Kinetics and mechanism of the reaction between 2,3,4,5,6-pentafluorophenylacetonitrile and guanidine-like bases and the structure of the products

doi:10.1016/J.MOLSTRUC.2006.02.015

Paper

Kinetics and mechanism of the reaction between 2,3,4,5,6-pentafluorophenylacetonitrile and guanidine-like bases and the structure of the products

Published Aug 7, 2006 · B. Gierczyk, G. Schroeder, P. Przybylski

Journal of Molecular Structure

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4

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Abstract

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Study Snapshot

The reaction between 2,3,4,5,6-pentafluorophenylacetonitrile and guanidine-like bases produces ortho or para substituted dimers and a mixture of trimers, tetramers, and pentamers of PFPA in a relatively slow process.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Kinetics and mechanism of the reaction between 2,3,4,5,6-pentafluorophenylacetonitrile and guanidine-like bases and the structure of the products

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