Appl. Sci. 2012, 2(2), 443-452; doi:10.3390/app2020443
Article

Further Successes of the Meisenheimer Model

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Received: 5 April 2012; in revised form: 27 April 2012 / Accepted: 27 April 2012 / Published: 4 May 2012
(This article belongs to the Special Issue Organo-Fluorine Chemical Science)
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: Our simple Meisenheimer model for predicting the principal site for nucleophilic substitution in aromatic perfluorocarbons is further tested on a series of recently published reactions in liquid ammonia primarily from Malykhin and coworkers. The model accurately predicts the experimental results for all of the reactions reported further confirming its general applicability.
Keywords: nucleophilic substitution; fluorine-containing hetero-aromatics; Meisenheimer model
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MDPI and ACS Style

Baker, J.B.; Muir, M. Further Successes of the Meisenheimer Model. Appl. Sci. 2012, 2, 443-452.

AMA Style

Baker JB, Muir M. Further Successes of the Meisenheimer Model. Applied Sciences. 2012; 2(2):443-452.

Chicago/Turabian Style

Baker, Jon Baker; Muir, Max. 2012. "Further Successes of the Meisenheimer Model." Appl. Sci. 2, no. 2: 443-452.

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