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 AbstractSodium chloride primes JA-independent defense against Spodoptera litura (Fabricius) larvae in Arabidopsis thaliana    Next Abstract"Unsaturated cuticular hydrocarbons synergize responses to sex attractant pheromone in the yellow peach moth, Conogethes punctiferalis" »

J Phys Chem A


Title:Quantum Chemical Investigation on Photochemical Reactions of Nonanoic Acids at Air-Water Interface
Author(s):Xiao P; Wang Q; Fang WH; Cui G;
Address:"Key Laboratory of Theoretical and Computational Photochemistry, Ministry of Education, College of Chemistry, Beijing Normal University , Beijing 100875, China"
Journal Title:J Phys Chem A
Year:2017
Volume:20170524
Issue:22
Page Number:4253 - 4262
DOI: 10.1021/acs.jpca.7b03123
ISSN/ISBN:1520-5215 (Electronic) 1089-5639 (Linking)
Abstract:"Photoinduced chemical reactions of organic compounds at the marine boundary layer have recently attracted significant experimental attention because this kind of photoreactions has been proposed to have substantial impact on local new particle formation and their photoproducts could be a source of secondary organic aerosols. In this work, we have employed first-principles density functional theory method combined with cluster models to systematically explore photochemical reaction pathways of nonanoic acids (NAs) to form volatile saturated and unsaturated C(9) and C(8) aldehydes at air-water interfaces. On the basis of the results, we have found that the formation of C(9) aldehydes is not initiated by intermolecular Norrish type II reaction between two NAs but by intramolecular T(1) C-O bond fission of NA generating acyl and hydroxyl radicals. Subsequently, saturated C(9) aldehydes are formed through hydrogenation reaction of acyl radical by another intact NA. Following two dehydrogenation reactions, unsaturated C(9) aldehydes are generated. In parallel, the pathway to C(8) aldehydes is initiated by T(1) C-C bond fission of NA, which generates octyl and carboxyl radicals; then, an octanol is formed through recombination reaction of octyl with hydroxyl radical. In the following, two dehydrogenation reactions result into an enol intermediate from which saturated C(8) aldehydes are produced via NA-assisted intermolecular hydrogen transfer. Finally, two dehydrogenation reactions generate unsaturated C(8) aldehydes. In these reactions, water and NA molecules are found to play important roles. They significantly reduce relevant reaction barriers. Our work has also explored oxygenation reactions of NA with molecular oxygen and radical-radical dimerization reactions"
Keywords:
Notes:"PubMed-not-MEDLINEXiao, Pin Wang, Qian Fang, Wei-Hai Cui, Ganglong eng 2017/05/18 J Phys Chem A. 2017 Jun 8; 121(22):4253-4262. doi: 10.1021/acs.jpca.7b03123. Epub 2017 May 24"

 
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