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Published on: October 9, 2012
Photochemically driven shape changes of crystalline organic nanorods
Rabih O Al-Kaysi1, Astrid M Müller, Christopher J Bardeen
1Department of Chemistry, University of California, Riverside, California 92521, USA.
Journal of the American Chemical Society
|December 15, 2006
Summary
Organic nanorods of 9-tert-butylanthroate (9-TBAE) expand uniformly under UV light due to photodimerization. This controlled expansion in nanostructures, unlike bulk crystals, suggests potential for nanoscale mechanical motion.
Area of Science:
- Materials Science
- Organic Chemistry
- Nanotechnology
Background:
- Organic crystals can undergo photochemical reactions.
- Nanostructure properties differ significantly from bulk materials.
- Photodimerization is a known photochemical process.
Purpose of the Study:
- To synthesize and characterize 9-tert-butylanthroate (9-TBAE) nanorods.
- To investigate the effect of UV light on 9-TBAE nanorods.
- To explore the potential of organic nanostructures for photochemical energy conversion.
Main Methods:
- Synthesis of nanorods using an Al2O3 template and solvent annealing.
- UV irradiation to induce photodimerization.
- Characterization using transmission electron microscopy (TEM) and atomic force microscopy (AFM).
- X-ray crystallography of monomer and photodimer.
Main Results:
- Uniform 15% expansion along the nanorod axis upon UV-induced [4+4] photodimerization.
- Nanorods maintained structural integrity, unlike random 9-TBAE crystals which disintegrated.
- Evidence of a crystal-to-crystal photoreaction mechanism leading to increased molecular volume.
- High surface-to-volume ratio in nanorods likely facilitates strain relief.
Conclusions:
- Organic nanostructures can undergo controlled photochemical expansion.
- Photochemical energy can be converted into mechanical motion at the nanoscale.
- The strain relief in nanorods is crucial for maintaining structural integrity during photoreaction.

