Synfacts 2008(10): 1044-1044  
DOI: 10.1055/s-2008-1078034
Synthesis of Materials and Unnatural Products
© Georg Thieme Verlag Stuttgart ˙ New York

Rapidly Switching Photochromic Dyes

Contributor(s):Timothy M. Swager, Rebecca R. Parkhurst
K. Fujita, S. Hatano, D. Kato, J. Abe*
Aoyama Gakuin University, Kanagawa, Japan
Photochromism of a Radical Diffusion-Inhibited Hexaarylbiimidazole Derivative with Intense Coloration and Fast Decoloration Performance
Org. Lett.  2008,  10:  3105-3108  
Further Information

Publication History

Publication Date:
22 September 2008 (online)


Significance

The authors report the design and synthesis of a new photochromic radical diffusion-inhibited hexaarylbiimidazole. By introducing one naphthalene moiety to create a heterodimer, they have expanded the range of absorption to include all visible light. Upon UV irradiation the colorless compound turns green with a thermal bleaching rate of t1/2 = 260 ms at 295 K such that decolor­ation occurs faster than diffusion of the colored species.

Comment

There are many potential applications for organic photochromic compounds including ­lithography and optical information processing. To be useful it is important that these compounds can switch rapidly between the colored and colorless states for many cycles. The authors use rational design to improve both of these properties and demonstrate the utility of organic synthesis in the field of photochromic dyes.