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 AbstractInsect egg deposition renders plant defence against hatching larvae more effective in a salicylic acid-dependent manner    Next AbstractEvaluation of floral volatile patterns in the genus Narcissus using gas chromatography-coupled ion mobility spectrometry »

Chemphyschem


Title:Conformational Flexibility of Limonene Oxide Studied By Microwave Spectroscopy
Author(s):Loru D; Quesada-Moreno MM; Aviles-Moreno JR; Jarman N; Huet TR; Lopez-Gonzalez JJ; Sanz ME;
Address:"Department of Chemistry, King's College London, London, United Kingdom. University of Jaen, Department of Physical and Analytical Chemistry, Campus Las Lagunillas, E-23071, Jaen, Spain. PhLAM, UMR8523 CNRS-, Universite Lille 1, Batiment P5, F-59655, Villeneuve D'Ascq Cedex, France"
Journal Title:Chemphyschem
Year:2017
Volume:20161223
Issue:3
Page Number:274 - 280
DOI: 10.1002/cphc.201600991
ISSN/ISBN:1439-7641 (Electronic) 1439-4235 (Linking)
Abstract:"Monoterpenoids are biogenic volatile organic compounds that play a major role in atmospheric chemistry by participating in the formation of aerosols. In this work, the monoterpenoid (R)-(+)-limonene oxide (C(10) H(16) O) was characterized in the gas phase by Fourier-transform microwave spectroscopy in a supersonic jet. Five conformers of limonene oxide, four equatorial and one axial considering the configuration of the isopropenyl group, were unambiguously identified from analysis of the rotational spectrum. The observed conformers include cis and trans forms, which are stabilized by a subtle balance of hydrogen bonds, dispersive interactions, and steric effects. Estimated conformational relative abundances surprisingly reveal that the abundance of the axial conformer is similar to that of some of the equatorial conformers. In addition, the potential energy surface was extensively explored by using density functional theory and ab initio methods"
Keywords:Cyclohexane Monoterpenes *Microwaves Molecular Conformation Molecular Structure Monoterpenes/*chemistry Quantum Theory ab initio calculations atmospheric chemistry conformation analysis rotational spectroscopy terpenoids;
Notes:"MedlineLoru, Donatella Quesada-Moreno, Maria Mar Aviles-Moreno, Juan Ramon Jarman, Natasha Huet, Therese R Lopez-Gonzalez, Juan Jesus Sanz, M Eugenia eng Germany 2016/11/24 Chemphyschem. 2017 Feb 2; 18(3):274-280. doi: 10.1002/cphc.201600991. Epub 2016 Dec 23"

 
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 26-12-2024