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 AbstractCucurbitacin B Activates Bitter-Sensing Gustatory Receptor Neurons via Gustatory Receptor 33a in Drosophila melanogaster    Next AbstractDiacetyl levels and volatile profiles of commercial starter distillates and selected dairy foods »

Rapid Commun Mass Spectrom


Title:Chemical ionization by [NO]+ and subsequent collision-induced dissociation for the selective on-line detection of monoterpenes and linalool
Author(s):Rimetz-Planchon J; Dhooghe F; Schoon N; Vanhaecke F; Amelynck C;
Address:"Belgian Institute for Space Aeronomy, Ringlaan, Brussels, Belgium"
Journal Title:Rapid Commun Mass Spectrom
Year:2011
Volume:25
Issue:5
Page Number:647 - 654
DOI: 10.1002/rcm.4901
ISSN/ISBN:1097-0231 (Electronic) 0951-4198 (Linking)
Abstract:"Existing on-line Chemical Ionization Mass Spectrometry (CIMS) techniques for quantification of atmospheric trace gases, such as Biogenic Volatile Organic Compounds (BVOCs), suffer from difficulty in discriminating between isomeric (and more generally isobaric) compounds. Selective detection of these compounds, however, is important because they can affect atmospheric chemistry in different ways, depending on their chemical structure. In this work, Flowing Afterglow Tandem Mass Spectrometry (FATMS) was used to investigate the feasibility of the selective detection of a series of monoterpenes, an oxygenated monoterpene (linalool) and a sesquiterpene (beta-caryophyllene). Ions at m/z 137 from [H(3)O](+) chemical ionization of alpha-pinene, linalool and beta-caryophyllene have been subjected to Collision-Induced Dissociation (CID) with Ar in the collision cell of a tandem mass spectrometer at center-of-mass energies ranging between 0 and 8 eV. Similar fragmentation patterns were obtained, demonstrating that this method is not suited for the selective detection of these compounds. However, CID of the ions at m/z 136 produced via [NO](+) chemical ionization of a series of monoterpenes has revealed promising results. Some tracer-product ions for individual compounds or groups of compounds were found, which can be considered as a step forward towards selective on-line monitoring of BVOCs with CIMS techniques"
Keywords:Acyclic Monoterpenes Monoterpenes/*chemistry Nitric Oxide/*chemistry Sensitivity and Specificity Tandem Mass Spectrometry/*methods;
Notes:"MedlineRimetz-Planchon, Juliette Dhooghe, Frederik Schoon, Niels Vanhaecke, Frank Amelynck, Crist eng Research Support, Non-U.S. Gov't England 2011/02/05 Rapid Commun Mass Spectrom. 2011 Mar 15; 25(5):647-54. doi: 10.1002/rcm.4901"

 
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 16-11-2024