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      Photoswitchable nonlinear optical properties of metal complexes

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          Abstract

          Incorporating photosensitive molecules into the organic/inorganic hybrid materials can contribute to forming photoresponsive systems.

          Abstract

          Incorporating photosensitive molecules into the organic/inorganic hybrid materials can contribute to forming photoresponsive systems. The second/third-order nonlinear optical properties can be changed via external light stimulation at an appropriate wavelength. The photochromic metal complexes appear to be superior promising materials in the domain of photoswitchable nonlinear optics (NLO). Thus, the purpose of this review is to examine current progress of metal complexes in the field of photoswitchable NLO materials and provide perspectives for the future. The overview includes the second-order and third-order NLO photoswitches and NLO properties of metal complexes. Combined with the characteristics of pyrene and stilbazolium groups, we describe a new type of photoswitchable NLO materials. The rapidly increasing investigations in this domain suggest that NLO photoswitches of metal complexes would play a critical role for inspiring applications in the future.

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          Most cited references86

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          A Powder Technique for the Evaluation of Nonlinear Optical Materials

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            Pyrene-based materials for organic electronics.

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              Rapid and reversible shape changes of molecular crystals on photoirradiation.

              The development of actuators based on materials that reversibly change shape and/or size in response to external stimuli has attracted interest for some time. A particularly intriguing possibility is offered by light-responsive materials, which allow remote operation without the need for direct contact to the actuator. The photo-response of these materials is based on the photoisomerization of constituent molecules (typically trans-cis isomerization of azobenzene chromophores), which gives rise to molecular motions and thereby deforms the bulk material. This effect has been used to create light-deformable polymer films and gels, but the response of these systems is relatively slow. Here we report that molecular crystals based on diarylethene chromophores and with sizes ranging from 10 to 100 micrometres exhibit rapid and reversible macroscopic changes in shape and size induced by ultraviolet and visible light. We find that on exposure to ultraviolet light, a single crystal of 1,2-bis(2-ethyl-5-phenyl-3-thienyl)perfluorocyclopentene changes from a square shape to a lozenge shape, whereas a rectangular single crystal of 1,2-bis(5-methyl-2-phenyl-4-thiazolyl)perfluorocyclopentene contracts by about 5-7 per cent. The deformed crystals are thermally stable, and switch back to their original state on irradiation with visible light. We find that our crystals respond in about 25 microseconds (that is, about five orders of magnitude faster than the response time of the azobenzene-based polymer systems) and that they can move microscopic objects, making them promising materials for possible light-driven actuator applications.
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                Author and article information

                Contributors
                Journal
                ICHBD9
                Dalton Transactions
                Dalton Trans.
                Royal Society of Chemistry (RSC)
                1477-9226
                1477-9234
                2018
                2018
                : 47
                : 1
                : 13-22
                Affiliations
                [1 ]College of Chemistry and Molecular Engineering
                [2 ]Zhengzhou University
                [3 ]Zhengzhou
                [4 ]P. R. China
                [5 ]College of Chemistry and Chemical Engineering and Henan Key Laboratory of Function Oriented Porous Materials
                Article
                10.1039/C7DT03989A
                3edf128f-e640-4fbe-b6d7-217633a14eb9
                © 2018

                http://rsc.li/journals-terms-of-use

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