Related Experiment Video
Updated: Jun 24, 2026

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
Trans-cinnamic acid and coumarin-3-carboxylic acid: experimental charge-density studies to shed light on [2 + 2]
Judith A K Howard1, Mary F Mahon, Paul R Raithby
1Department of Chemistry, University Science Laboratories, Durham University, South Road, Durham DH1 3LE, England.
Abstract:
As part of an ongoing series of experimental charge-density investigations into the intra- and intermolecular interactions present in compounds which undergo solid-state [2 + 2] cycloaddition reactions, the charge-density analyses of trans-cinnamic acid and coumarin-3-carboxylic acid are reported. Thus, high-resolution single-crystal X-ray diffraction data were recorded at 100 K for trans-cinnamic acid (sin theta/lambda(max) = 1.03 A(-1)) and coumarin-3-carboxylic acid (sin theta/lambda(max) = 1.19 A(-1)). In addition to the anticipated O-H...O hydrogen bonds weak C-H...O interactions were identified in both structures along with very weak intermolecular interactions between pairs of molecules that undergo solid-state [2 + 2] cycloaddition reactions upon irradiation.
Related Concept Videos
Cycloaddition Reactions: Overview
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group with both...
Cycloaddition Reactions: MO Requirements for Thermal Activation
Cycloaddition Reactions: MO Requirements for Photochemical Activation
Aromatic Hydrocarbon Anions: Structural Overview
Due to the absence of continuous overlap of p...
Disubstituted Cyclohexanes: cis-trans Isomerism
In cyclohexane, the substituents can occupy different positions generating distinct isomers.

