Journal
CHEMISTRY-A EUROPEAN JOURNAL
Volume 19, Issue 3, Pages 1020-1027Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201202185
Keywords
density functional calculations; hydroamination; iridium; oxidative addition; pincer ligands; rhodium
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Funding
- DFG (International Research Training Group 1628 Selectivity in Chemo- and Biocatalysis)
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Very few cases of oxidative addition of NH3 to transition-metal complexes forming terminal amide hydrides have been experimentally observed. Here, two examples with the iridium pincer complexes [Ir(PCP)(NH3)] A1 with PCP=[?3-(tBu2P-C2H4)2CH]- and [Ir(PSiP)(NH3)] B1 with PSiP=[?3-(2-Cy2P-C6H4)2SiMe]- were investigated by DFT calculations applying the M06L density functional to successfully reproduce the trend of the experimentally observed thermochemical stabilities. According to the calculations, the corresponding hydrido-amido complexes A2 and B2 are more stable than the corresponding ammine complexes by ?G=-2.8 and -2.6 kcal?mol-1, respectively. Complexes such as A2 and B2 are ideally suited entry points to catalytic cycles for the hydroamination of ethylene with ammonia. Therefore, the relevant stationary points of the potentially available cycles were studied computationally to verify if these complexes can catalyze the hydroamination. As a result, complex A2 will clearly not catalyze the hydroamination as all energy spans calculated range close to 40 kcal?mol-1 or higher. The energy spans obtained with B2 are significantly lower in some cases and range around 35 kcal?mol-1, further indicating that no turnover can be expected. By systematically varying the structure of B2, the energy span could be reduced to 28.8 kcal?mol-1 corresponding to a TOF of 17 h-1 at a reaction temperature of 140?degrees C. A reoptimization of relevant structures under the inclusion of cyclohexane as a typical solvent reduces the calculated TOF to 6.0 h-1.
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