Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractRapid quantification of clove (Syzygium aromaticum) and spearmint (Mentha spicata) essential oils encapsulated in a complex organic matrix using an ATR-FTIR spectroscopic method    Next Abstract"Stereospecificity of an enzymatic monoene 1,4-dehydrogenation reaction: conversion of (Z)-11-tetradecenoic acid into (E,E)-10,12-tetradecadienoic acid" »

Chemistry


Title:Revealing structural effects: electrochemical reactions of butanols on platinum
Author(s):Rodriguez JL; Souto RM; Fernandez-Merida L; Pastor E;
Address:"Departamento de Quimica Fisica Universidad de La Laguna 38071 La Laguna, Tenerife, Spain"
Journal Title:Chemistry
Year:2002
Volume:8
Issue:9
Page Number:2134 - 2142
DOI: 10.1002/1521-3765(20020503)8:9<2134::AID-CHEM2134>3.0.CO;2-C
ISSN/ISBN:0947-6539 (Print) 0947-6539 (Linking)
Abstract:"Spectroelectrochemical studies on the reactivity of butanol isomers on Pt electrodes in perchloric acid medium led to the observation of structural effects that result from the different arrangements of atoms in the organic molecules. The use of differential electrochemical mass spectrometry (DEMS) to detect volatile products showed that all four isomers react on the electrode, though different product yields were observed for each compound. In spite of the differences in the electrochemical behaviour of the butanol isomers, a series of general processes accounts for the results obtained. The formation of strongly adsorbed residues by a dehydration process leading to the formation of a C=C bond was proposed for all isomers. Electroreduction of the adsorbates produces C(4) and C(3) alkanes, and the latter reveal the existence of a fragmentation process. The C(4) hydrocarbons can be formed by hydrogenation of these residues and by hydrogenolysis of alcohol molecules in the bulk solution which react at the electrode with adsorbed hydrogen. On the other hand, CO(2) is formed during electrooxidation of the adsorbed species. Partial-oxidation products containing a carbonyl group were detected from 0.2 M solutions of 1-butanol, isobutyl alcohol and sec-butyl alcohol. The tertiary alcohol tert-butyl alcohol only reacts in its adsorbed state"
Keywords:
Notes:"PubMed-not-MEDLINERodriguez, Jose L Souto, Ricardo M Fernandez-Merida, Luis Pastor, Elena eng Germany 2002/05/01 Chemistry. 2002 May 3; 8(9):2134-42. doi: 10.1002/1521-3765(20020503)8:9<2134::AID-CHEM2134>3.0.CO; 2-C"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 25-11-2024