Organometallic chemistry - Substitution reactions
Article REF: AF6502 V1

Organometallic chemistry - Substitution reactions

Author : Yves JEANNIN

Publication date: July 10, 2000, Review date: March 30, 2015 | Lire en français

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AUTHOR

  • Yves JEANNIN: Professor Emeritus at Pierre-et-Marie-Curie University - Correspondent of the French Academy of Sciences - Engineer from the École nationale supérieure de chimie de Paris (ENSCP)

 INTRODUCTION

The first step in building a bond between a transition metal atom and a carbon monoxide molecule is to donate the doublet carried by the carbon atom. The return of electron density from the transition metal to the carbon monoxide actually enables this doublet to be donated, as the carbon monoxide molecule is not a Lewis base.

It's only natural that if a molecule has free electron density in the form of a doublet, and if this molecule also has empty electron orbitals that can be donated in return, a substitution should take place. This is the subject of this article. Of course, this assumes that the orbital symmetries of the metal and the ligand molecule are compatible, so that overlap can take place. In other words, this means that the orbitals of the carbon monoxide and the molecule substituting it will have equivalent symmetries; they are known as isolobals. This concept will be further developed and used.

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