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[null,"1.","Record Nr.",null,"UNINA9910418316603321"]
[null,null,"Autore",null,"Knoll Daniel"]
[null,null,"Titolo",null,"Heterobimetallic [2.2]paracyclophane complexes and their application in photoredox catalysis / / Daniel Knoll"]
[null,null,"Pubbl/distr/stampa",null,"Berlin/Germany, : Logos Verlag Berlin, 2020"]
[{"$nulls":4},"Berlin, Germany : , : Logos Verlag Berlin GmbH, , [2020]"]
[{"$nulls":4},"©2020"]
[null,null,"ISBN",null,"9783832550714"]
[null,null,"Descrizione fisica",null,"1 online resource (xiii, 212 pages) : illustrations; digital file(s)"]
[null,null,"Collana",null,"Beiträge zur organischen Synthese ; 85"]
[null,null,"Soggetti",null,"Heterobimetallic complexes"]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Author's doctoral thesis, Karlsruher Institut für Technologie (KIT) -- title-page recto."]
[null,null,null,"Nota di bibliografia","Includes bibliographical references."]
[null,null,null,"Sommario/riassunto","The most important goal of current chemistry research is to provide green and sustainable routes to compounds of interest. One way of addressing this is the use of abundant and inexpensive sources of energy to drive reactions, with the prime example being visible light in photoredox catalysis. One recent promising approach is the use of heterobimetallic catalysts where two metals work in a cooperative fashion to achieve the desired transformation. However, these cooperative effects are poorly understood due to a lack of model complexes suitable for the intricate study of heterobimetallic complexes. In this work, [2.2]paracyclophane (PCP) is presented as a new platform on which to build distance-variable heterobimetallic complexes. The methods for the access to these synthetic targets are developed and investigated for their broader synthetic applicability. To demonstrate the potential of these complexes as catalysts, Au/Ru heterobimetallic complexes are evaluated regarding their performance in a dual photoredox catalytic arylative Meyer-Schuster rearrangement reaction. This reaction provides a very convenient and sustainable access Î±-arylated enones, an important building blocks for relevant pharmaceutical compounds."]