Journal
JOURNAL OF ORGANOMETALLIC CHEMISTRY
Volume 691, Issue 21, Pages 4434-4445Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2006.03.004
Keywords
ruthenium; cobalt; rhodium; alkynes; nitriles; cycloaddition; pyridine formation; DFT calculations
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The mechanism of the catalytic formation of pyridines from the coupling of two alkynes and the nitriles N CR (R = H, Me, Cl, COOMe) with the fragments CpRuCl, CpCo, and CpRh has been investigated by means of DFT/B3LYP calculations. According to the proposed mechanism, the key reaction step is the oxidative coupling of two alkyne ligands to give metallacyclopentatriene (Ru, Rh) and metallacyclopentadiene (Co) intermediates. In the case of ruthenium, this process is thermodynamically clearly favored over the oxidative coupling between one alkyne and one nitrile ligand to afford an azametallacycle. This alternative pathway however cannot be dismissed in the case of Co and Rh. The rate determining step of the overall catalytic cycle is the addition of a nitrile molecule to the metallacyclopentatriene and metallacyclopentadiene intermediates, respectively, which has to take place in a side-on fashion. Competitive alkyne addition leads to benzene formation. Thus, also the chemo selectivity of this reaction is determined at this stage of the catalytic cycle. In the case of the RuCpCl fragment, the addition of nitriles R-C N and acetylenes RC CH has been studied in more detail. For R = H, Cl, and COOMe the side-on addition of nitriles is kinetically more favored than alkyne addition and, in accordance with experimental results, pyridine formation takes place. In the case of R = Me nitrile addition could not be achieved and the addition of alkynes to give benzene derivatives seems to be kinetically more favored. Once the nitrile is coordinated facile C-C bond coupling takes place to afford an unusual five- and four-membered bicyclic ring system. This intermediate eventually rearranges to a very unsymmetrical azametallaheptatriene complex which in turn provides CpRuCl(kappa(1)-pyridine) via a reductive elimination step. Completion of the catalytic cycle is achieved by an exergonic displacement of the respective pyridine product by two acetylene molecules regenerating the bisacetylene complex. (c) 2006 Elsevier B.V. All rights reserved.
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