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 AbstractStructural and Chemical Profiles of Myrcia splendens (Myrtaceae) Leaves Under the Influence of the Galling Nexothrips sp. (Thysanoptera)    Next AbstractOlfactory and quantitative analysis of aroma compounds in elder flower (Sambucus nigra L.) drink processed from five cultivars »

J Phys Chem A


Title:Rapid Hydrogen Shift Scrambling in Hydroperoxy-Substituted Organic Peroxy Radicals
Author(s):Jorgensen S; Knap HC; Otkjaer RV; Jensen AM; Kjeldsen ML; Wennberg PO; Kjaergaard HG;
Address:"Department of Chemistry, University of Copenhagen , Universitetsparken 5, 2100 Copenhagen O, Denmark. Division of Geological and Planetary Sciences and Division of Engineering and Applied Science, California Institute of Technology , 1200 E. California Blvd., Pasadena, California 91125, United States"
Journal Title:J Phys Chem A
Year:2016
Volume:20160112
Issue:2
Page Number:266 - 275
DOI: 10.1021/acs.jpca.5b06768
ISSN/ISBN:1520-5215 (Electronic) 1089-5639 (Linking)
Abstract:"Using quantum mechanical calculations, we have investigated hydrogen shift (H-shift) reactions in peroxy radicals derived from the atmospheric oxidation of 1-pentene (CH2 horizontal lineCHCH2CH2CH3) and its monosubstituted derivatives. We investigate the peroxy radicals, HOCH2CH(OO)CR1HCH2CH3, HOCH2CH(OO)CH2CR1HCH3, and HOCH2CH(OO)CH2CH2CR1H2, where the substituent R1 is an alcoholic (OH), a hydroperoxy (OOH), or a methoxy (OCH3) group. For peroxy radicals with an OOH substituent, the H-shift reaction from the hydrogen atom on the OOH group to the OO group is extremely fast. We find that the rate constants of this type of H-shift reactions are greater than 10(3) s(-1) for both the forward and the reverse reactions. It leads to the formation of two different radical isomers that react through different reaction mechanisms and yield different products. These very fast H-shift reactions are much faster than the reactions with NO and HO2 under most atmospheric conditions and must be included in the atmospheric modeling of volatile organic compounds where hydroperoxy peroxy radicals are formed"
Keywords:
Notes:"PubMed-not-MEDLINEJorgensen, Solvejg Knap, Hasse C Otkjaer, Rasmus V Jensen, Annesofie M Kjeldsen, Mette L H Wennberg, Paul O Kjaergaard, Henrik G eng Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. 2015/12/17 J Phys Chem A. 2016 Jan 21; 120(2):266-75. doi: 10.1021/acs.jpca.5b06768. Epub 2016 Jan 12"

 
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 18-11-2024