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 AbstractComparative biochemical analysis during the anaerobic digestion of lignocellulosic biomass from six morphological parts of Williams Cavendish banana (Triploid Musa AAA group) plants    Next AbstractChemical composition of Cystoseira crinita Bory from the Eastern Mediterranean »

J Phys Chem A


Title:OH radical-initiated chemistry of isoprene in aqueous media. Atmospheric implications
Author(s):Kameel FR; Hoffmann MR; Colussi AJ;
Address:"Ronald and Maxine Linde Center for Global Environmental Science, California Institute of Technology , California 91125, United States"
Journal Title:J Phys Chem A
Year:2013
Volume:20130607
Issue:24
Page Number:5117 - 5123
DOI: 10.1021/jp4026267
ISSN/ISBN:1520-5215 (Electronic) 1089-5639 (Linking)
Abstract:"The fate of isoprene (2-methyl-1,3-butadiene, ISO) emissions into the atmosphere is not fully understood. Increasing awareness that ISO is only partially processed in the gas-phase has turned attention to its reactive uptake by fog, cloud, and aerosol droplets. A hydrophobic gas, ISO would preferentially partition to the surface rather than the bulk of aqueous media. Such media normally contain dissolved O2 and water-soluble unsaturated organics and support *OH generation rates (from the solar photolysis of dissolved H2O2) that are several orders of magnitude larger than in the gas-phase. Thus, ISO should be converted therein to heavier products rather than into the C4-C5 volatile compounds produced in the gas-phase. Here we substantiate such a scenario by reporting that the lambda > 305 nm photolysis of H2O2 in dilute aqueous ISO solutions yields C10H15OH species as primary products, whose formation both requires and is inhibited by O2. A minimum of seven C10H15OH isomers are resolved by reverse-phase high-performance liquid chromatography and detected as MH(+) (m/z = 153) and MH(+)-18 (m/z = 135) signals by electrospray ionization mass spectrometry. Our findings are consistent with the addition of *OH to ISO, followed by HO-ISO* reactions with ISO in competition with O2, leading to second generation HO(ISO)2* radicals that terminate as C10H15OH via beta-H abstraction by O2. We show that a significant fraction of gas-phase olefins should be converted into less volatile species via this process on wet airborne particles"
Keywords:
Notes:"PubMed-not-MEDLINEKameel, F Rifkha Hoffmann, M R Colussi, A J eng 2013/05/24 J Phys Chem A. 2013 Jun 20; 117(24):5117-23. doi: 10.1021/jp4026267. Epub 2013 Jun 7"

 
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 05-11-2024