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      Novel photo-switching using azobenzene functional materials

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      Journal of Photochemistry and Photobiology A: Chemistry
      Elsevier BV

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          Photomechanics: directed bending of a polymer film by light.

          Polymer solutions and solids that contain light-sensitive molecules can undergo photo-contraction, whereby light energy is converted into mechanical energy. Here we show that a single film of a liquid-crystal network containing an azobenzene chromophore can be repeatedly and precisely bent along any chosen direction by using linearly polarized light. This striking photomechanical effect results from a photoselective volume contraction and may be useful in the development of high-speed actuators for microscale or nanoscale applications, for example in microrobots in medicine or optical microtweezers.
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            Photoinduced motions in azo-containing polymers.

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              Optical switching and image storage by means of azobenzene liquid-crystal films.

              Liquid crystals are promising materials for optical switching and image storage because of their high resolution and sensitivity. Azobenzene liquid crystals (LCs) have been developed, in which azobenzene moieties play roles as both mesogens and photosensitive chromophores. Azobenzene LC films showed a nematic phase in trans isomers and no LC phase in cis isomers. Trans-cis photoisomerization of azobenzene with a laser pulse resulted in a nematic-to-isotropic phase transition with a rapid optical response of 200 microseconds.
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                Author and article information

                Journal
                Journal of Photochemistry and Photobiology A: Chemistry
                Journal of Photochemistry and Photobiology A: Chemistry
                Elsevier BV
                10106030
                September 2006
                September 2006
                : 182
                : 3
                : 250-261
                Article
                10.1016/j.jphotochem.2006.04.021
                51b8c9c9-2d8f-489a-a59f-4a53c6262833
                © 2006

                http://www.elsevier.com/tdm/userlicense/1.0/

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