Interaction of heterocycles and nucleophiles: Sigma complexes formed from methoxide ion and some 5-nitropyrimidines and comparison with those from 2,4,6-trinitroanisole
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Published:1969
Issue:12
Volume:22
Page:2561
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ISSN:0004-9425
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Container-title:Australian Journal of Chemistry
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language:en
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Short-container-title:Aust. J. Chem.
Author:
Biffin MEC,Miller J,Moritz AG,Paul DB
Abstract
The sigma complexes formed
from the reaction of methoxide ion with 6- nitro-pyrimidine and its monomethoxy
derivatives have been examined spectroscopically. Structural ambiguities
resulting from the lower symmetry of the nitropyrimidines compared with the trinitrobenzenes
have been resolved by selective deuteration. Comparison is made with sigma
complex formation from 2,4,6-trinitroanisole and the question of kinetic
against thermodynamic control is considered with reference to theoretically
derived P.E.-reaction coordinate profiles for protic solvents. The calculations
are extended qualitatively to consider reactions in an aprotic solvent.
Publisher
CSIRO Publishing
Subject
General Chemistry
Cited by
29 articles.
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2. References;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02
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4. Solvent effect on the alkaline hydrolysis of 2-thiophenyl- 3,5-dinitropyridine;International Journal of Chemical Kinetics;2006
5. Additions of water, hydroxide ions, alcohols and alkoxide ions to carbonyl and azomethine bonds;Arkivoc;2002-09-01