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Theoretical Studies of Inorganic and Organometallic Reaction Mechanisms. 15. Catalytic Alkane Dehydrogenation by Iridium(III) Complexes
Alkane dehydrogenation catalyzed by the Ir(III) complexes (PCP‘)Ir(H)2 (1) [PCP‘ = η3-C6H3(CH2PH2)2-1,3] and CpIr(PH3)(H)+ (10) [Cp = η5-C5H5] is investigated with density functional theory (DFT). For both systems the theoretical results show that catalytic alkane dehydrogenation to alkene proceeds...
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Published in: | Journal of the American Chemical Society 1999-04, Vol.121 (16), p.3992-3999 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Alkane dehydrogenation catalyzed by the Ir(III) complexes (PCP‘)Ir(H)2 (1) [PCP‘ = η3-C6H3(CH2PH2)2-1,3] and CpIr(PH3)(H)+ (10) [Cp = η5-C5H5] is investigated with density functional theory (DFT). For both systems the theoretical results show that catalytic alkane dehydrogenation to alkene proceeds through (i) alkane oxidative addition, (ii) dihydride reductive elimination, (iii) β-H transfer from alkyl ligand to metal, and finally (iv) elimination of the olefin. Barriers for steps (i), (ii), and (iv) are critical for the catalytic cycle. The (PCP‘)Ir(H)2 system is special because these three barriers are balanced (16, 15, and 22 kcal/mol, respectively), whereas in the CpIr(PH3)(H)+ system these three barriers are unbalanced (9, 24, and 41 kcal/mol, respectively). Thus, in the catalytic cycle for alkane dehydrogenation by (PCP‘)Ir(H)2 the reaction endothermicity is achieved gradually. The higher stability of the formally Ir(V) complexes and the η2-alkene complex, which has some Ir(V)-like character, in the CpIr(PH3)(H)+ system is responsible for the larger barriers in these critical steps. In the key role played by the ligand systems, PCP‘(H) vs Cp(PH3), the former increases the energy of the metal−ligand fragment's triplet state relative to that of the singlet and thus destabilizes all the Ir(V)-like species. |
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ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/ja981314d |