04186nam 22006735 450 991029863420332120200704024928.03-319-18690-610.1007/978-3-319-18690-0(CKB)3710000000434148(EBL)2120635(OCoLC)916951321(SSID)ssj0001525278(PQKBManifestationID)11936252(PQKBTitleCode)TC0001525278(PQKBWorkID)11485264(PQKB)11430967(DE-He213)978-3-319-18690-0(MiAaPQ)EBC2120635(PPN)186401388(EXLCZ)99371000000043414820150613d2015 u| 0engur|n|---|||||txtccrSynthesis and Original Reactivity of Copper and Gold Complexes[electronic resource] σ-Bond Coordination, Oxidative Addition, Migratory Insertion /by Maximilian Joost1st ed. 2015.Cham :Springer International Publishing :Imprint: Springer,2015.1 online resource (244 p.)Springer Theses, Recognizing Outstanding Ph.D. Research,2190-5053Description based upon print version of record.3-319-18689-2 Includes bibliographical references.General Introduction -- Copper: σ-SiH Coordination to Cu(I) -- Fundamental Elementary Steps in Gold Chemistry -- Gold: Migratory Insertion at Au(I) -- Gold: Oxidative Addition to Au(I) -- General Conclusion and Perspective -- Appendix: Crystallographic Data.This thesis addresses the coordination chemistry and reactivity of copper and gold complexes with a focus on the elucidation of (i) the metal-mediated activation of σ-bonds and (ii) the migratory insertion reaction. Both processes are of considerable importance in organometallic chemistry, but remain elusive for Cu and Au complexes. In this work, the author contributes significant advances: The first σ-SiH complexes of copper are experimentally and computationally characterized, yielding valuable insights into σ-bond activation processes for copper. Evidence for a highly unusual migratory syn insertion of unsaturated organic molecules into the gold-silicon bond of silylgold (I) complexes is provided and the corresponding mechanism identified. The intermolecular oxidative addition of σ-SiSi, σ-CC and σ-CX (X=halogen) bonds with molecular gold (I) complexes is studied in detail, effectively demonstrating that this reaction, usually considered to be impossible for gold, is actually highly favored, provided an adequate ligand is employed. The use of small-bite angle bis (phosphine) gold (I) complexes allows for the first time the oxidative addition of σ-CC and σ-CX bonds for gold (I). These results shed light on an unexpected reactivity pattern of gold complexes and may point the way to 2-electron redox transformations mediated by this metal, opening up new perspectives in gold catalysis.Springer Theses, Recognizing Outstanding Ph.D. Research,2190-5053Organometallic chemistry Physical chemistryChemoinformaticsOrganometallic Chemistryhttps://scigraph.springernature.com/ontologies/product-market-codes/C19020Physical Chemistryhttps://scigraph.springernature.com/ontologies/product-market-codes/C21001Computer Applications in Chemistryhttps://scigraph.springernature.com/ontologies/product-market-codes/C13009Organometallic chemistry .Physical chemistry.Chemoinformatics.Organometallic Chemistry.Physical Chemistry.Computer Applications in Chemistry.54541541.0285547.05Joost Maximilianauthttp://id.loc.gov/vocabulary/relators/aut974047BOOK9910298634203321Synthesis and Original Reactivity of Copper and Gold Complexes2217269UNINA