Theoretical study on selectivity trends in (N-heterocyclic carbene)-Pd catalyzed mizoroki-heck reactions: Exploring density functionals methods and molecular models
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Data
2017-10-30
Autores
Menezes da Silva, Vitor H. [UNESP]
Lima Batista, Ana Paula de [UNESP]
Navarro, Oscar
Braga, Ataualpa A. C. [UNESP]
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Wiley-Blackwell
Resumo
The regioselectivity of the NHC-Pd catalyzed Heck coupling reaction between phenyl bromide and styrene has been investigated using the density functional theory, wave-function (WF)-based methods and two different sizes of model ligands. In addition to the WF methods, the TPSS-D3, B97X-D, BP86-D3, and M06-L density functionals were reliable approaches to be applied, independently of the basis set. Moreover, the NCI analysis showed that weak interactions are important forces to be taken into account when exploring the regioselectivity of this reaction, mainly when a crowded NHC ligand is present. (c) 2017 Wiley Periodicals, Inc.
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N-heterocyclic carbene ligands, Heck reactions, selectivity, non-covalent interactions, DFT methods
Como citar
Journal Of Computational Chemistry. Hoboken: Wiley, v. 38, n. 28, p. 2371-2377, 2017.