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Reaction Mechanism of Organometallic Systems/ by Shahla Ilyas

By: Material type: TextTextPublication details: New Delhi: Oxford Book Company, 2022.Description: viii,264pISBN:
  • 9789391096724
Subject(s): DDC classification:
  • 541.39 ILY/R
Contents:
1.Rate Law and Mechanism-- 2.Principles of Chemical Dynamics-- 3.Steriochemical Change-- 4.Ligand Substitution Reactions-- 5.Oxidation -Reduction Reaction-- 6.Inorganic Photochemistry.
Summary: The study of Reaction Mechanism of Organometallic Systems is presented. The primary mechanistic types discussed are ligand substitution, oxidative addition, reductive elimination, and electron transfer. Each reaction pathway is discussed within the context of the common electron counts encountered for most organometallic complexes. Examples of how these common reaction pathways extend to polynuclear complexes are also presented. Although reasonable generalizations with regard to overall reaction rates and stepwise mechanisms using the electron count formalism can be made, many recent reports point out that the details of ligand and metal center structure can override these general trends. A considerable amount of quantitative rate data is provided and computational methodologies for understanding the observed rates are discussed.
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Holdings
Item type Current library Home library Call number Status Date due Barcode
Book Book Study Centre Alappuzha, University of Kerala Study Centre Alappuzha, University of Kerala 541.39 ILY/R (Browse shelf(Opens below)) Available USCA6166

1.Rate Law and Mechanism--
2.Principles of Chemical Dynamics--
3.Steriochemical Change--
4.Ligand Substitution Reactions--
5.Oxidation -Reduction Reaction--
6.Inorganic Photochemistry.

The study of Reaction Mechanism of Organometallic Systems is presented. The primary mechanistic types discussed are ligand substitution, oxidative addition, reductive elimination, and electron transfer. Each reaction pathway is discussed within the context of the common electron counts encountered for most organometallic complexes. Examples of how these common reaction pathways extend to polynuclear complexes are also presented. Although reasonable generalizations with regard to overall reaction rates and stepwise mechanisms using the electron count formalism can be made, many recent reports point out that the details of ligand and metal center structure can override these general trends. A considerable amount of quantitative rate data is provided and computational methodologies for understanding the observed rates are discussed.

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