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作 者:唐诗雅[1] 于海珠[1] 尤万里[1] 郭庆祥[1]
出 处:《Chinese Journal of Chemical Physics》2013年第4期415-423,J0001,共10页化学物理学报(英文)
摘 要:Pd-catalyzed oxidative C-H/C-H coupling reaction is an emerging type of C-H acti- vation reaction, which attracts great interests because both reaction partners do not re- quire pre-functionalization. In the present study, we employed DFT methods to investigate the mechanism of Pd(OAc)2-catalyzed oxidative C-H/C-H coupling of pentafluoroben-zene with benzene. Four possible pathways were examined in the C-H activation part: path A benzene-pentafluorobenzene mechanism (C-H activation of benzene occurs before the C-H activation of pentafluorobenzene), path B pentafluorobenzene-benzene mechanism (C-H activation of benzene occurs after the C-H activation of pentafluorobenzene), path C benzene-pentafluorophenylsilver mechanism (C-H activation of benzene and subsequent transmetalation with pentafiuorophenyl silver complex), path D pentafiuorophenylsilver- benzene mechanism (transmetalation with pentafluorophenyl silver complex and subsequent C-H activation of benzene). Based on the calculations, the sequences of two C-H activation steps are found to be different in the oxidative couplings of same substrates (i. e. pentafiu- orobenzene and benzene) in different catalytic systems, where the additive Ag salts played a determinant role. In the absence of Ag salts, the energetically favored pathway is path B (i.e. the C-H activation of pentafluorobenzene takes place before the C-H cleavage of benzene). In contrast, with the aid of Ag salts, the coordination of pentafluorophenylsilver to Pd center could occur easily with a subsequent C-H activation of benzene in the second step, and the second step significantly raises the whole reaction barrier. Alternatively, in the presence of Ag salts, the kinetically preferred mechanism is path C (i. e. the C-H activation of benzene takes place in the first step followed by transmetalation with pentafluorophenyl- silver complex), which is similar to path A. The calculations are consistent with the H/D exchange experiment and kinetic isotope effects. Thus
关 键 词:Pd catalysis Oxidative coupling C-H activation Mechanism Pentafluo-robenzene
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