An Uncanny Dehydrogenation Mechanism: Polar Bond Control over Stepwise or Concerted Transition States

作者：Bellows Sarina M; Chakraborty Sumit; Gary J Brannon; Jones William D; Cundari Thomas R

来源：Inorganic Chemistry, 2017, 56(10): 5519-5524.

DOI：10.1021/acs.inorgchem.6b01800

The mechanism of the dehydrogenation of N-heterocycles with the recently established bifunctional catalyst ((PNP)-P-iPr)Fe(CO)(H) was investigated through experiments and density functional theory calculations ((PNP)-P-iPr = (i)Pr(2)PCH(2)CH(2)NCH(2)CH(2)PiPr(2)). In this system, the saturated N-heterocyclic substrates are completely dehydrogenated to the aromatic products. Calculations indicate that dehydrogenation barriers of the C-C bonds are very high in energy (Delta G = 37.4-42.2 kcal/mol), and thus dehydrogenation only occurs at the C-N bond (Delta G = 9.622.2 kcal/mol). Interestingly, substrates like piperidine with relatively unpolarized C-N bonds are dehydrogenated through a concerted proton/hydride transfer bifunctional transition state involving the nitrogen on the PNP ligand. However, substrates with polarized C-N bonds entail stepwise (proton then hydride) bifunctional dehydrogenation.

• 出版日期2017-5-15