chemistry has been the introduction of transition metal catalysts to organic synthesis. Transition metal species can react with organic compounds to generate intermediates that contain carbon–metal bonds. Subsequent conversion of these organometallic intermediates could enrich the synthetic approach toward new molecules. Different from organocatalysis, the organometallic catalysis usually goes through multiple steps and complicated catalytic cycles, which originated from the complex bonding pattern of organometallic catalysts and the variation of valance state of the central metal species. Thus, the utilization of theoretical calculation for understanding the reaction mechanism is imperative for the development of organic chemistry. My post‐doctoral research with Professor K. N. Houk was working with experimental chemists to explore the mechanism of organometallic reactions through the collaboration of theoretical calculation with experimental study. The promotion of theoretical study on experimental development could be summarized into “3D,” i.e. description, design, and direction. Based on the data obtained from experimental study, detailed descriptions of the organometallic reaction mechanisms could be fulfilled using theoretical calculation. The mechanistic study then provides further theoretical guidance for the rational design of new reactions, which points out the direction of experimental development.
Over recent decades, massive experimental and theoretical investigations on organometallic catalysis have been reported. In those works, theoretical studies have been proved to be an indispensable technique for modern organic chemistry. Consequently, this book is written to summarize and generalize the theoretical advances in the mechanistic study of organometallic catalysis. This book comprises two parts, which are the general overview of organometallic catalysis and the computational studies of reaction mechanisms classified by transition metals. I hope this book could inspire the mechanistic studies of complex reactions for theoretical chemists, and enable a better understanding of reaction mechanisms for experimental chemists.
29 July 2020
Yu LanZhengzhou, P. R. China
Part I Theoretical View of Organometallic Catalysis
It is time to write a book on computational organometallic chemistry.
The first part of this book can be considered as the introduction to computational organometallic chemistry. It is a long history since organometallic catalysis has been applied in organic synthesis; however, the mechanism of those reactions is too complicated to understand. Indeed, computational chemistry provided a powerful tool to reveal the mechanism of organometallic reactions. During recent two decades, the combination of computational chemistry and organometallic chemistry has made a series of progress in mechanistic studies, which has led to a new discipline, computational organometallic chemistry.
The first part would be composed of three chapters. In Chapter 1, a brief history of organometallics is given to reveal the significance of this chemistry. Computational chemistry, especially computational methods, is discussed in Chapter 2, which would be used in mechanism study of organometallic catalysis. Detailed processes for the familiar elementary reactions in organometallic catalysis discovered by theoretical calculations are summarized in Chapter 3.
1 Introduction of Computational Organometallic Chemistry
This chapter provides a brief introduction of computational organometallic chemistry, which usually focuses on the reaction mechanism of homogeneous organometallic catalysis.
1.1 Overview of Organometallic Chemistry
In this section, the historical footprint of organometallic chemistry is concisely given, which would help the readers better understand the role of computation in the mechanistic study of organometallic chemistry.
1.1.1 General View of Organometallic Chemistry
Creating new material is always entrusted with the important responsibility for the development of human civilization [1–3]. In particular, synthetic chemistry becomes a powerful tool for chemists, as it exhibits great value for the selective construction of new compounds [4–8]. Various useful molecules could be prepared by the strategies of synthetic chemistry, which provides material foundation, technological support, and drive force for science [9–20]. Synthetic chemistry is also the motivating force for the progress of material science, pharmaceutical science, energy engineering, agriculture, and electronics industry [21–41]. In this area, organic synthesis reveals broad interests from a series of research fields, which could target supply to multifarious functional molecules.
The synthetic organic chemistry usually focuses on “carbon” to widen related research, which could afford various strategies for the building of molecular framework, functional group transformations, and controlling stereochemistry in more sophisticated molecules [9, 22, 42–50]. Therefore, selective formation of new covalent bond between carbon atom and some other atom involving nitrogen, oxygen, sulfur, halogen, boron, and phosphorus becomes one of the most important aims for synthetic organic chemistry. In particular, nucleophiles and electrophiles are important for the construction of new covalent bonds.
A nucleophile, which is a molecule with formal lone‐pair electrophiles, can donate two electrons to its reaction partner for the formation of new covalent bond. Alternatively, an electrophile, which is a molecule with formal unoccupied orbitals, can accept two electrons from its partner for the formation of new covalent bond. Thereinto, coupling reactions could be categorized as redox‐neutral cross‐coupling with an electrophile and a nucleophile, oxidative coupling with two nucleophiles, and reductive coupling with two electrophiles (Scheme 1.1).
Scheme 1.1 Cross‐coupling reactions with nucleophiles and electrophiles.
In organic chemistry, the nucleophile is an electron‐rich molecule that contains a lone pair of electrons or a polarized bond, the heterolysis of which also could yield a lone pair of electrons (Scheme 1.2). According to this concept, organometallic compounds, alcohols, halides, amines, and phosphines with a lone pair of electrons are nucleophiles. Some nonpolar π bonds, including olefins and acetylenes, which could donate the π‐bonding electrons, are often considered to be nucleophiles. Moreover, the C—H bonds of hydrocarbons can be considered to be nucleophiles because the electronegativity of carbon is higher than that of hydrogen, which could deliver a proton to form a formal carbon anion. Correspondingly, the electrophile is an electron‐deficient molecule that contains unoccupied orbitals or low‐energy antibonding molecular orbital, which could accept the electrons from nucleophiles. In this chemistry, cationic carbons, which usually come from the heterolysis of carbon—halogen bonds, are electrophile. Polar π bonds, including carbonyl compounds and imines, also could be considered to be electrophile, which involve a low‐energy π antibond. Interestingly, Fisher‐type singlet carbene has an electron pair filling one sp2 hybrid orbital and an unoccupied p orbital, which could be considered to be either nucleophile or electrophile in coupling reactions.
