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 AbstractRelationship between male moths of Cryptoblabes gnidiella (Milliere) (Lepidoptera: Pyralidae) caught in sex pheromone traps and cumulative degree-days in vineyards in southern Uruguay    Next AbstractPerfluorooctanoic acid and ammonium perfluorooctanoate: volatile surfactants for proteome analysis? »

J Phys Chem A


Title:Simplified Protocol for the Calculation of Multiconformer Transition State Theory Rate Constants Applied to Tropospheric OH-Initiated Oxidation Reactions
Author(s):Viegas LP;
Address:"Aarhus Institute of Advanced Studies, Aarhus University, Hoegh-Guldbergs Gade 6B, Buildings 1630-1632, Aarhus 8000, Denmark"
Journal Title:J Phys Chem A
Year:2021
Volume:20210426
Issue:21
Page Number:4499 - 4512
DOI: 10.1021/acs.jpca.1c00683
ISSN/ISBN:1520-5215 (Electronic) 1089-5639 (Linking)
Abstract:"Chemical kinetics plays a fundamental role in the understanding and modeling of tropospheric chemical processes, one of the most important being the atmospheric degradation of volatile organic compounds. These potentially harmful molecules are emitted into the troposphere by natural and anthropogenic sources and are chemically removed by undergoing oxidation processes, most frequently initiated by reaction with OH radicals, the atmosphere's 'detergent'. Obtaining the respective rate constants is therefore of critical importance, with calculations based on transition state theory (TST) often being the preferred choice. However, for molecules with rich conformational variety, a single-conformer method such as lowest-conformer TST is unsuitable while state-of-the-art TST-based methodologies easily become unmanageable. In this Feature Article, the author reviews his own cost-effective protocol for the calculation of bimolecular rate constants of OH-initiated reactions in the high-pressure limit based on multiconformer transition state theory. The protocol, which is easily extendable to other oxidation reactions involving saturated organic molecules, is based on a variety of freeware and open-source software and tested against a series of oxidation reactions of hydrofluoropolyethers, computationally very challenging molecules with potential environmental relevance. The main features, advantages and disadvantages of the protocol are presented, along with an assessment of its predictive utility based on a comparison with experimental rate constants"
Keywords:
Notes:"PubMed-not-MEDLINEViegas, Luis P eng 2021/04/28 J Phys Chem A. 2021 Jun 3; 125(21):4499-4512. doi: 10.1021/acs.jpca.1c00683. Epub 2021 Apr 26"

 
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 22-11-2024