An Electronic Structure Study of the Conversion from 1,2-Diphenylacetylene to (E)-1,2-Diphenylethene Using a Bidentate Ru(II)-NC Catalyst

Full text
Author(s):	Curichimba, Jeyson Esquivel ; Andrade Haiduke, Roberto Luiz Total Authors: 2
Document type:	Journal article
Source:	European Journal of Inorganic Chemistry; v. N/A, p. 10-pg., 2022-10-25.
Abstract
The {(C5H4N)(C6H4)}RuCl(CO)(PPh3)(2) catalyst has been shown to be highly efficient and selective for semi-hydrogenation reactions with a wide range of internal alkynes containing electron-withdrawing and electron-donating groups to E-alkenes. In this work, the reaction mechanism previously proposed by experimentalists to the formation of (E)-1,2-diphenylethene from 1,2-diphenylacetylene (Organometallics, 2020, 39, 862) is evaluated by using the Density Functional Theory. Our calculations show the existence of four new intermediates to avoid steric hindrance issues and to explain the releasing of the (Z)-1,2-diphenylethene and (E)-1,2-diphenylethene products at the end of the first and second cycles, respectively. Besides, by using the energetic span model, the turnover frequency (TOF)-determining transition state (TDTS) and intermediate (TDI) are found in the first cycle, providing an energetic span for the catalytic cycle of 16.8 kcal/mol at 383.15 K. This result assures that the reaction can really proceed by this mechanism. (AU)

FAPESP's process:	14/23714-1 - Electronic structure relativistic calculations for evaluation of new prolapse-free basis sets
Grantee:	Roberto Luiz Andrade Haiduke
Support Opportunities:	Regular Research Grants