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dc.contributor.authorCao, ZX
dc.contributor.author曹泽星
dc.contributor.authorHall, MB
dc.date.accessioned2012-06-18T01:15:54Z
dc.date.available2012-06-18T01:15:54Z
dc.date.issued2000-07-22
dc.identifier.citationOrganometallics, 2000, 19 (17), pp 3338–3346zh_CN
dc.identifier.issn0276-7333
dc.identifier.urihttp://dx.doi.org/doi:10.1021/om991015c
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/12827
dc.description.abstractActivation of C-C and C-H bonds by the Rh(I) and Ir(I) complexes (PCB)MCl (M = Rh, Ir; PCP = C6H3(CH3)(CH2PH2)(2)) has been studied by density functional methodology. C-H activation from either of the three-coordinate intermediates la and Ib has a high barrier (>25 kcal/mol). Direct C-C activation does not occur from either la or Ib because the C-C bond is sterically inaccessible. Plausible C-C and C-H activation mechanisms under mild conditions are related to four-coordinate eta(1)-arene intermediates, 3a or 3b, which are formed prior to the activation processes. Activation energies for the direct C-C oxidative addition at Rh(I) and Ir(I) were calculated to be 14.3 and 12.6 kcal/mol, respectively. The C-C bond activation products form with an exothermicity of -4.4 and -24.1 kcal/mol relative to the eta(1)-arene intermediates 3a and 3b, respectively. The unexpected reactivity for C-C activation in PCP ligand systems can be ascribed to the formation of the eta(1)-arene intermediates and the existence of strong Ar-metal bonds in transition states for C-C bond activation. The former makes the C-C bond accessible to the metal center, and the latter significantly reduces the barrier of the C-C activation process. "Solvent" coordination also stabilizes the C-C activation product more than the C-H activation product.zh_CN
dc.language.isoenzh_CN
dc.publisherAMER CHEMICAL SOCzh_CN
dc.titleTheoretical studies of inorganic and organometallic reaction mechanisms. 17. Unprecedented C-C bond activation at rhodium(I) and iridium(I)zh_CN
dc.typeArticlezh_CN


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