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A Cobalt(I) Pincer Complex with an η2‐Caryl−H Agostic Bond: Facile C−H Bond Cleavage through Deprotonation,Radical Abstraction,and Oxidative Addition
Authors:Sathiyamoorthy Murugesan  Dr. Berthold Stöger  Dr. Ernst Pittenauer  Prof. Dr. Günter Allmaier  Prof. Dr. Luis F. Veiros  Prof. Dr. Karl Kirchner
Affiliation:1. Institute of Applied Synthetic Chemistry, Vienna University of Technology, Wien, Austria;2. Institute of Chemical Technologies and Analytics, Vienna University of Technology, Wien, Austria;3. Centro de Química Estrutural, Instituto Superior Técnico, Universidade de Lisboa, Lisboa, Portugal;4. http://www.ias.tuwien.ac.at
Abstract:The synthesis and reactivity of a CoI pincer complex [Co(?3P,CH,P‐P(CH)PNMeiPr)(CO)2]+ featuring an η2‐ Caryl?H agostic bond is described. This complex was obtained by protonation of the CoI complex [Co(PCPNMeiPr)(CO)2]. The CoIII hydride complex [Co(PCPNMeiPr)(CNtBu)2(H)]+ was obtained upon protonation of [Co(PCPNMeiPr)(CNtBu)2]. Three ways to cleave the agostic C?H bond are presented. First, owing to the acidity of the agostic proton, treatment with pyridine results in facile deprotonation (C?H bond cleavage) and reformation of [Co(PCPNMeiPr)(CO)2]. Second, C?H bond cleavage is achieved upon exposure of [Co(?3P,CH,P‐P(CH)PNMeiPr)(CO)2]+ to oxygen or TEMPO to yield the paramagnetic CoII PCP complex [Co(PCPNMeiPr)(CO)2]+. Finally, replacement of one CO ligand in [Co(?3P,CH,P‐P(CH)PNMeiPr)(CO)2]+ by CNtBu promotes the rapid oxidative addition of the agostic η2‐Caryl?H bond to give two isomeric hydride complexes of the type [Co(PCPNMeiPr)(CNtBu)(CO)(H)]+.
Keywords:agostic interactions  C−  H activation  cobalt  pincer complexes  protonation
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