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Synthesis of organopalladium(IV) complexes by halogen exchange,and the structure of the azidopalladium(II) complex formed on reductive elimination of ethane from Pd(N)3Me2(CH2Ph)(bpy)
Institution:1. Department of Chemistry, Texas A&M University, College Station, TX 77843-3255, USA;1. State Key Laboratory of Pollution Control and Resources Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092, China;2. Shanghai Institute of Pollution Control and Ecological Security, Shanghai 200092, China;1. State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian National Laboratory for Clean Energy, Liaoning Province, Dalian 116023, China.;2. Carbon Research Laboratory, Liaoning Key Lab for Energy Materials and Chemical Engineering, State Key Lab of Fine Chemicals, Dalian University of Technology, Dalian 116024, China.;1. Department of Mechanical Engineering, University of New Orleans, United States;2. Advanced Materials Research Institute (AMRI), University of New Orleans, United States;1. School of Chemistry, Joseph Black Building, David Brewster Road, Edinburgh, EH9 3FJ, United Kingdom;2. Evotec (UK) Ltd, 114 Innovation Drive, Milton Park, Abingdon, Oxfordshire OX14 4RZ, United Kingdom
Abstract:A new route to organopalladium(IV) complexes is described, involving replacement of bromine in the 2,2′-bipyridyl complex PdBrMe2(CH2Ph)(by), by other halogen or pseudohalogen groups. 1H NMR studies of the decomposition of PDXMe2(CH2Ph)(bpy) in warm (CD3)2CO indicate that a selectivity in reductive elimination of alkanes occurs. to give ethane (X = Br, N3, NCS), or a mixture of ethane and ethylbenzene in ca. 9/1 ratio (X = F. Cl, I). The reductive elimination product azido(2,2′-bipyridyl)benzylpalladium(II) has been characterized by X-ray crystallography.
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