{"title":"Moving from Fuel to Feedstock: Selective Hydrocarbon Activation using Rhodium and Iridium Complexes","authors":"Paul A. Morton, S. M. Mansell","doi":"10.1595/205651323x16765646706676","DOIUrl":null,"url":null,"abstract":"Carbon-hydrogen bond activations and their subsequent functionalisation have long been an important target in chemistry because C-H bonds are ubiquitous throughout nature, making C-H derivatisation reactions highly desirable. The selective and efficient functionalisation of this bond into many more useful carbon-element bonds (e.g., C-B, C-Si, C-O, and C-S bonds) would have many uses in pharmaceutical and bulk chemical synthesis. Activation of the C-H bond is, however, challenging due to the high strength and low bond-polarity of this bond rendering its cleavage unfavourable. With the correct choice of reagents and systems, especially those utilising directing groups, kinetically and thermodynamically favourable catalytic processes have been developed. However, a key remaining challenge is the development of undirected, intermolecular reactions using catalysts that are both selective and active enough to make useful processes. In this review, the progress towards optimising group 9 C-H activation catalysts is discussed, particularly focusing on undirected reactions that are kinetically more difficult, starting with a brief history of C-H activation, identifying the importance of auxiliary ligands including the nature of anionic ligand (e.g., cyclopentadienyl, indenyl, fluorenyl, trispyrazolylborate) and neutral ligands (e.g., phosphines, carbonyl, alkenes, N-heterocyclic carbenes) that contribute towards the stability and reactivity of these metal complexes. The tethering of the anionic ligand to strong σ-donating ligands is also briefly discussed. The focus of this review is primarily on the group 9 metals rhodium and iridium, however, C-H activation using group 8 and 10 metals are compared where useful. The most recent advances in this field include the development of C-H borylation of many small hydrocarbon substrates such as arenes, heterocycles and n-alkanes as well as the more challenging substrate methane.","PeriodicalId":14807,"journal":{"name":"Johnson Matthey Technology Review","volume":"1 1","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Johnson Matthey Technology Review","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1595/205651323x16765646706676","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Carbon-hydrogen bond activations and their subsequent functionalisation have long been an important target in chemistry because C-H bonds are ubiquitous throughout nature, making C-H derivatisation reactions highly desirable. The selective and efficient functionalisation of this bond into many more useful carbon-element bonds (e.g., C-B, C-Si, C-O, and C-S bonds) would have many uses in pharmaceutical and bulk chemical synthesis. Activation of the C-H bond is, however, challenging due to the high strength and low bond-polarity of this bond rendering its cleavage unfavourable. With the correct choice of reagents and systems, especially those utilising directing groups, kinetically and thermodynamically favourable catalytic processes have been developed. However, a key remaining challenge is the development of undirected, intermolecular reactions using catalysts that are both selective and active enough to make useful processes. In this review, the progress towards optimising group 9 C-H activation catalysts is discussed, particularly focusing on undirected reactions that are kinetically more difficult, starting with a brief history of C-H activation, identifying the importance of auxiliary ligands including the nature of anionic ligand (e.g., cyclopentadienyl, indenyl, fluorenyl, trispyrazolylborate) and neutral ligands (e.g., phosphines, carbonyl, alkenes, N-heterocyclic carbenes) that contribute towards the stability and reactivity of these metal complexes. The tethering of the anionic ligand to strong σ-donating ligands is also briefly discussed. The focus of this review is primarily on the group 9 metals rhodium and iridium, however, C-H activation using group 8 and 10 metals are compared where useful. The most recent advances in this field include the development of C-H borylation of many small hydrocarbon substrates such as arenes, heterocycles and n-alkanes as well as the more challenging substrate methane.
期刊介绍:
Johnson Matthey Technology Review publishes articles, reviews and short reports on science enabling cleaner air, good health and efficient use of natural resources. Areas of application and fundamental science will be considered in the fields of:Advanced materials[...]Catalysis[...][...]Characterisation[...]Electrochemistry[...]Emissions control[...]Fine and speciality chemicals[...]Historical[...]Industrial processes[...]Materials and metallurgy[...]Modelling[...]PGM and specialist metallurgy[...]Pharmaceutical and medical science[...]Surface chemistry and coatings[...]Sustainable technologies.