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

Further Successes of the Meisenheimer Model

* email and
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
PDF Full-text Download PDF Full-Text [300 KB, uploaded 4 May 2012 08:17 CEST]

Export to BibTeX |

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.

Appl. Sci. EISSN 2076-3417 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert