Premium
DFT Study on Dinuclear Palladium Complex Catalyzed Pyrrole Formation From tert ‐Butyl Isocyanide and Alkynes
Author(s) -
Lai Xiaoling,
Li Yang
Publication year - 2021
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.202100142
Subject(s) - isocyanide , chemistry , palladium , regioselectivity , isomerization , catalysis , migratory insertion , catalytic cycle , alkyne , intramolecular force , substituent , photochemistry , ligand (biochemistry) , medicinal chemistry , combinatorial chemistry , stereochemistry , organic chemistry , biochemistry , receptor
Density functional theory calculations were carried out to study the mechanisms of Pd‐catalyzed reactions of alkynes with tert ‐butyl isocyanide forming pyrroles. In the case of di ‐palladium catalysis, the calculations indicated that alkyne insertion, isocyanide insertion, intramolecular cyclization, isocyanide insertion, isomerization and ligand substitution were involved in the mechanism. The intramolecular cyclization process was calculated to be the rate‐determining step in the catalytic cycle. The substituent effects on the regioselectivity of reaction were also analyzed. In addition, detailed calculations on mono‐palladium catalysis showed that the activity of mononuclear catalysis was not as high as that of di ‐palladium catalysis. These calculation results were in good agreement with the experimental results.