Theoretical study of asymmetric transfer hydrogenation of ketones catalyzed by amino acid derived rhodium complexes

Nordin, MikaelStockholms universitet,Institutionen för organisk kemi (författare)

AuthorCount:5;
Density functional theory calculations are employed to study the asymmetric transfer hydrogenation of ketones catalyzed by rhodiumarene complexes containing hydroxamic acid-functionalized amino acid ligands. Firstly, the ligandmetal binding is investigated and it is shown that both the N,N and O,O binding modes Are viable. For each of these, the full free energy profile for the transfer hydrogenation is calculated according to the outer-sphere reaction mechanism. Three factors are demonstrated to influence the stereoselectivity of the process, namely the energy difference between the metalligand binding modes, the energy difference between the intermediate hydrogenated catalyst, and the existence of a stabilizing CHp interaction between the Cp* ligand of the catalyst and the phenyl moiety of the substrate. Theoretical reproduction of the selectivity of a slightly modified ligand that is shown experimentally to yield the opposite enantioselectivity corroborates these results. Finally, a technical observation made is that inclusion of dispersion interactions (using the B3LYP-D2 correction or the M06 functional) proved to be very important for reproducing the enantioselectivity.

Liao, Rong-Zhen (författare)
Ahlford, KatrinStockholms universitet,Institutionen för organisk kemi (författare)
Adolfsson, HansStockholms universitet,Institutionen för organisk kemi(Swepub:su)hansa (författare)
Himo, FahmiStockholms universitet,Institutionen för organisk kemi(Swepub:su)himo (författare)
Stockholms universitetInstitutionen för organisk kemi (creator_code:org_t)

Av författaren/redakt...: Nordin, Mikael; Liao, Rong-Zhen; Ahlford, Katrin; Adolfsson, Hans; Himo, Fahmi

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