Bardeen Research Group

Department of Chemistry | University of California @ Riverside | 501 Big Springs Road | 127-131 CS-1

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Bardeen Research Group
University of California, Riverside * Department of Chemistry
501 Big Springs Rd * Riverside, CA 92521, USA
Phone: +1.951.827.2723 * Fax: +1.951.827.4713 * Email: christob@ucr.edu

Our main activities are

EDMAAM
Spotlight:Research

Photomechanical Molecular
Crystal Nanowires

  A novel anthracene-9-(1,3-butadiene) derivative, dimethyl-2(3-(anthracen-9-yl)allylidene)malonate (DMAAM) has been synthesized.  We have studied its solid-state structure and reactivity and show that a pulse of visible light can induce a dramatic curling motion in crystalline nanowires. 

Considerable effort has been devoted to making static coiled nanowires, usually by changing extrinsic factors like the nanowire’s surface chemistry or solvent environment. The coiling observed in this paper is qualitatively different, since it relies on intrinsic chemical changes taking place inside the wire itself, namely the E↔Z photoisomerization.  This motion occurs under uniform illumination conditions and illustrates how a molecular crystal nanostructure can undergo a nontrivial and possibly useful geometry change after photoexcitation.

The photoinduced motion is observed for nanowires composed of either (E)- or (Z)-DMAAM and may involve interactions between crystalline reactant and amorphous product phases. 

 

Snapshots showing coiling of an (E)-DMAAM nanowire after ~1 second of light exposure at time 0 s. Scale bars: 10 µm.

This heterometry mechanism, arising from a solid-state unimolecular photochemical reaction, could provide a way to design novel photoresponsive structures that rapidly change their extent in response to visible light.

For more information, check out our paper
Photo-induced Curling of Organic Molecular Crystal Nanowires.
Taehyung Kim et al.
Angewandte
Chemie, in press May 2013