# Self-Thickening Materials Derived from Phenylpropanoid Ene Reactions

## TL;DR

This paper explores chemical reactions between phenylpropanoid compounds and DEAD, resulting in self-thickening materials that could be used as thickening agents in solvents.

## Contribution

The study identifies uncatalyzed ene reactions and self-thickening properties in phenylpropanoid-derived materials.

## Key findings

- Phenylpropanoid compounds react with DEAD to form ene products and complex byproducts.
- Products exhibit self-thickening behavior in their pure form but lose viscosity when diluted.
- NMR and FTIR analyses confirmed the structures and reaction mechanisms.

## Abstract

In this work, we report the observation of uncatalyzed ene reactions between several phenylpropanoid compounds and diethyl azodicarboxylate (DEAD). For allylbenzene, the reaction produces the ene product at molar ratios of up to 1:2 of allylbenzene to DEAD. At higher levels of DEAD, more complex reactions are observed. For the reaction between methyl eugenol and DEAD, similar ene reaction products have been found. However, the reaction of eugenol with DEAD is more complex; in addition to the ene reaction, other reactions happen at the same time. Most of the structures of the resulting products have been elucidated using NMR spectroscopy (1H, 13C, and 2D), and the findings have been further corroborated by FTIR analysis. Interestingly, these products appear to undergo molecular aggregation, which results in self-thickening in their neat form. However, the viscosity significantly decreases upon dilution with a solvent. This self-thickening property suggests their potential use as thickening agents in organic solvent formulations.