Abstract
The influence of adsorbed CO formed by dissociative chemisorption on the electrooxidation pathways and kinetics of 22 alcohols and aldehydes on polycrystalline platinum and palladium electrodes in relation to the adsorbed CO formed by dissociative chemisorption has been examined systematically by means of real-time sequences of FTIR spectra obtained during slow (2 mV s{sup {minus}1}) voltammetric sweeps in 0.1 M HClO{sub 4}. The overall objective is to explore the reactant structure-dependent role that adsorbed CO (and other CO{sub 2}-producing species) plays in the organic electrooxidation. The reactants examined include short-chain primary and secondary alcohols, aldehydes, and small bifunctional molecules (e.g., ethylene glycol) containing alcohol, aldehyde, and/or carboxylic acid units.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
