Abstract
Kinetic study of organic reactions, especially
multistep catalytic reactions, is crucial to in-depth understanding of reaction
mechanisms. Here we report our kinetic study of the chiral disulfonimide
catalyzed cyanosilylation of aldehyde, which reveals that two molecules of
TMSCN are involved in the rate-determining C-C bond forming step. In addition,
the apparent activation energy, enthalpy of activation and entropy of
activation were deduced through the study of temperature dependence of the
reaction rates. More importantly, a novel and efficient method which makes use
of the progress rates was developed to treat the kinetic data obtained from continuous monitoring of the reaction progress with in situ FT-IR.
Supplementary materials
Title
Kinetic Study - SI 20200405
Description
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