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      Control over molecular motion using the cistrans photoisomerization of the azo group

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          Summary

          Control over molecular motion represents an important objective in modern chemistry. Aromatic azobenzenes are excellent candidates as molecular switches since they can exist in two forms, namely the cis ( Z) and trans ( E) isomers, which can interconvert both photochemically and thermally. This transformation induces a molecular movement and a significant geometric change, therefore the azobenzene unit is an excellent candidate to build dynamic molecular devices. We describe selected examples of systems containing an azobenzene moiety and their motions and geometrical changes caused by external stimuli.

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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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            Cyclic polyethers and their complexes with metal salts

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              Azobenzene photoswitches for biomolecules.

              The photoisomerization of azobenzene has been known for almost 75 years but only recently has this process been widely applied to biological systems. The central challenge of how to productively couple the isomerization process to a large functional change in a biomolecule has been met in a number of instances and it appears that effective photocontrol of a large variety of biomolecules may be possible. This critical review summarizes key properties of azobenzene that enable its use as a photoswitch in biological systems and describes strategies for using azobenzene photoswitches to drive functional changes in peptides, proteins, nucleic acids, lipids, and carbohydrates (192 references). This journal is © The Royal Society of Chemistry 2011
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                Author and article information

                Contributors
                Role: Guest Editor
                Journal
                Beilstein J Org Chem
                Beilstein J Org Chem
                Beilstein Journal of Organic Chemistry
                Beilstein-Institut (Trakehner Str. 7-9, 60487 Frankfurt am Main, Germany )
                1860-5397
                2012
                12 July 2012
                : 8
                : 1071-1090
                Affiliations
                [1 ]Instituto de Química Orgánica General, Centro Superior de Investigaciones Científicas (CSIC), C/ Juan de la Cierva, 3, 28006, Madrid, Spain
                [2 ]Departmento de Química Orgánica, Facultad de Ciencias, Universidad Autónoma de Madrid, 28049, Madrid, Spain
                Article
                10.3762/bjoc.8.119
                3458724
                23019434
                65d548d4-f84f-436f-9f3c-d7dfa58dd4f7
                Copyright © 2012, Merino and Ribagorda; licensee Beilstein-Institut.

                This is an Open Access article under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: ( http://www.beilstein-journals.org/bjoc)

                History
                : 16 March 2012
                : 21 June 2012
                Categories
                Review
                Chemistry
                Organic Chemistry

                Organic & Biomolecular chemistry
                azobenzenes,molecular switches,nanomachines,photoisomerization

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