consumption. Based on these observations a reaction pathway responsible for product formation is provided.
Author(s): Parker J, Novakovic K
Publication type: Article
Publication status: Published
Print publication date: 05/08/2017
Online publication date: 26/05/2017
Acceptance date: 24/05/2017
Date deposited: 30/06/2017
ISSN (print): 1439-4235
ISSN (electronic): 1439-7641
Data Source Location: http://dx.doi.org/10.17634/082584-1
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