Related Experiment Video
Updated: Feb 10, 2026

Covalent Binding of BMP-2 on Surfaces Using a Self-assembled Monolayer Approach
Published on: August 26, 2013
Wavelength-resolved heterodimer [2 + 2] photocycloadditions for reversible surface grafting
Dushani Kanchana1, Lauren Geurds1, Aaron Micallef2
1School of Chemistry and Physics, Centre for Materials Science, Queensland University of Technology (QUT) 2 George Street Brisbane QLD 4000 Australia k.mundsinger@qut.edu.au christopher.barnerkowollik@qut.edu.au.
None:
We report the first wavelength-dependent quantum yields of a [2 + 2] photocycloaddition generating the heterodimers of 7-hydroxycoumarin (7HCou) and styrene via a photochemical action plot. The wavelength-dependent heterodimer quantum yields are quantified at a constant number of photons at each wavelength between 310 and 370 nm. The resulting wavelength-dependent quantum yields demonstrate that the heterodimer is most efficiently generated at 345 nm, red-shifted by close to 25 nm compared to the absorption maximum of 7HCou at 320 nm. We subsequently translate these findings to photochemical surface functionalization by exploiting heterodimer formation between a surface bound coumarin derivative and para-styrene perfluoroalkyl ether (StyPFA) on surfaces under 345 nm irradiation to reversibly modulate surface hydrophobicity. The reversibility of the surface heterodimerization is demonstrated by removing StyPFA under UVC irradiation, and re-functionalization on the same surface. Functional heterodimer formation and the reversibility of the reaction on surface are followed via surface-sensitive X-ray photoelectron spectroscopy (XPS) and contact angle measurements. We subsequently apply our photochemical surface functionalization strategy to a dual cure photoresin based on a polyurethane-acrylate interpenetrating network, without deterioration of its mechanical properties, thereby confirming the feasibility of a photocycloaddition-based functionalization strategy for photoresins.
Related Concept Videos
meta-Directing Deactivators: –NO2, –CN, –CHO, –⁠CO2R, –COR, –CO2H
2° Amines to N-Nitrosamines: Reaction with NaNO2
The de Broglie Wavelength
SN2 Reaction: Kinetics
In a chemical reaction, a relationship exists between the concentration of reactants and the rate at which the reaction proceeds. The study to measure this relationship is known as the kinetics of a chemical reaction. Kinetic studies are used to deduce the rate law of a chemical reaction, which provides information about the species involved during the transition state of the rate-determining step. Thus, kinetic studies help to derive the mechanism of a...
SN2 Reaction: Mechanism
The presence of the more electronegative halogen in the substrate creates a polarized carbon-halide bond. The halide pulls the electron cloud generating an electrophilic center at the carbon atom. Thus, the carbon atom carries a partial positive charge while the halide has a...
SN2 Reaction: Transition State
When the nucleophile approaches the electrophilic carbon with its lone pairs, the halide acts as a leaving group and moves away with the electron-pair bonded to the carbon. Dotted partial bonds represent the bonds being formed or broken...

