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      Photoswitchable gel assembly based on molecular recognition

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          Abstract

          The formation of effective and precise linkages in bottom-up or top-down processes is important for the development of self-assembled materials. Self-assembly through molecular recognition events is a powerful tool for producing functionalized materials. Photoresponsive molecular recognition systems can permit the creation of photoregulated self-assembled macroscopic objects. Here we demonstrate that macroscopic gel assembly can be highly regulated through photoisomerization of an azobenzene moiety that interacts differently with two host molecules. A photoregulated gel assembly system is developed using polyacrylamide-based hydrogels functionalized with azobenzene (guest) or cyclodextrin (host) moieties. Reversible adhesion and dissociation of the host gel from the guest gel may be controlled by photoirradiation. The differential affinities of α-cyclodextrin or β-cyclodextrin for the trans-azobenzene and cis-azobenzene are employed in the construction of a photoswitchable gel assembly system.

          Abstract

          Self-assembly through molecular recognition events is used in the production of functionalized materials. This study shows that macroscopic gel assembly can be regulated through photoisomerization of an azobenzene moiety that interacts differently with two host molecules.

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          Most cited references12

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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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            Polymeric rotaxanes.

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              Mechanical twisting of a guest by a photoresponsive host.

              Molecular analogues of a variety of mechanical devices such as shuttles, brakes, unidirectional rotors and tweezers have been created. But these 'molecular machines' have not yet been used to mechanically manipulate a second molecule in a controlled and reversible manner. Here we show that light-induced scissor-like conformational changes of one molecule can give rise to mechanical twisting of a non-covalently bound guest molecule. To realize this coupling of molecular motions, we use a previously designed system: a ferrocene moiety with an azobenzene strap, each end of which is attached to one of the two cyclopentadienyl rings of the ferrocene unit, acts as a pivot so that photoisomerization of the strap rotates the ferrocene rings relative to each other and thereby also changes the relative position of two 'pedal' moieties attached to the ferrocene rings. We translate this effect into intermolecular coupling of motion by endowing the pedals with binding sites, which allow the host system to form a stable complex with a bidentate rotor molecule. Using circular dichroism spectroscopy, we show that the photoinduced conformational changes of the host are indeed transmitted and induce mechanical twisting of the rotor molecule. This design concept, which significantly extends the successful coupling of motion beyond the intramolecular level seen in synthetic allosteric receptors, might allow for the remote control of molecular events in larger interlocked molecular systems.
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                Author and article information

                Journal
                Nat Commun
                Nature Communications
                Nature Pub. Group
                2041-1723
                03 January 2012
                : 3
                : 603
                Affiliations
                [1 ]simpleDepartment of Macromolecular Science, Graduate School of Science, Osaka University, Toyonaka , Osaka 560-0043, Japan.
                [2 ]simpleJapan Science and Technology Agency (JST), Core Research for Evolutional Science and Technology (CREST), Chiyoda-ku , Tokyo 102-0076, Japan.
                Author notes
                Article
                ncomms1617
                10.1038/ncomms1617
                3272571
                22215078
                ceda4ab4-a203-4484-ab91-7a8a23149e71
                Copyright © 2012, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.

                This work is licensed under a Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

                History
                : 29 July 2011
                : 28 November 2011
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